Preventing Cardiovascular Disease in Patients With.2 PDF
Preventing Cardiovascular Disease in Patients With.2 PDF
Preventing Cardiovascular Disease in Patients With.2 PDF
Vol. 31, No. 3, pp 198Y200 x Copyright B 2016 Wolters Kluwer Health, Inc. All rights reserved.
Progress in Prevention
198
easily achieve lower BP levels with- poprotein cholesterol (HDL-C) are risk in those on combination ther-
out undue treatment burden.2 the most prevalent pattern of dys- apy.7 Combination therapy with
Patients with DM2 have an in- lipidemia in persons with DM2. niacin is therefore not recommended.
creased prevalence of lipid abnor- The evidence base for medications The ADA standards suggest that the
malities, contributing to their high that target these lipid particles is use of niacin and fibric acid deriva-
risk of CVD. Subgroup analysis of much less robust than that for statin tives may be limited to patients with
diabetic patients within large clin- therapy. The ADA standards recom- hypertriglyceridemia and low HDL-C
ical trials and trials in patients with mend dietary and lifestyle modifica- levels who are intolerant of statins.2
diabetes showed significant reduc- tions as first line of management of Lifestyle intervention including
tions in incident and recurrent hypertriglyceridemia, unless the dietary changes, increased physical
cardiovascular events and CVD- triglyceride level is greater than activity, weight loss, and smoking
related mortality. Meta-analyses 1000 mg/dL, in which case imme- cessation, together with medica-
including data from over 18 000 diate pharmacologic therapy with tion management, is helpful in
patients with diabetes from 14 ran- omega-3 fatty acids or fibric acid managing many CVD risk factors,
domized trials of statin therapy derivatives may reduce the risk of including hypertension and dyslip-
demonstrate a 9% proportional re- acute pancreatitis.2 In a large clini- idemia. Nutrition intervention
duction in all-cause mortality and cal trial specific to diabetic patients, should be individualized with a gen-
13% reduction in vascular mortal- fenofibrate showed no benefit for eral focus on reducing saturated fat,
ity for each mmol/L reduction in CVD risk reduction. In the AC- cholesterol, and trans-fat intake
low-density lipoprotein cholesterol CORD study, combination therapy while increasing omega-3 fatty
(LDL-C). Statins are the drug of with simvastatin and fenofibrate acids and viscous fiber. Glycemic
choice for LDL-C lowering and showed no added CVD risk reduc- control can also help to improve
cardio-protection.2 tion benefit when compared with plasma lipid levels, particularly in
Most trials of statins and CVD simvastatin alone.6 patients with very high triglyceride
outcomes tested specific doses of The Atherothrombosis Interven- levels and poor glycemic control.2
statins against placebo or other tion in Metabolic Syndrome With Lifestyle interventions targeting
statins rather than aiming for spe- Low HDL/High Triglycerides: Im- weight loss through decreased ca-
cific LDL-C targets. With consid- pact on Global Health Outcomes loric intake and increased physical
eration of the conduct and trial evaluated the benefit of statin activity as implemented in the Ac-
outcomes of these trials, the 2015 plus extended-release niacin in pa- tion for Health in Diabetes (Look
ADA Standards of Care were re- tients with established CVD, low AHEAD) trial may be considered
vised to recommend when to initi- LDL-C and HDL-C levels, and high for improving glucose control, fit-
ate and intensify statin therapy triglyceride levels; about a third of ness, and some CVD risk factors.
based on a patients risk level the study population were also However, the trial was stopped early
(Table 1).2 The standards recom- diabetic. The trial was halted early on the basis of a futility analysis that
mend screening lipid panels at the because of lack of efficacy in rela- demonstrated no reduction in the
time of diagnosis of diabetes and tion to the primary CVD outcome rate of CVD events in overweight
at least annually thereafter mainly (death from coronary heart disease, or obese adults with DM2 as a res-
to evaluate for adherence to med- nonfatal MI, ischemic stroke, hos- ult of intensive lifestyle intervention.8
ication therapy. pitalization for acute coronary syn- One explanation of these findings
Hypertriglyceridemia and low drome, or revascularization) and a is that those with improved CVD
cardio-protective high-density li- possible increase in ischemic stroke risk factor profiles stopped taking
known cardioprotective therapies
TABLE 1 such as statins for dyslipidemia.3
Recommendations for Statin Therapy in Adults With
Thus, it is reassuring to know that
Diabetes (Type 2 Diabetes Mellitus)
there was no increase in CVD events
Age Risk Factor Profile Statin Dose in those who were able to control
G40 y None None risk factors with accepted lifestyle
CVD risk factor(s) Moderate or high changes.
Known CVD High
Antiplatelet therapy with aspi-
40Y75 y None Moderate
CVD risk factors High rin has been shown to be effective
Overt CVD High in reducing CVD morbidity and
975 y None Moderate mortality in high-risk patients with
CVD risk factors Moderate or high previous MI or stroke (secondary
Overt CVD High
prevention). It is less clear whether
Abbreviation: CVD, cardiovascular disease. aspirin is helpful in people without
CVD, including those with diabetes prevalence of diabetes increased in 4. ACCORD Study Group; Cushman
(primary prevention). Two random- the overall population and in all WC, Evans GW, et al. Effects of in-
tensive blood-pressure control in type
ized controlled trials that specifi- subgroups evaluated.10 Given these 2 diabetes mellitus. N Engl J Med.
cally looked at aspirin use in adults growing numbers and the strong 2010;362:1575Y1585.
with diabetes, failed to show a sig- association between diabetes and 5. Patel A; ADVANCE Collaborative
nificant reduction in CVD end CVD risk, it is imperative that we Group; MacMahon S, et al. Effects
adopt an all hands on deck men- of a fixed combination of perindopril
points. The Antithrombotic Trialists
and indapamide on macrovascular
collaborators published a meta- tality when it comes to management and microvascular outcomes in pa-
analysis of 6 large trials of aspirin of diabetes and its coexisting meta- tients with type 2 diabetes mellitus
for primary prevention in the gen- bolic CVD risk factors. Nurse-led (the ADVANCE trial): a randomised
eral population. Of the 95 000 par- diabetes self-management programs controlled trial. Lancet. 2007;370:
have demonstrated benefit with re- 829Y840.
ticipants included in this analysis, 6. ACCORD Study Group; Ginsberg HN,
approximately 4000 were diabetic. gard to improved glycemic control Elam MB, et al. Effects of combina-
The effects of aspirin on major vas- and reduction in CVD risk factors.11 tion lipid therapy in type 2 diabetes
cular events (MI and stroke) were These programs should be used mellitus. N Engl J Med. 2010;362:
similar for patients with or without and expanded to meet the growing 1563Y1574.
demand. Healthcare providers in 7. AIM-HIGH Investigators; Boden
diabetes: relative risk of 0.88 (95% WE, Probstfield JL, et al. Niacin in pa-
confidence interval, 0.67Y1.15) all community, primary and cardio- tients with low HDL cholesterol levels
and 0.87 (95% confidence interval, vascular care settings must be em- receiving intensive statin therapy.
0.79Y0.96), respectively.9 Aspirin powered to screen and treat CVD N Engl J Med. 2011;365:2255Y2267.
seems to have a modest effect on risk factors in people with diabetes 8. Look AHEAD Research Group;
with current, evidenced-based life- Wadden TA, West DS, et al. The Look
CVD event reduction, with the AHEAD study: a description of the
greatest benefit for those with the style and pharmacologic interventions lifestyle intervention and the evi-
highest CVD risk. The benefit of to reduce risk and prevent disease. dence supporting it. Obesity (Silver
aspirin use must be evaluated in Spring). 2006;14:737Y752.
9. Antithrombotic Trialists (ATT) Col-
context with the risk of gastroin-
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(75Y162 mg/d) may be considered and secondary prevention of vascular
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of CVD events 910%). This includes diovascular disease and risk manage- 10. Menke A, Casagrande S, Geiss L,
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evidence: a scientific statement from management education on glycosylated
prevalence of diabetes was 12% to the American Heart Association and hemoglobin and cardiovascular risk
14% among US adults. Between the American Diabetes Association. factors: a meta-analysis. Diabetes Educ.
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