Lupus Annals MI 2013

Systemic Lupus
Erythematosus
Physician Writer
Marianthi Kiriakidou MD
Section Editors
Deborah Cotton, MD, MPH
Darren Taichman, MD, PhD
Sankey Williams, MD
Screening
page ITC4-2
Diagnosis
page ITC4-3
Treatment
page ITC4-6
Tool Kit
page ITC4-14
Patient Information
page ITC4-15
CME Questions
page ITC4-16
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CME Objective: To review current evidence for the screening, diagnosis, and treatment of systemic lupus erythematosus.
The information contained herein should never be used as a substitute for clinical
judgment.
2013 American College of Physicians
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In theClinic
In the Clinic
ystemic lupus erythematosus (SLE, lupus) is a condition in which the

immune system attacks healthy cells and tissues throughout the body.
Immune system activation in SLE is characterized by exaggerated
B-cell and T-cell responses and loss of immune tolerance against self antigens. Production and defective elimination of antibodies, circulation and
tissue deposition of immune complexes, and complement and cytokine activation contribute to clinical manifestations that range from mild fatigue and
joint pain to severe, life-threatening organ damage.
S
1. Demas KL, Costenbader KH. Disparities
in lupus care and
outcomes. Curr Opin
Rheumatol.
2009;21:102-9.
[PMID: 19339919]
2. Bernatsky S, Boivin JF,
Joseph L, et al. Mortality in systemic lupus erythematosus.
Arthritis Rheum.
2006;54:2550-7.
[PMID: 16868977]
3. Sestak AL, Frnrohr
BG, Harley JB, et al.
The genetics of systemic lupus erythematosus and implications for targeted
therapy. Ann Rheum
Dis. 2011;70 Suppl
1:i37-43.
[PMID: 21339217]
4. Deng Y, Tsao BP. Genetic susceptibility to
systemic lupus erythematosus in the
genomic era. Nat Rev
Rheumatol.
2010;6:683-92.
[PMID: 21060334]
5. Arbuckle MR, McClain
MT, Rubertone MV, et
al. Development of
autoantibodies before the clinical onset
of systemic lupus erythematosus. N Engl J
Med. 2003;349:152633. [PMID: 14561795]
6. Seibold JR, Wechsler
LR, Cammarata RJ. LE
cells in intermittent
hydrarthrosis [Letter].
Arthritis Rheum.
1980;23:958-9.
[PMID: 6157396]
7. Ball EM, Bell AL. Lupus
arthritis-do we
have a clinically useful classification?
Rheumatology (Oxford). 2012;51:771-9.
[PMID: 22179731]
8. Patel P, Werth V. Cutaneous lupus erythematosus: a review.
Dermatol Clin.
2002;20:373-85, v.
[PMID: 12170873]
9. Alarcn GS, Friedman
AW, Straaton KV, et al.
Systemic lupus erythematosus in three
ethnic groups: III. A
comparison of characteristics early in the
natural history of the
LUMINA cohort. LUpus in MInority populations: NAture vs.
Nurture. Lupus.
1999;8:197-209.
[PMID: 10342712]
10. Chang AY, Werth VP.
Treatment of cutaneous lupus. Curr
Rheumatol Rep.
2011;13:300-7.
[PMID: 21503694]
Because the symptoms of SLE vary widely and the condition often goes
undiagnosed, it is unclear how many people in the United States have the
disease. It is diagnosed 9 times more often in women than in men, which
implies pathogenic mechanisms more prevalent in women. These mechanisms, which probably involve effects of sex chromosomes, specific genes,
and hormones, have not been completely elucidated. SLE is more common
and more severe in African American women, Hispanic women, and those
of other ethnic minorities (1).
Although there is no cure for SLE, it can be effectively managed with medications; however, mortality is higher in patients with SLE than in the general population. The overall standardized mortality ratio (SMR) (ratio of
deaths observed to deaths expected for an age group) for SLE is 2.4. Higher
risk for death is associated with female sex, younger age, shorter SLE duration, and African American race (2).
Screening
Which patients are at elevated

risk for lupus?
Evidence to determine whether
people may be at risk for lupus
because of specific genes is insufficient. Early genetic studies,
driven by the observation of familial aggregation and high concordance in monozygotic twins,
have implicated genes for HLA
and early complement components (3). A few rare, single-gene
risk factors have been linked to
SLE. For example, C1, C2, or C4
genetic deficiencies can cause lupus but account for just 12% of
cases (3). Recent genome-wide
association studies have linked
more than 30 gene polymorphisms to lupus (4). However, the
functional significance of these
variants and their potential implication to SLE pathogenesis
remain largely unknown. In addition, sex chromosome genes,
and possibly sex hormones and
environmental influences, may
contribute to immune system
dysfunction in genetically predisposed individuals.
ITC4-2
Annals of Internal Medicine
In the Clinic
Should clinicians screen

asymptomatic patients for lupus if
they are at increased risk?
Most experts do not recommend
screening asymptomatic persons
for lupus, even those with a family history. Nevertheless, the immunologic test for antinuclear
antibody (ANA) is often used for
SLE screening even though it
produces many false-positive results. ANA is detected in 35% of
healthy individuals or patients
with other autoimmune or infectious diseases. Furthermore, serologic evidence of ANAs, which
indicates immune system activation, may precede the clinical
manifestations required for diagnosis by 3 to 9 years (5). No evidence suggests that treating to
modulate the immune system
during this clinically silent period can stop or delay lupus development.
1 October 2013
Screening... Single-gene mutations causing SLE are rare. Although numerous gene
variants have been linked to lupus, current evidence is insufficient to support
screening for these variants. ANA testing in asymptomatic persons is not useful
because immune reaction to nuclear antigens is not SLE-specific, can be detected
in healthy individuals, and may precede SLE manifestations by many years.
CLINICAL BOTTOM LINE
What other clinical manifestations

should clinicians look for in
potential cases of lupus?
Systemic lupus may present in
many other ways. Although fever,
rash, and arthritis are the classic
initial symptoms, abrupt onset with
target-organ involvement is also
quite common, particularly in
11. Vil LM, Alarcn GS,

McGwin G Jr, et al;
Lumina Study
Group. Systemic lupus erythematosus
in a multiethnic US
cohort, XXXVII: association of lymphopenia with clinical
manifestations, serologic abnormalities,
disease activity, and
damage accrual.
Arthritis Rheum.
2006;55:799-806.
[PMID: 17013840]
12. Durn S, Apte M,
Alarcn GS, et al; Lumina Study Group.
Features associated
with, and the impact
of, hemolytic anemia
in patients with systemic lupus erythematosus: LX, results
from a multiethnic
cohort. Arthritis
Rheum.
2008;59:1332-40.
[PMID: 18759263]
13. Bomback AS, Appel
GB. Updates on the
treatment of lupus
nephritis. J Am Soc
Nephrol.
2010;21:2028-35.
[PMID: 21051743]
14. Cervera R, Khamashta MA, Font J, et al;
European Working
Party on Systemic
Lupus Erythematosus. Morbidity and
mortality in systemic
lupus erythematosus during a 10-year
period: a comparison of early and late
manifestations in a
cohort of 1,000 patients. Medicine (Baltimore). 2003;82:299308.
[PMID: 14530779]
15. Mok CC, Kwok RC,
Yip PS. Effect of renal
disease on the standardized mortality
ratio and life expectancy of patients
with systemic lupus
erythematosus.
Arthritis Rheum.
2013;65:2154-60.
[PMID: 23754671]
16. Kamen DL, Strange
C. Pulmonary manifestations of systemic lupus erythematosus. Clin Chest
Med. 2010;31:47988. [PMID: 20692540]
17. Peponis V, Kyttaris
VC, Tyradellis C, et al.
Ocular manifestations of systemic lupus erythematosus:
a clinical review. Lupus. 2006;15:3-12.
[PMID: 16482739]
ITC4-3
Diagnosis
What symptoms or physical
examination findings should
prompt clinicians to consider a
diagnosis of lupus?
The initial presentation of lupus often mimics a viral syndrome. Such
constitutional symptoms as weight
loss, fatigue, and low-grade fever are
common and may be accompanied
by arthralgias or arthritis. Arthritis
in lupus is characterized by prolonged morning stiffness and mild
to moderate joint swelling. It is
nonerosive, may be symmetric or
asymmetric, and may affect large or
small joints. Large effusions are not
as common in lupus as in rheumatoid arthritis, and the synovial fluid
is not as inflammatory (6). Joint
deformities are not frequent in lupus. Jaccoud arthropathy, which
may include reducible ulnar deviation, swan neck deformities, or
z-shaped thumb, is present in
2.84.3% of patients (7). When
constitutional symptoms with
arthralgias or arthritis are not accompanied by other characteristic
manifestations of lupus, such as
photosensitive skin rash on the
face, neck, or extremities, it is appropriate to conduct a clinical and
laboratory evaluation for infection
before trying to establish a diagnosis of SLE.
Cutaneous manifestations are common and may occur in up to 70%
of patients (8). They are categorized as acute, subacute, or chronic.
Acute cutaneous lupus consists of
indurated or flat erythematous
lesions on the malar eminences,
scalp, arms, hands, neck, and chest.
1 October 2013
The malar rash may be confused

with rosacea, drug eruption, or
polymorphous light eruption, but
skin biopsy is rarely necessary when
other clinical manifestations and
serologic evidence consistent with
SLE are present. Subacute cutaneous lupus consists of annular
lesions that may coalesce into a
polycyclic (overlapping ring-shaped)
rash or papulosquamous lesions
that do not scar and are distributed
where light exposure is most frequent. It is often associated with
anti-SSA antibodies. Chronic cutaneous lupus includes discoid lupus
and other rare subsets, such as lupus
panniculitis, hypertrophic lupus erythematosus (characterized by verrucous lesions), tumid lupus or lupus
tumidus (smooth, shiny, red-violet
plaques usually on the head and
neck), and chilblain lupus (purplishblue lesions on the fingers, toes, or
ears). Discoid lupus is the most
common form of the chronic cutaneous disease and is characterized
by scarring indurated plaques that
resolve with significant depigmentation. Although acute cutaneous lupus is nearly always associated with
systemic lupus, discoid lupus is infrequently (35%) associated with
systemic disease (9).
In the Clinic
18. Hochberg MC. Updating the American

College of Rheumatology revised criteria for the classification of systemic
lupus erythematosus [Letter]. Arthritis
Rheum.
1997;40:1725.
[PMID: 9324032]
19. Petri M, Orbai AM,
Alarcn GS, et al.
Derivation and validation of the Systemic Lupus International Collaborating
Clinics classification
criteria for systemic
lupus erythematosus. Arthritis Rheum.
2012;64:2677-86.
[PMID: 22553077]
20. Sun S, Rao NL, Venable J, Thurmond R,
Karlsson L. TLR7/9
antagonists as therapeutics for immunemediated inflammatory disorders.
Inflamm Allergy
Drug Targets.
2007;6:223-35.
[PMID: 18220957]
21. Ben-Zvi I, Kivity S,
Langevitz P, Shoenfeld Y. Hydroxychloroquine: from
malaria to autoimmunity. Clin Rev Allergy Immunol.
2012;42:145-53.
[PMID: 21221847]
22. Farrell DF. Retinal
toxicity to antimalarial drugs: chloroquine and hydroxychloroquine: a
neurophysiologic
study. Clin Ophthalmol. 2012;6:377-83.
[PMID: 22457587]
23. Mackworth-Young
CG, David J, Morgan
SH, et al. A double
blind, placebo controlled trial of intravenous methylprednisolone in systemic
lupus erythematosus. Ann Rheum Dis.
1988;47:496-502.
[PMID: 3289511]
24. Albert DA, Hadler
NM, Ropes MW.
Does corticosteroid
therapy affect the
survival of patients
with systemic lupus
erythematosus?
Arthritis Rheum.
1979;22:945-53.
[PMID: 475873]
25. Edwards JC, Snaith
ML, Isenberg DA. A
double blind controlled trial of
methylprednisolone
infusions in systemic
lupus erythematosus using individualised outcome assessment. Ann
Rheum Dis.
1987;46:773-6.
[PMID: 3318723]
Hispanics (61%) and African

Americans (45%), as compared
with white patients (41%) (10).
SLE should be considered when
patients, particularly women of reproductive age, present with hematologic, renal, respiratory, or central
nervous system (CNS) manifestations, especially hematologic findings, such as thrombocytopenia,
leukopenia, lymphopenia, or anemia; renal findings, such as hematuria, proteinuria, cellular casts, or
elevated serum creatinine; respiratory symptoms, such as cough, dyspnea, hemoptysis, or pleuritic pain;
or CNS signs, such as headache,
photophobia, or focal neurologic
deficits.
Hematologic manifestations
Cytopenias are common in patients

with lupus, and moderate-to-severe
lymphopenia is associated with
high disease activity and organ
damage (11). Hemolytic anemia is
uncommon and usually associated
with disease onset, thrombocytopenia, and African American
ethnicity (12).
Renal manifestations
Renal involvement is a common

target-organ manifestation; it has
a poor prognosis due to the high
risk for organ failure. Up to
50% of SLE patients have some
evidence of renal disease at presentation (13). SLE nephritis is associated with a worse prognosis for
10-year survival than the nonrenal
disease (14). Compared with the
general population, life expectancy
is reduced by 12.4, 15.1, and 23.7
years in lupus patients, those with
renal disease, and those with renal
damage, respectively (15).
affecting 3050% of patients (16).

Lupus pleuritis should be diagnosed only after an analysis of
pleural fluid and an evaluation for
other causes of pleural effusion,
such as infection, pulmonary embolism, liver disease, heart disease,
and cancer. Bronchoscopy for bacterial, mycobacterial, fungal, and viral
cultures may be indicated. Vascular
involvement may cause diffuse
alveolar hemorrhage, pulmonary
hypertension, or thromboembolic
disease. Parenchymal damage is less
common and may be the result of
interstitial lung disease, acute pneumonitis, or bronchiolitis obliterans
with organizing pneumonia. Acute
lupus pneumonitis is rare and carries a high mortality risk. Infection
and pulmonary embolism must always be excluded in patients with
suspected lupus pneumonitis.
Neuropsychiatric manifestations
Neuropsychiatric SLE manifestations may be caused by vasculopathy,

autoantibodies, and inflammatory
mediators and include headache,
aseptic meningitis, vasculitis, movement disorder, seizure disorder,
cognitive dysfunction, psychosis,
demyelinating disease, myelopathy,
autonomic disorder, and peripheral
neuropathy.
Ocular manifestations
Ocular manifestations include keratoconjuctivitis sicca (with or without

the Sjogren syndrome), keratitis,
episcleritis, scleritis, uveitis, retinal
vasculitis, occlusion of the retinal
artery or vein, retinopathy, and numerous other less common manifestations (17).
Gastrointestinal manifestations
Involvement of the respiratory system may be primary or secondary.

Presenting symptoms and the response to treatment vary, depending on the affected anatomical site.
Pleuritis is the most common
respiratory SLE manifestation,
Gastrointestinal symptoms may

include anorexia, nausea, vomiting, abdominal pain, and diarrhea.
Other causes of abdominal pain in
lupus are mesenteric vasculitis and
hepatobiliary disease. Rare gastrointestinal complications include
intestinal pseudo-obstruction,
protein-losing enteropathy, and
ITC4-4
Respiratory involvement
In the Clinic
1 October 2013
pancreatitis. Immunocompromised
lupus patients are also prone to
enteritis from cytomegalovirus or
salmonella infection.
Lupus is a multiorgan disease that
can mimic infectious diseases, cancer, and other autoimmune conditions. Table 1 lists the American
College of Rheumatology (ACR)
classification criteria for SLE (18).
These criteria facilitate a systematic approach to diagnosis by focusing on the most common SLE
manifestations. Four of the 11 criteria are required for classification
of systemic lupus. Although intended to assist in classification,
the ACR criteria offer a highly
sensitive and specific tool for
diagnosing SLE, based on objective

disease manifestations. However,
patients with mild disease may be
missed. In 2012 the Systemic Lupus International Collaborating
Clinics revised the ACR classification criteria, increasing the sensitivity but not the specificity of
detecting SLE compared with the
1997 ACR criteria (19).
What laboratory tests should
clinicians use to diagnose lupus?
Clinicians should test for ANA,
and if the result is positive, followup testing for antigen-specific
ANAs, such as those targeting
double-stranded DNA (dsDNA) or
ribonucleoprotein complexes
(Ro/SSA, La/SSB, Smith, and
Table 1. American College of Rheumatology Classification Criteria for SLE*

Criterion
Definition
Malar rash
Flat or raised erythema over the malar eminences, sparing the nasolabial folds
Discoid rash
Erythematous raised patches or atrophic scarring (older lesions)
Photosensitivity
Skin rash as a result of unusual reaction to sunlight
Oral ulcers
Usually painless oral or nasopharyngeal ulcerations, observed by physician
Arthritis
Nonerosive arthritis, involving 2 or more peripheral joints characterized by tenderness and

swelling
Serositis
Pleuritis: Convincing history of pleuritic pain or rubbing heard by physician, or evidence of

pleural effusion
Pericarditis: Documented by electrocardiogram, or rub or evidence of pericardial effusion
Renal disorder
Persistent proteinuria >0.5 g/d or >3 on dipstick

Cellular casts red cell, hemoglobin, granular, tubular, or mixed
Neurologic disorder
Seizures (in the absence of offending drugs or metabolic derangement)

Psychosis (in the absence of offending drugs or metabolic derangement)
Hematologic disorder
Hemolytic anemia: with reticulocytosis

Leukopenia: <4000/mm on 2 or more occasions
Lymphopenia: <1500/mm on 2 or more occasions
Thrombocytopenia: <100 000/mm in the absence of offending drugs
Immunologic disorder
Anti-DsDNA
Anti-Smith antibodies
Antiphospholipid antibodies based on an abnormal serum level of IgG or IgM anticardiolipin
antibodies, positive test result for lupus anticoagulant using a standard method, or falsepositive serologic test result for syphilis known to be positive for at least 6 mo and confirmed
as false-positive by Treponema pallidum immobilization or fluorescent treponemal antibody
absorption tests
Antinuclear antibody
Detected by immunofluoresence (or equivalent assay) in the absence of drugs known to be

associated with drug-induced SLE
*From reference 18.
1 October 2013
In the Clinic
ITC4-5
26. Badsha H, Kong KO,

Lian TY, et al. Lowdose pulse methylprednisolone for systemic lupus
erythematosus flares
is efficacious and
has a decreased risk
of infectious complications. Lupus.
2002;11:508-13.
[PMID: 12220105]
27. Buttgereit F, da Silva
JA, Boers M, et al.
Standardised
nomenclature for
glucocorticoid
dosages and glucocorticoid treatment
regimens: current
questions and tentative answers in
rheumatology. Ann
Rheum Dis.
2002;61:718-22.
[PMID: 12117678]
28. Da Silva JA. Safety of
glucocorticoids clinical trials. Clin
Exp Rheumatol.
2011;29:S99-103.
[PMID: 22018193]
29. Carneiro JR, Sato EI.
Double blind, randomized, placebo
controlled clinical
trial of methotrexate
in systemic lupus
erythematosus. J
Rheumatol.
1999;26:1275-9.
[PMID: 10381042]
30. Islam MN, Hossain
M, Haq SA, et al. Efficacy and safety of
methotrexate in articular and cutaneous manifestations of systemic
lupus erythematosus. Int J Rheum Dis.
2012;15:62-8.
[PMID: 22324948]
31. Fortin PR, Abrahamowicz M, Ferland D, et al; Canadian Network For
Improved Outcomes
in Systemic Lupus.
Steroid-sparing effects of methotrexate in systemic lupus
erythematosus: a
double-blind, randomized, placebocontrolled trial.
Arthritis Rheum.
2008;59:1796-804.
[PMID: 19035431]
32. Gourley MF, Austin
HA 3rd, Scott D, et al.
Methylprednisolone
and cyclophosphamide, alone or in
combination, in patients with lupus
nephritis. A randomized, controlled trial.
Ann Intern Med.
1996;125:549-57.
[PMID: 8815753]
Basic Investigations for SLE

Complete blood count
Direct Coombs test (indicated if
patients present with hemolytic
anemia and reticulocytosis)
Comprehensive metabolic panel
Erythrocyte sedimentation rate
C-reactive protein
Urinalysis
Serologic testing (ANA and if
positive, anti-DsDNA, antiSSA/SSB, anti-Smith/RNP antiphospholipid antibodies); a
negative ANA test is inconsistent
with the diagnosis of SLE
Complement C3 and C4
Creatine phosphokinase (indicated
in patients presenting with
muscle weakness)
33. Illei GG, Austin HA,

Crane M, et al. Combination therapy
with pulse cyclophosphamide
plus pulse methylprednisolone improves long-term renal outcome
without adding toxicity in patients with
lupus nephritis. Ann
Intern Med.
2001;135:248-57.
[PMID: 11511139]
34. Hochstadt A, Rozman Z, ZandmanGoddard G. [Mycophenolate mofetil
as a novel treatment
for lupus nephritis].
Harefuah.
2011;150:542-7, 550.
[PMID: 21800496]
35. Anderka MT, Lin AE,
Abuelo DN, et al. Reviewing the evidence for mycophenolate mofetil as a
new teratogen: case
report and review of
the literature. Am J
Med Genet A.
2009;149A:1241-8.
[PMID: 19441125]
36. Kamanamool N,
McEvoy M, Attia J, et
al. Efficacy and adverse events of mycophenolate mofetil
versus cyclophosphamide for induction therapy of lupus
nephritis: systematic
review and metaanalysis. Medicine
(Baltimore).
2010;89:227-35.
[PMID: 20616662]
37. Touma Z, Gladman
DD, Urowitz MB, et
al. Mycophenolate
mofetil for induction
treatment of lupus
nephritis: a systematic review and
metaanalysis. J
Rheumatol.
2011;38:69-78.
[PMID: 20952473]
RNP, which are collectively referred

to as extractable nuclear antigens)
should be done. The specificity of
anti ds-DNA antibodies for lupus is
>60%. Anti-Smith antibodies are
>90% specific for lupus; however,
they are detected in only about 30%
of lupus patients. The initial laboratory evaluation to assess disease activity and target-organ involvement
is described in the Box (Basic Investigations for SLE).
What other diagnoses should
clinicians consider?
The chronic fatigue syndrome and fibromyalgia may present with diffuse
musculoskeletal symptoms mimicking lupus, or may be secondary to
SLE. SLE can be excluded in the absence of inflammatory pain and negative results on serologic evaluation.
Rheumatoid arthritis is characterized
by symmetric, intensely inflammatory,
erosive arthritis (when advanced) and
positive results on rheumatoid factor
or anti-CCP antibody testing.
Such drugs as procainamide, hydralazine, minocycline, isoniazide,
and tumor necrosis factor inhibitors
can cause drug-induced lupus, a clinical syndrome resembling SLE characterized by fever, serositis, arthritis,
and rash. Antihistone antibodies are
detected in approximately 75% of patients; however, they can also be seen
in SLE and are not pathognomonic.
Anti-dsDNA, or antibodies to
extractable nuclear antigens, are rare

in drug-induced lupus, and symptoms usually abate within days or
weeks after drug discontinuation.
Small- or medium-vessel vasculitides,
thrombotic thrombocytopenic purpura, and viral arthritis, as seen in
parvovirus infection and HIV/AIDS,
can also mimic SLE. Differential diagnosis relies on laboratory studies,
detection of viral serologies, and tissue histopathology. Hematopoietic
cancer and malignant lymphoproliferative syndromes may present with
positive ANA, anemia, low-grade
fever, pleural effusions, and lymphadenopathy and can be misdiagnosed as lupus.
When should clinicians consider
consulting with a rheumatologist
or other specialist for diagnosing
patients with possible lupus?
Clinicians should consult a
rheumatologist in all patients when
clinical manifestations and serologic studies suggest SLE. Evidence of
renal, pulmonary, CNS, ocular, or
gastrointestinal disease necessitates
a coordinated, multidisciplinary approach with the help of appropriate
specialists. The goal of care is a
timely, accurate diagnosis; effective
treatment of acute disease; appropriate monitoring and dose adjustment; and early introduction of a
steroid-sparing regimen.
Diagnosis... Lupus is a multisystem disease that often presents as a diagnostic challenge because it can include cutaneous, renal, respiratory, cardiovascular, CNS, and
gastrointestinal manifestations that characterize numerous other conditions. The ACR
classification criteria can be used to guide the diagnosis of systemic lupus.
Treatment
What medications are used to

treat lupus?
Clinicians use a broad range of medications to treat lupus, including
glucocorticoids, antimalarial agents,

and nonsteroidal anti-inflammatory
drugs (NSAIDs) (Table 2). Hydroxychloroquine prevents disease flares
ITC4-6
In the Clinic
1 October 2013
Table 2. Drug Treatment for SLE

Agent
Mechanism of Action
NSAIDs
Anti-inflammatory
Glucocorticoids
Anti-inflammatory effect
due to negative transcriptional
regulation of pro-inflammatory
genes
Low: 7 mg/d; medium:

>730 mg/d; high: >30
100 mg/d; very high:
>100 mg/d; pulse: 250 mg/d (27)
Fluid retention, diabetes mellitus,

hypertension, acne, myopathy,
hyperlipidemia, psychosis, avascular bone
necrosis, osteoporosis
Hydroxychloroquine
Immunomodulatory and
antithrombotic effect
200400 mg/d (orally)
Skin hyperpigmentation, retinal toxicity

(rare), myopathy with peripheral
neuropathy and cardiac myotoxicity
(extremely rare)
Mycophenolate mofetil
Inhibits lymphocyte proliferation

Up to 3000 mg/d (orally)
by inhibiting inosine monophosphate
dehydrogenase and de novo synthesis
of guanosine nucleotides; promotes
apoptosis of T-lymphocytes
Gastrointestinal intolerance, myelosuppression
Azathioprine
Metabolizes to 6-TG and 6-MMP

and inhibits DNA synthesis and cell
proliferation
50150 mg/d (orally)
Gastrointestinal intolerance, myelosuppression, hepatotoxicity
Methotrexate
Inhibits DNA synthesis and increases

release of adenosine
525 mg/wk (orally or subcutaneously)
Gastrointestinal intolerance, hepatotoxicity
Cyclophosphamide
Alkylating agent, promotes DNA

cross-linking and inhibits T- and
B-lymphocyte proliferation
Based on body surface area

and renal function (IV or oral
administration)
Hair loss, gastrointestinal toxicity, myelosuppression, hemorrhagic cystitis, bladder

cancer, gonadal suppression, infertility
Cyclosporine
Calcineurin inhibitor inhibits

T-lymphocyte proliferation and
expression or activation of proinflammatory cytokines
2.54.5 mg/kg/d (orally)
Nephrotoxicity, interaction with allopurinol,

hypertension, myelosuppression
Tacrolimus
Calcineurin inhibitor
23 mg/d (orally)
Nephrotoxicity, neurotoxicity, myocardial

hypertrophy, hyperkalemia, infection, cancer
Belimumab
Targets B-lymphocyte stimulator,

inhibits B-lymphocyte proliferation
and activation
Three 10 mg/kg doses given IV at

2-wk intervals and then 10 mg/kg
IV every mo
Hypersensitivity reaction, gastrointestinal

toxicity, myalgias, depression, migraine,
infection
Rituximab
Depletes CD20-expressing
B-lymphocytes
Two 1000 mg doses given IV at

2-wk intervals; may be repeated
every 6 mo
Infusion reaction, infection, progressive

multifocal leukoencephalopathy (rare)
and is considered the cornerstone of

SLE treatment. Glucocorticoids are
first-line agents for most SLE manifestations, with dosage and treatment
duration based on clinical experience
and consensus. Immunosuppressive
treatment in lupus nephritis is based
on histopathologic classifications.
Treatment of other lupus manifestations is based on sparse evidence
from clinical trials and clinical
experience and often requires
1 October 2013
Dosage
Common Side Effects
Gastritis, nephrotoxicity, fluid retention
immunosuppressive therapy and a

multidisciplinary approach.
How should clinicians initiate
therapy in a stable patient who is
not having a flare?
Hydroxychloroquine and other antimalarial agents have been used to
treat inflammatory arthritides for
at least 50 years (20). In addition
to preventing lupus relapses and
reducing the risk for congenital
38. Hahn BH, McMahon

MA, Wilkinson A, et
al; American College
of Rheumatology.
American College of
Rheumatology
guidelines for
screening, treatment, and management of lupus
nephritis. Arthritis
Care Res (Hoboken).
2012;64:797-808.
[PMID: 22556106]
ITC4-7
In the Clinic
39. Contreras G, Pardo V,

Leclercq B, et al. Sequential therapies
for proliferative lupus nephritis. N Engl
J Med. 2004;350:97180. [PMID: 14999109]
40. Dooley MA, Jayne D,
Ginzler EM, et al;
ALMS Group. Mycophenolate versus
azathioprine as
maintenance therapy for lupus nephritis. N Engl J Med.
2011;365:1886-95.
[PMID: 22087680]
41. Houssiau FA, DCruz
D, Sangle S, et al;
MAINTAIN Nephritis
Trial Group. Azathioprine versus mycophenolate mofetil
for long-term immunosuppression in
lupus nephritis: results from the MAINTAIN Nephritis Trial.
Ann Rheum Dis.
2010;69:2083-9.
[PMID: 20833738]
42. Moroni G, Doria A,
Mosca M, et al. A
randomized pilot trial comparing cyclosporine and azathioprine for
maintenance therapy in diffuse lupus
nephritis over four
years. Clin J Am Soc
Nephrol. 2006;1:92532. [PMID: 17699309]
43. Lee YH, Lee HS, Choi
SJ, et al. Efficacy and
safety of tacrolimus
therapy for lupus
nephritis: a systematic review of clinical
trials. Lupus.
2011;20:636-40.
[PMID: 21382917]
44. Merrill JT, Neuwelt
CM, Wallace DJ, et al.
Efficacy and safety of
rituximab in moderately-to-severely active systemic lupus
erythematosus: the
randomized, doubleblind, phase II/III systemic lupus erythematosus evaluation
of rituximab trial.
Arthritis Rheum.
2010;62:222-33.
[PMID: 20039413]
45. Rovin BH, Furie R, Latinis K, et al; LUNAR
Investigator Group.
Efficacy and safety of
rituximab in patients
with active proliferative lupus nephritis:
the Lupus Nephritis
Assessment with Rituximab study. Arthritis Rheum.
2012;64:1215-26.
[PMID: 22231479]
heart block in neonatal SLE, hydroxychloroquine has antithrombotic effects that are particularly
important to SLE patients with
antiphospholipid antibody-related
prothrombotic diathesis (21). Hydroxychloroquine is generally welltolerated, and the rare risk for
retinopathy is directly related to
the years of exposure to the drug
and the age of the patient.
In a study of 29 cases of antimalarial retinal toxicity over a period of 30 years, all
patients were older than 40 years and
had had exposure to the agents over
5 years (22).
Skin hyperpigmentation and rare

cases of neuromuscular or cardiac
toxicity have also been reported.
How should clinicians choose
therapy for a patient who is
having a flare?
Severe SLE manifestations, such as
lupus nephritis, alveolar hemorrhage, or CNS vasculitis, should be
treated with glucocorticoids administered intravenously (IV) in conjunction with immunosuppressive
medications. Glucocorticoids can be
gradually withdrawn once remission
is achieved. Oral prednisone or
methlyprednisolone is used for
arthritis, pleuropericarditis, cutaneous vasculitis, and uveitis.
Early studies demonstrated that
glucocorticoids could ameliorate
SLE, although subsequent controlled trials showed that the therapeutic effect was not sustained (23).
Early studies also linked glucocorticoids to improved survival in severe
SLE (24), but similar studies have
not been done for mild or moderate
disease. Current decisions about
glucocorticoid dosage and the
duration of treatment for specific
manifestations rely largely on clinical experience because too few clinical trials have been done.
3 daily doses of 100 mg (25). A more recent

randomized study showed that a dose of
1000 mg to 1500 mg over 3 days is as effective as doses ranging from 2000 mg to
5000 mg over 3 days and is associated
with a decreased risk for infections (26).
Significant overlap exists between

lupus manifestations and some
glucocorticoid complications, including osteoporosis, avascular
bone necrosis, myopathy, and psychosis. Furthermore, despite the
abundance of observational data
on glucocorticoid toxicity, evidence
from randomized, controlled clinical trials (RCTs) is limited. Table 2
summarizes the 2002 European
League Against Rheumatism recommendations on glucocorticoid
treatment (27). These recommendations define a low daily dose of
prednisone (or equivalent) as 7 mg.
Low doses are associated with relatively low risk for toxicity, although
monitoring for cushingoid symptoms, osteoporosis, cataracts,
glaucoma, hyperglycemia, and hypertension is probably justified.
Prolonged treatment with medium
to high doses carries a higher risk
for complications, including myopathy, psychosis, hyperlipidemia,
and atherosclerosis. However, the
prevalence and incidence of these
complications in different corticosteroid regimens are still unclear (28).
An early study comparing 100 mg

with 1000 mg of IV methylprednisolone
suggested that 3 daily doses of 1000 mg
did not have a significant advantage over
How should clinicians choose drug

therapy for cutaneous manifestations?
Commonly used topical treatments
for all forms of cutaneous lupus
(acute, subacute, and chronic)
include tacrolimus, R-salbutamol
pimecrolimus, clobetasol, betamethasone, or photoprotection. Their efficacy has been shown by RCTs. Such
trials have also shown efficacy of systemic hydroxychloroquine or chloroquine in cutaneous SLE. Although
other immunosuppressive or biologic
agents, such as methotrexate, mycophenolate mofetil, azathioprine,
and rituximab, may be used for cutaneous lupus, evidence is based on
ITC4-8
In the Clinic
1 October 2013
case reports or prospective, nonrandomized studies (9).

therapy for lupus arthritis?
Low-dose glucocorticoids and
antimalarials are first-line agents
for treating arthritis in lupus.
Methotrexate is often used for
arthritis or cutaneous disease, particularly in patients without other
systemic manifestations.
A double-blind RCT showed that methotrexate is effective in controlling cutaneous and
articular symptoms in SLE (29). These findings were also supported by a recent openlabel trial (30) and an RCT showing that
methotrexate can be used as a steroidsparing agent in SLE (31).
Methotrexate antagonizes folic acid

and inhibits purine and pyrimidine
synthesis. In addition, it increases
extracellular adenosine release.
Adenosine seems to be an important
mediator of the anti-inflammatory
effect of methotrexate.
How should clinicians choose and
dose drug therapy for lupus
nephritis?
Induction therapy
The indications for kidney biopsy

are in the Box: Indications for Kidney Biopsy in Patients With SLE;
the currently accepted classification
system for biopsy results are in the
Box: Histopathologic Classification
of Lupus Nephritis.
Class I or II lupus nephritis does
not require immunosuppressive
therapy. Class III or IV is treated
aggressively. Until recently, cyclophosphamide combined with intravenous glucocorticoids has been
the standard of care for induction
therapy of class III and IV lupus
nephritis. Cyclophosphamide is
an alkylating agent that promotes
DNA cross-linking and affects Tand B-cell proliferation and antibody production. It is usually dosed
according to total body surface area
and adjusted for decreased creatinine clearance. Cyclophosphamide
1 October 2013
toxicity includes hematologic, infectious, urologic, reproductive, and

rare pulmonary complications and
bladder, skin, myeloproliferative,
and oropharyngeal cancers. To date,
there is no definitive evidence from
clinical trials to guide clinicians on
the dose of glucocorticoids for induction therapy of lupus nephritis.
Current ACR recommendations
are based on expert opinion and
consensus.
Early open-label trials and RCTs showed
short-term efficacy of glucocorticoids for
treatment of lupus nephritis. Subsequently,
an RCT comparing cyclophosphamide to
glucocorticoids showed superiority of cyclophosphamide for induction therapy of
proliferative lupus nephritis. Nonresponse
was more common in the group treated with
IV glucocorticoids and the probability of
achieving remission was higher in the glucocorticoid plus cyclophosphamide group (32).
Long-term follow-up of the study participants indicated that an increase in creatinine
by 50% or 100% was less common in patients
receiving combination treatment (33).
Over the past decade, several studies

have shown efficacy of mycophenolate
mofetil for induction therapy in lupus
nephritis (3436). This drug is metabolized to mycophenolic acid, an inhibitor of inosine 5-monophosphate
dehydrogenase, which is required for
de novo synthesis of guanosine nucleotides. Mycophenolate mofetil
inhibits lymphocyte proliferation,
induces apoptosis of activated T-cells,
and inhibits adhesion molecule expression and fibroblast proliferation.
Gastrointestinal toxicity is common
and may respond to dose reduction
or enteric-coated formulation.
Hematologic toxicity is also common, ranging from mild cytopenias
to red cell aplasia. Mycophenolate
mofetil is contraindicated in pregnancy because of case reports suggesting teratogenicity (37).
Indications for Kidney Biopsy in

Patients With SLE*
Increasing serum creatinine without
compelling alternative causes
Confirmed proteinuria 1.0 g/24 h
(either 24-h urine specimens or
spot proteincreatinine ratio)
Combination of the following:
Proteinuria 0.5 1.0 g/24 h +
hematuria (5 red blood
cells/high-power field) or
proteinuria 0.5 1.0 g/24 h +
cellular casts
* From reference 38.
Histopathologic Classification of
Lupus Nephritis
Class I: Minimal mesangial
Class II: Mesangial proliferative
Class III: Focal proliferative
Class IV: Diffuse proliferative (with
active, active and chronic, or
chronic lesions)
Class V: Membranous (with or
without coexisting class III or IV
lupus nephritis)
Class VI: Advanced sclerosing lupus
nephritis with >90% globally
sclerotic glomeruli
In a meta-analysis of 4 selected RCTs evaluating the efficacy of mycophenolate

mofetil vs. cyclophosphamide for induction
therapy, when data on maintenance therapy were excluded mycophenolate mofetil
46. Andrade-Ortega L,
Irazoque-Palazuelos
F, Lpez-Villanueva
R, et al. [Efficacy of
rituximab versus cyclophosphamide in
lupus patients with
severe manifestations. A randomized
and multicenter
study]. Reumatol
Clin. 2010;6:250-5.
[PMID: 21794725]
47. Radhakrishnan J,
Moutzouris DA, Ginzler EM, et al. Mycophenolate mofetil
and intravenous cyclophosphamide are
similar as induction
therapy for class V
lupus nephritis. Kidney Int. 2010;77:15260. [PMID: 19890271]
48. Spetie DN, Tang Y,
Rovin BH, et al. Mycophenolate therapy
of SLE membranous
nephropathy. Kidney
Int. 2004;66:2411-5.
[PMID: 15569333]
ITC4-9
In the Clinic
was not superior to cyclophosphamide in

lupus nephritis (36).
Recently updated guidelines recommend using either cyclophosphamide or mycophenolate mofetil

combined with glucocorticoids for
induction therapy of class III or
IV proliferative lupus nephritis
(38). Response to cyclophosphamide or mycophenolate mofetil
may differ based on race. Asians
and Europeans seem to respond
better to cyclophosphamide than
Hispanics and African Americans
(38).
Maintenance therapy
Current guidelines recommend

either mycophenolate mofetil or azathioprine for maintenance therapy in
lupus nephritis. Both are superior to
cyclophosphamide for this purpose
(39). Evidence from 2 studies of
comparative efficacy of mycophenolate mofetil vs. azathioprine is conflicting (40, 41). Treatment duration
is guided by clinical experience.
In a study of 227 patients with lupus nephritis class III, IV, or V who showed a clinical response to a 24-week induction with either
cyclophosphamide or mycophenolate
mofetil, patients were randomly assigned to
treatment with mycophenolate mofetil
(2 g/d) or azathioprine (2 mg/kg/d). After 3
years of follow up, mycophenolate mofetil
was significantly superior to azathioprine
with respect to time to treatment failure (primary end point), time to renal flare, and
time to rescue therapy (40).
In contrast, an open-label study showed
no significant difference in patients treated
with mycophenolate mofetil vs. azathioprine for maintenance treatment of lupus
nephritis over a period of 4 years. All
patients in the study were initially treated
with low-dose cyclophosphamide for induction therapy (41).
Calcineurin inhibitors, such as cyclosporine, are also used for maintenance therapy.
A multicenter, randomized, open pilot trial
compared the efficacy of cyclosporine vs.
azathioprine for maintenance therapy of
lupus nephritis. Seventy-five patients with
lupus nephritis IV, Vc, or Vd, initially treated

with IV glucocorticoids (1 mg/kg/3 d) followed by oral cyclophosphamide and prednisone for a median of 90 days, were
randomized to treatment with azathioprine
or cyclosporine for 2 (core study) and 4
years. Azathioprine and cyclosporine were
equally effective in preventing disease flares,
the primary outcome of the study. Proteinuria, a secondary end point, decreased significantly with both treatments. Blood
pressure and creatinine clearance did not
change significantly with either treatment;
extrarenal manifestations and clinical activity decreased with both treatments (42).
mofetil for maintenance treatment of

class III or IV lupus nephritis.
Data from this study indicate that

cyclosporine and azathioprine are
equally effective for maintenance
treatment of lupus nephritis and
have similar effects on blood pressure and renal function.
A retrospective analysis of 2 large RCTs

showed similar efficacy of mycophenolate
mofetil and cyclophosphamide for induction therapy of class V lupus nephritis (47).
Tacrolimus, also a calcineurin inhibitor, may be used to treat diffuse

proliferative or membranous lupus
nephritis. Meta-analysis of data
from open-label trials, casecontrol
studies, and RCTs showed that
tacrolimus may be effective as induction and maintenance therapy
for lupus nephritis or in treatment
of refractory lupus nephritis with
persistent proteinuria (43).
Rituximab is a monoclonal antibody
directed against CD20, a membrane
protein expressed on B-cells. Rituximab depletes B-cells from the peripheral blood. Open-label trials
indicated improvement of lupus
nephritis after B-cell depletion; however, RCTs did not show statistically
significant response compared with
placebo (4446).
Current ACR guidelines propose
mycophenolate mofetil or azathioprine as preferred maintenance therapy for proliferative lupus nephritis.
Calcineurin inhibitors or rituximab
combined with glucocorticoids may
be used for patients with an adequate
response to cyclophosphamide or
mycophenolate mofetil (38). To date,
no RCT has directly compared calcineurin inhibitors to mycophenolate
ITC4-10
In the Clinic

therapy for membranous nephritis?
Pure membranous nephritis is not
associated with endocapillary proliferation and presents with variable
degrees of proteinuria. The progression of renal dysfunction is
slow compared with that of class
III or IV lupus nephritis. The evidence to guide treatment of membranous lupus nephritis is limited.
A prospective study of mycophenolate

mofetil combined with renoprotective therapy (with angiotensin inhibitors or angiotensin-receptor blockers) showed that
most patients achieved complete or partial
remission at 6 months and sustained effect
for a mean follow-up of 18 months (48).
Based on this evidence, current

guidelines from the ACR for membranous lupus nephritis recommend
treatment with mycophenolate
mofetil. Tacrolimus and azathioprine have also been studied for induction or maintenance treatment.
A recent open-label trial showed that
tacrolimus or mycophenolate mofetil combined with steroids were both effective in controlling membranous lupus nephritis (49).
An RCT comparing azathioprine with
tacrolimus, both combined with prednisone, for maintenance therapy of membranous nephritis suggests similar low
rates in relapse with both regimens (50).

therapy for neuropsychiatric
lupus?
Treatment of serious neuropsychiatric SLE manifestations is relatively empirical and includes IV
glucocorticoids, immunoglobulin,
and cyclophosphamide.
An RCT comparing cyclophosphamide
with glucocorticoids after 3 days of IV immunoglobulin for treatment of transverse
1 October 2013
myelitis in lupus showed that relapse was

more common in the steroid group (51).
Case reports and small, uncontrolled studies suggest a beneficial

effect of rituximab in treatment of
neuropsychiatric lupus; however,
the relapse rate seems to be high.
therapy for respiratory
manifestations?
Pleuritis responds to treatment with
NSAIDs and low to moderate doses of glucocorticoids. Immunosuppressive treatment is reserved for
refractory cases. Diffuse alveolar
hemorrhage presents abruptly, carries a poor prognosis, and requires
treatment with IV glucocorticoids
and immunosupressants. Plasmapheresis may also be considered.
Pulmonary hypertension is rare in
SLE (0.517%) and may be secondary to vasculopathy, interstitial
pulmonary fibrosis, or in situ
thrombosis (52). SLE patients with
pulmonary hypertension are at high
risk for cardiac failure and early
death. Endothelin-receptor antagonists, phosphodiesterase-5 inhibitors, and prostacyclin analogs
with or without immunosuppressive
medications may be used to treat
pulmonary hypertension in lupus.
An RCT showed efficacy of cyclophosphamide in mild and moderate pulmonary hypertension in patients with SLE
by reducing pulmonary artery systolic
pressure and improving the New York
Heart Association functional class (53).
A retrospective study suggests that patients
with SLE and mild to moderate pulmonary
hypertension may respond to treatment with
cyclophosphamide and glucocorticoids,
while patients with more severe disease may
require combination of vasodilators with immunosuppressants (54).
A small study indicated that interstitial
lung disease treated with glucocorticoids
for at least 1 week resulted in indolent progression or stabilization over time (55).
Larger clinical trials have not been

done, and treatment decisions
are based on clinical experience.
1 October 2013
Azathioprine or cyclophosphamide
is frequently recommended for patients who have not responded to
glucocorticoids (56). Acute lupus
pneumonitis requires treatment
with high doses of glucocorticoids
and cyclophosphamide.
therapy for ocular manifestations?
Depending on the severity of the
ocular involvement and the activity
of the systemic disease, treatment
may include antimalarial agents,
NSAIDs, or oral or IV glucocorticoids. Scleral or retinal involvement
may require concomitant use of
pulse glucocorticoids, followed by
1 mg/kg of prednisone equivalent,
combined with immunosuppressive
therapy (57). Retinal vasculitis and
arterial or venous retinal occlusion
in the presence of antiphospholipid
antibodies may require concomitant
use of immunosuppressive medications and antiplatelet agents or anticoagulation.
Two international, double-blind, phase 3

RCTs compared belimumab 1 mg/kg and
10 mg/kg plus standard therapy to placebo plus standard therapy (58, 59). In the
52-week study, reduction of 4 points on
the SLE Response Index (SRI) was 51% and
58% with the belimumab 1-mg/kg and
10-mg/kg dose, respectively, vs. 44% with
placebo (P<0.05). In the 76-week study, the
SRI-measured response at 52 weeks was
42.8% and 46.5% with the belimumab
1-mg/kg and 10-mg/kg dose and 35.3%
with placebo; at 76 weeks, the response
rates were 42.1% and 41.4% with the belimumab 1-mg/kg and 10-mg/kg dose, and
33.8% with placebo (P<0.05 and P = NS, respectively). Both trials excluded patients
with severe lupus nephritis or severe CNS
manifestations. Analysis of combined results from both trials showed more
improvement of musculoskeletal and mucocutaneous manifestations in patients
treated with belimumab and improvement
49. Yap DY, Yu X, Chen

XM, et al. Pilot 24
month study to
compare mycophenolate mofetil and
tacrolimus in the
treatment of membranous lupus
nephritis with
nephrotic syndrome.
Nephrology (Carlton). 2012;17:352-7.
[PMID: 22295934]
50. Chen W, Liu Q, Chen
W, et al. Outcomes
of maintenance
therapy with
tacrolimus versus
azathioprine for active lupus nephritis:
a multicenter randomized clinical trial.
Lupus. 2012;21:94452. [PMID: 22438027]
51. Kovacs B, Lafferty TL,
Brent LH, et al. Transverse myelopathy in
systemic lupus erythematosus: an
analysis of 14 cases
and review of the literature. Ann Rheum
Dis. 2000;59:120-4.
[PMID: 10666167]
52. Dhala A. Pulmonary
arterial hypertension
in systemic lupus
erythematosus: current status and future direction. Clin
Dev Immunol.
2012;2012:854941.
[PMID: 22489252]
53. Gonzalez-Lopez L,
Cardona-Muoz EG,
Celis A, et al. Therapy
with intermittent
pulse cyclophosphamide for pulmonary hypertension associated with
systemic lupus erythematosus. Lupus.
2004;13:105-12.
[PMID: 14995003]
54. Jais X, Launay D,
Yaici A, et al. Immunosuppressive
therapy in lupusand mixed connective tissue diseaseassociated pulmonary arterial
hypertension: a retrospective analysis
of twenty-three cases. Arthritis Rheum.
2008;58:521-31.
[PMID: 18240255]
55. Weinrib L, Sharma
OP, Quismorio FP Jr.
A long-term study of
interstitial lung disease in systemic lupus erythematosus.
Semin Arthritis
Rheum. 1990;20:4856. [PMID: 2218553]
ITC4-11
What new medications are

available for treating systemic
lupus?
A monoclonal antibody targeting
the B-lymphocyte stimulator
(BLys) was recently approved.
In the Clinic
56. Pego-Reigosa JM,

Medeiros DA, Isenberg DA. Respiratory
manifestations of
systemic lupus erythematosus: old and
new concepts. Best
Pract Res Clin
Rheumatol.
2009;23:469-80.
[PMID: 19591778]
57. Neumann R, Foster
CS. Corticosteroidsparing strategies in
the treatment of
retinal vasculitis in
systemic lupus erythematosus. Retina.
1995;15:201-12.
[PMID: 7569347]
58. Furie R, Petri M, Zamani O, et al; BLISS76 Study Group. A
phase III, randomized, placebo-controlled study of belimumab, a
monoclonal antibody that inhibits B
lymphocyte stimulator, in patients with
systemic lupus erythematosus. Arthritis
Rheum.
2011;63:3918-30.
[PMID: 22127708]
59. Navarra SV, Guzmn
RM, Gallacher AE, et
al; BLISS-52 Study
Group. Efficacy and
safety of belimumab
in patients with active systemic lupus
erythematosus: a
randomised, placebo-controlled, phase
3 trial. Lancet.
2011;377:721-31.
[PMID: 21296403]
60. van Vollenhoven RF,
Petri MA, Cervera R,
et al. Belimumab in
the treatment of systemic lupus erythematosus: high disease activity
predictors of response. Ann Rheum
Dis. 2012;71:1343-9.
[PMID: 22337213]
61. Tseng CE, Buyon JP,
Kim M, et al. The effect of moderatedose corticosteroids
in preventing severe
flares in patients
with serologically active, but clinically
stable, systemic lupus erythematosus:
findings of a
prospective, randomized, doubleblind, placebo-controlled trial. Arthritis
Rheum.
2006;54:3623-32.
[PMID: 17075807]
62. Mok CC, Ho LY, Fong
LS, To CH. Immunogenicity and safety
of a quadrivalent human papillomavirus
vaccine in patients
with systemic lupus
erythematosus: a
case-control study.
Ann Rheum Dis.
2013;72:659-64.
[PMID: 22589375]
in immunologic parameters; in addition,

fewer patients had worsening hematologic
parameters (60).
ITC4-12
The SRI requires reduction in

disease activity scores and no deterioration from baseline in target
organ manifestations (58). Further evidence is needed to assess
the comparative efficacy of BlyS
antagonism in severe lupus manifestations.
How should clinicians monitor
patients who are being treated for
lupus?
Laboratory testing should include
a complete blood count, basic
metabolic panel, and urinalysis on
routine follow-up visits. These
tests allow the clinician to evaluate for hematologic, renal, and
other target-organ manifestations.
Many clinicians also routinely test
for double-stranded DNA antibodies and complement C3 and
C4 levels; however, this practice is
controversial for clinically stable
patients. Although a prospective
RCT showed that 4-week
treatment with prednisone of clinically stable but serologically active patients averts a severe flare
(61), C3 and C4 and doublestranded DNA antibodies are
more useful in assessing SLE activity in symptomatic patients or
in assessing response to treatment.
Other monitoring should be tailored to individual disease manifestations (Table 3). Consideration
should be given to laboratory
monitoring for immunosuppressive medication toxicity and ophthalmologic evaluation of patients
treated with hydroxychloroquine,
particularly those older than
40 years who have been treated for
a long period. Clinicians should be
alert to osteoporosis prevention
and prescribe treatment when appropriate. Clinicians should also
consider periodic lipid testing and
order lipid-lowering agents, as
needed.
In the Clinic
What should clinicians do about

immunizations in people with
lupus?
All patients with SLE should receive influenza and pneumococcal
vaccinations. In addition, a recent
study showed that the quadrivalent
human papillomavirus vaccine is
well-tolerated and reasonably effective in patients with stable SLE
and does not induce an increase in
lupus activity or flares (62). Patients receiving immunosuppressive therapy or daily prednisone
>20 mg should not receive live attenuated vaccines, including herpes zoster (shingles), Flumist,
measles-mumps-rubella, and
smallpox. Tuberculin skin testing
is recommended for SLE patients
requiring prolonged treatment
with glucocorticoids or immunosuppressive therapy.
How should clinicians modify
treatment for pregnant patients?
Fertility is not significantly affected in SLE; however, flares
occur at a higher rate during
pregnancy and the immediate
postpartum period. The presence
of anti-SSA antibodies may predict adverse pregnancy outcomes,
as may other factors, including
antiphopsholipid antibodies, renal
disease, thrombocytopenia, hypertension, and use of prednisone.
Becoming pregnant during clinical remission correlates with less
frequent and severe lupus exacerbations. The initial presentation
of SLE with hematologic or renal
manifestations during pregnancy
is not uncommon. Clinicians
should also consider pregnancyrelated hematologic, vascular, and
renal abnormalities that mimic
SLE manifestations, including
eclampsia and the HELLP syndrome (a group of symptoms that
occurs in pregnant women with
hemolysis, elevated liver enzymes,
and low platelet counts). Antimalarials can be used safely in
pregnant SLE patients (63).
Active lupus manifestations in
1 October 2013
pregnancy are usually treated with

hydroxychloroquine and prednisone. It is advisable to continue
hydroxychloroquine in pregnancy
because discontinuation is associated with increased risk for flares
and pregnancy is associated with
risk for increased disease activity.
Hydroxychloroquine may also
protect against cardiac manifestations of neonatal lupus.
For severe manifestions, IV glucocorticoids and azathioprine may be
considered because azathioprine
has not been identified as a human
teratogen (64). Mycophenolate
mofetil, cyclophosphamide, and
methotrexate are contraindicated
due to potential teratogenicity.
When should patients with lupus
be hospitalized?
Patients with serious complications should be hospitalized.
Indications include severe thrombocytopenia, severe or rapidly progressive renal disease, suspected
lupus pneumonitis or pulmonary
hemorrhage, and severe cardiovascular or CNS manifestations. A
major cause of death in SLE is infection, including from opportunistic pathogens. SLE patients
with unexplained fever should be
hospitalized for evaluation and
initiation of treatment with antibiotics. Empirical coverage should
include Staphyloccocus aureus,
Pseudomonas species, Klebsiella
species, Escherichia coli, and Acinetobacter species. Chest pain in lupus
patients could be due to coronary
artery disease, serositis, pulmonary
embolism, or esophageal disease.
Lupus increases the risk for endothelial dysfunction, and long-term
treatment with steroids increases
traditional risk factors for coronary
artery disease (65). Neurologic
symptoms in lupus patients may
be due to neuropsychiatric lupus,
infection, the antiphospholipid
syndrome, or hypertension. All lupus patients with acute neurologic
manifestations should be admitted
1 October 2013
Table 3. Recommended Follow-up of Patients With SLE

Issue
How
Frequency
Disease activity
History (rash, joint pain

constitutional symptoms);
physical examination;
CBC, urinalysis, CMP
Quarterly
Nephropathy
CMP, urinalysis, urine protein Quarterly, if inactive disease,

creatinine ratio
or monthly, to assess response
to treatment
Hyperlipidemia
Fasting lipid profile
Yearly
Hydroxychloroquine toxicity
History (visual disturbances);

ophthalmologic evaluation
Yearly
MMF, AZA toxicity
CBC, CMP
Every 812 wk or 4 wk after

change in dose
Cervical dysplasia on
immunosuppressants
Gynecologic examination;
PAP smear, HPV test
Yearly
Osteonecrosis
History, x-rays or MRI of

affected joint
With symptoms and history

suggestive of avascular necrosis
Thrombosis
History, examination venous

duplex studies, imaging for
pulmonary embolism
With symptoms or signs

suggestive of thrombosis
Pulmonary hypertension
Echocardiography
Yearly, or as clinically indicated
Osteoporosis
DEXA
Every 12 years, while on

steroids
Planned pregnancy
Antiphospholipid antibodies
urinalysis, anti-SSA/SSB
antibodies, CBC, CMP, and
complement C3 and C4
Before conception
Patient education
Every visit
AZA = azathioprine; CBC = complete blood count; CMP = comprehensive metabolic panel;
DEXA = dual x-ray absorptiometry; HPV= human papillomavirus; MMF = mycophenolate mofetil;
MRI = magnetic resonance imaging; PAP = Papanicolaou.
and rapidly evaluated with appropriate imaging, cerebrovascular

fluid analysis, echocardiogram, and
laboratory studies.
What nondrug therapies should

clinicians recommend?
All lupus patients should be
counseled on low-cholesterol diet,
63. CostedoatChalumeau N,
Amoura Z, Duhaut P,
et al. Safety of hydroxychloroquine in
pregnant patients
with connective tissue diseases: a study
of one hundred thirty-three cases compared with a control
group. Arthritis
Rheum.
2003;48:3207-11.
[PMID: 14613284]
64. Natekar A, Pupco A,
Bozzo P, Koren G.
Safety of azathioprine use during
pregnancy. Can Fam
Physician.
2011;57:1401-2.
[PMID: 22170192]
ITC4-13
When should clinicians consider

consulting a rheumatologist or
other specialist?
A rheumatologist should be involved in the treatment of all lupus
patients (66). Other specialists also
may be involved, according to organ-specific disease manifestations.
In the Clinic
In the Clinic
Tool Kit
Systemic Lupus
Erythematosus
such as osteoporosis or the Sjogren

syndrome, is also recommended. All
patients should be counseled on the
daily requirements for calcium and
vitamin D to prevent osteoporosis.
Routine dental evaluation is also
recommended.
Treatment... Hydroxychloroquine prevents disease flares and is considered the

cornerstone of SLE treatment. Glucocorticoids are first-line agents for most SLE
manifestations, with dosage and treatment duration based on clinical experience
and consensus. Immunosuppressive treatment in lupus nephritis is based on
histopathologic classification and guided by ACR recommendations. Treatment of
other lupus manifestations is based on sparse evidence from clinical trials and
clinical experience and often requires immunosuppressive therapy and a multidisciplinary approach.
PIER Module
http://smartmedicine.acponline.org/content.aspx?gbosId=153
Smart Medicine module on systemic lupus erythematosus (SLE)
from the American College of Physicians.
Patient Information
www.nlm.nih.gov/medlineplus/lupus.html
www.nlm.nih.gov/medlineplus/tutorials/lupus/htm/index.htm
www.nlm.nih.gov/medlineplus/spanish/tutorials/lupusspanish/
htm/index.htm
Resources related to lupus from the National Institutes of Healths
MedlinePLUS, including an interactive tutorial in English and
Spanish.
www.niams.nih.gov/Health_Info/Lupus/lupus_ff.asp
www.niams.nih.gov/Portal_En_Espanol/Informacion_de_Salud/Lupus/
default.asp
Answers to common questions about lupus from the National Institute
of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), in
English and Spanish.
www.nlm.nih.gov/medlineplus/ency/article/000481.htm
Information about lupus nephritis, a complication of SLE from
NIAMS.
Clinical Guidelines
www.rheumatology.org/Practice/Clinical/Guidelines/Glucocorticoid
-Induced_Osteoporosis_(Members__Only)/
Recommendations for the prevention and treatment of glucocorticoidinduced osteoporosis from the American College of Rheumatology
(ACR) in 2010.
Diagnostic Tests and Criteria

pier.acponline.org/physicians/diseases/d208/tables/d208
-tlab.html
List of laboratory and other studies for SLE from PIER.
www.rheumatology.org/practice/clinical/position/ana_position
_stmt.pdf
Position statement on the methodology of testing for antinuclear
antibodies from the ACR in 2011.
ITC4-14
In the Clinic
In the Clinic
65. Petri M, Lakatta C,

Magder L, et al. Effect of prednisone
and hydroxychloroquine on coronary
artery disease risk
factors in systemic
lupus erythematosus: a longitudinal
data analysis. Am J
Med. 1994;96:254-9.
[PMID: 8154514]
66. Gabriel S, Tugwell P,
OBrien B, et al. Report of the OMERACT task force on
economic evaluation. Outcome
Measures in
Rheumatology. J
Rheumatol.
1999;26:203-6.
[PMID: 9918264]
exercise, weight control, and smoking cessation. They should also be

advised about protection from ultraviolet rays to reduce flares from sun
exposure. Prevention or treatment of
complications due to conditions
commonly associated with lupus,
1 October 2013
THINGS YOU SHOULD

KNOW ABOUT LUPUS
In the Clinic
What is lupus?
A chronic disease that occurs when the bodys defense system (the immune system) wrongly attacks
its own tissues.
The result can be pain and swelling (inflammation)
that affects the skin, joints, kidneys, and other
organs.
Symptoms range from mild to serious and fluctuate
between times when the disease is active (a flare)
and times when it is quiet (remission).
The cause is unclear.
Lupus usually starts when people are in their 20s
and 30s and is 10 times more common in women
than in men.
What are the signs and symptoms?
How is it diagnosed?
Your doctor will examine you carefully and ask you
about your symptoms.
Your doctor may order blood tests that can help
confirm whether you have the disease.
How is it treated?
Nonsteroidal anti-inflammatory drugs to decrease
swelling, pain, and fever.
Antimalarial drugs (such as hydroxychloroquine) to

reduce fatigue, rashes, joint pain, and mouth sores.
Corticosteroids or biologics, a new type of drug for
rheumatic diseases, to reduce inflammation.
Treatment is based on the symptoms and the severity
of the disease.
For More Information

www.niams.nih.gov/Health_Info/Lupus/default.asp
Booklet on SLE to help people understand the disease and how

to cope with it, from the NIAMS.
www.rheumatology.org/Practice/Clinical/Patients/Diseases_And
_Conditions/Systemic_Lupus_Erythematosus_(Lupus)/
www.rheumatology.org/Practice/Clinical/Patients/Diseases_And
_Conditions/Lupus_Eritematoso_Sistemico_(Lupus)_(Espaol)/
Information about SLE from the ACR, in English and Spanish.
Patient Information
Fatigue.
Rashes (particularly a butterfly-shaped rash over the
cheeks or a red rash with raised round or oval
patches).
Painful and swollen joints.
Sores in the mouth or nose.
Chest pain when breathing deeply, from swelling of
the tissue lining the lungs (pleurisy or pleuritis) or
the heart (pericarditis).
Mental health problems, seizures, or strokes.
Fever.
Kidney problems, liver disease, clogged arteries
(atherosclerosis).
CME Questions
1. A 25-year-old woman is evaluated for a

1-year history of scaly plaques on her
face and scalp. Results of a skin biopsy
1 week ago are consistent with chronic
cutaneous lupus. She has ongoing mild
fatigue, a 10-day history of lower back
pain, and occasional migraine headaches
for which she takes sumatriptan as
needed. She also has a history of partialonset seizures that began at age 13 years
for which she currently takes phenytoin.
On physical examination, temperature is
37.0C (98.6F), blood pressure is
125/73 mm Hg, pulse rate is 72/min, and
respiration rate is 16/min. Cutaneous
examination reveals scattered circular
plaques on the cheeks, nose, scalp, and
ear canals. Within the plaques, there is
follicular plugging and atrophic scarring.
She also has patches of alopecia where
the rash is present on the scalp.
Cardiopulmonary examination is normal.
There is no lymphadenopathy or oral
ulcers. Abdominal examination is
unremarkable. Musculoskeletal
examination reveals no synovitis, and
neurologic examination is normal.
Laboratory studies reveal the following:
hemoglobin, 14 g/dL (140 g/L); leukocyte
count, 6300/L (6.3 109/L); erythrocyte
sedimentation rate, 16 mm/h; serum
creatinine, 0.8 mg/dL (61.0 mol/L);
serum complement (C3 and C4), normal;
antinuclear antibodies, titer of 1:160;
antidouble-stranded DNA antibodies,
negative; anti-Ro/SSA antibodies,
negative; anti-La/SSB antibodies,
negative; anti-Smith antibodies,
negative; antiribonucleoprotein
antibodies, negative; antihistone
antibodies, negative; urinalysis, normal.
Which of the following is the most likely
diagnosis?
A. Discoid lupus
B. Drug-induced lupus
C. Mixed connective tissue disease
D. Systemic lupus erythematosus
2. A 28-year-old woman with systemic

lupus erythematosus (SLE) is evaluated in
the office after obtaining positive results
on a home pregnancy test. She has a
1-month history of nausea but is
otherwise asymptomatic. Her last
menstrual period was 2 months ago. This
is her first pregnancy. Her SLE is wellcontrolled with hydroxychloroquine, and
her last flare was 10 months ago.
On physical examination, temperature is
36.2C (97.2F), blood pressure is
110/72 mm Hg, pulse rate is 76/min,
and respiration rate is 16/min. Physical
examination is normal. A repeated
pregnancy test is positive.
Laboratory studies reveal the following:
hemoglobin, 12.1 g/dL (121 g/L);
leukocyte count, 5400/L (5.4 109/L);
platelet count, 342 000/L (342 109/L);
serum creatinine, 0.7 mg/dL (53.4 mol/L);
serum complement (C3 and C4), normal;
antinuclear antibodies, titer of 1:2560;
anti-Ro/SSA antibodies, positive;
antidouble-stranded DNA antibodies ,
negative; anti-Smith antibodies,
positive;urinalysis, normal.
She seeks advice on how to manage her
SLE during her pregnancy.
Which of the following is the most
appropriate management of this patient?
A. Discontinue hydroxychloroquine
B. Recommend termination of pregnancy
C. Start prednisone
D. No change in management
3. A 43-year-old woman with SLE is
admitted to the hospital for a 1-week
history of worsening headache and a
2-day history of confusion, personality
change, and emotional lability. She was
diagnosed with lupus 1 year ago, and her
condition has been well-controlled with
prednisone, hydroxychloroquine, and
ibuprofen. Four months ago, prednisone
was discontinued.
occasional headache. Two weeks ago, she

was evaluated in the office for a
1-month history of purpuric lesions on
her legs, palms, and soles. Biopsy
specimen of a lesion showed
leukocytoclastic vasculitis. At that time,
prednisone, 40 mg/d, was initiated, and
the purpuric lesions began to fade.
On physical examination today,
temperature is 37.9C (100.2F), blood
pressure is 150/80 mm Hg, pulse rate is
102/min, and respiration rate is 20/min.
The purpuric lesions persist. She is
confused and oriented to name only,
intermittently laughs and cries, and has
paranoid ideation. She does not have
photophobia or nuchal rigidity, and the
neurologic examination is nonfocal.
Laboratory studies show the following:
hemoglobin, 11.1 g/dL (111 g/L); leukocyte count, 3500/L (3.5 109/L); platelet count, 200 000/L (200 109/L);
erythrocyte sedimentation rate, 83 mm/h;
serum complement (C3 and C4), decreased; ANA, titer of 1:2560. Cerebrospinal fluid findings are as follows:
leukocyte count, 55/L (100% lymphocytes); erythrocyte count, 1/L; protein,
72 mg/dL (720 mg/L); gram stain,
negative; venereal disease, negative.
Culture results are pending. T2-weighted
magnetic resonance imaging of the brain
reveals scattered punctate areas of
increased signal in the periventricular
and subcortical white matter.
Which of the following is the most
appropriate next step in this patients
treatment?
A. Begin ampicillin and gentamicin
B. Begin methylprednisolone and
cyclophosphamide
C. Discontinue ibuprofen
D. Schedule plasmapheresis
Two months ago, she developed fatigue,

intermittent low-grade fevers, and
Questions are largely from the ACPs Medical Knowledge Self-Assessment Program (MKSAP, accessed at
http://www.acponline.org/products_services/mksap/15/?pr31). Go to www.annals.org/intheclinic/
to complete the quiz and earn up to 1.5 CME credits, or to purchase the complete MKSAP program.
ITC4-16
In the Clinic
1 October 2013

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Systemic Lupus

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ystemic lupus erythematosus (SLE, lupus) is a condition in which the

2013 American College of Physicians

Which patients are at elevated

dysfunction in genetically predisposed individuals.

Annals of Internal Medicine

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Should clinicians screen

CLINICAL BOTTOM LINE

What other clinical manifestations

11. Vil LM, Alarcn GS,

2013 American College of Physicians

Annals of Internal Medicine

The malar rash may be confused

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18. Hochberg MC. Updating the American

2013 American College of Physicians

Hispanics (61%) and African

Cytopenias are common in patients

Renal involvement is a common

affecting 3050% of patients (16).

Neuropsychiatric SLE manifestations may be caused by vasculopathy,

Ocular manifestations include keratoconjuctivitis sicca (with or without

Involvement of the respiratory system may be primary or secondary.

Gastrointestinal symptoms may

Annals of Internal Medicine

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diagnosing SLE, based on objective

Table 1. American College of Rheumatology Classification Criteria for SLE*

Erythematous raised patches or atrophic scarring (older lesions)

Skin rash as a result of unusual reaction to sunlight

Usually painless oral or nasopharyngeal ulcerations, observed by physician

Nonerosive arthritis, involving 2 or more peripheral joints characterized by tenderness and

Pleuritis: Convincing history of pleuritic pain or rubbing heard by physician, or evidence of

Persistent proteinuria >0.5 g/d or >3 on dipstick

Seizures (in the absence of offending drugs or metabolic derangement)

Hemolytic anemia: with reticulocytosis

Detected by immunofluoresence (or equivalent assay) in the absence of drugs known to be

*From reference 18.

Annals of Internal Medicine

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26. Badsha H, Kong KO,

2013 American College of Physicians

Basic Investigations for SLE

33. Illei GG, Austin HA,

RNP, which are collectively referred

extractable nuclear antigens, are rare

CLINICAL BOTTOM LINE

2013 American College of Physicians

What medications are used to

glucocorticoids, antimalarial agents,

Annals of Internal Medicine

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Table 2. Drug Treatment for SLE

Low: 7 mg/d; medium:

Fluid retention, diabetes mellitus,

200400 mg/d (orally)

Skin hyperpigmentation, retinal toxicity

Inhibits lymphocyte proliferation