Asthma Pathophysiology: Ixsy Ramirez, MD, MPH Pediatric Pulmonology University of Michigan, C.S. Mott Children's Hospital

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Asthma

Pathophysiology
Ixsy Ramirez, MD, MPH
Pediatric Pulmonology
University of Michigan, C.S. Mott Children’s Hospital
Definition of Asthma
 Chronic inflammatory disorder of the airways
 Mast cells, eosinophils, T lymphocytes, macrophages,
neutrophils, epithelial cells
 Causes variable and recurrent episodes of
wheezing, breathlessness, chest tightness,
cough – especially at night or early morning
 Associated with widespread, but variable airflow
obstruction that is often reversible

NHLBI Asthma Guidelines, EPR-3, Aug 2007


NHLBI Asthma Guidelines, EPR-3, Aug 2007
Asthma Pathophysiology
Individual Inflammation Impact

Genetic predisposition Inflammation underlies disease Clinical symptoms also vary by


Intrinsic vulnerability processes individual and over time
Gene-environment Phenotype varies by individual
interact: and over time
Atopy / allergy
Infection
Airflow Limitation
 Induced by airway inflammation
 Bronchoconstriction- Bronchial smooth muscle contraction
that quickly narrows the airways in response to exposure to a
variety of stimuli
 Airway hyperresponsiveness- an exaggerated
bronchoconstrictor response to stimuli
 Airway edema- as the disease becomes more persistent and
inflammation become more progressive, edema, mucus hyper
secretion, and formation of inspissated mucus plugs further
limit airflow.

NHLBI Asthma Guidelines, EPR-3, Aug 2007


Pathophysiology
Pathology
Remodeling
 Reversibility of airflow limitation may be incomplete in
some patients.
 Persistent changes in airway structure
 Sub-basement fibrosis
 Mucus hypersecretion
 Injury to epithelial cells
 Smooth muscle hypertrophy
 Angiogenesis
Histopathology of asthma
Normal Asthma

Same in both pictures (x 300)

• Tight structure with a predominance of • Less ciliated cells


ciliated epithelial cells. • Goblet cells hyperplasia
• Only few goblet cells in the epithelium. • Epithelium and lamina propia are
• The lamina propia, is practically cell- highly infiltrated (mainly eosinophils and
free. lymphocytes)
• Inflammatory cells are not seen. • Edema
• Basement membrane thickening
Laitinen et.al. Allergy Proc 15,6:323, 1994 • Collagen deposition in the sub mucosa
Consequences of Remodeling in
Asthma
Smooth Mucous Inflammatory Fibrogenic Elastolysis
muscle mass glands cells growth factor
increase increase persistence release
Reduced
elasticity of
airway wall
Important mucus
Collagen
secretion during
deposition on
exacerbation
RBM and ECM
Severe Ongoing
bronchospasm inflammation
during
exacerbation

Bousquet J, et al. Am J Respir Crit Care Med. 2000;161(5):1720-1745.


Histopathology of Status Asthmaticus
In fatal exacerbations the pathology is dominated
by extensive plugging of the conducting airways
with mucus and extracellular debris
Changes in the Asthmatic Airway

Inflammation

Smooth Muscle
Changes

Flow Expiration Flow Expiration

Volume Volume

Inspiration Inspiration
FEV1/FVC < 75-80% = Obstruction
Causes of Asthma
 Interplay between host factors (primarily genetics),
and environmental exposures that occur at a
crucial time in the development of the immune
system.
 A definitive cause is unknown.
Causes of Asthma

NHLBI Asthma Guidelines, EPR-3, 2007


Clinical Heterogeneity of Asthma
 Allergic versus nonallergic asthma
 Late- versus early- onset asthma
 Exercise-induced asthma
 Nocturnal asthma
 Asthma with prominent symptom of cough
Pathogenesis of Asthma

NHLBI Asthma Guidelines, EPR-3, 2007


Asthma Pathophysiology –Therapeutic
Implications

Short and Inhaled


Long-Acting Smooth Muscle Airway Corticosteroids
Dysfunction Inflammation
Beta2-Agonists Leukotriene
Antagonists

• Bronchoconstriction • Inflammatory cell


 • Bronchial hyperreactivity

infiltration/activation
 • Hypertrophy/Hyperplasia
 • Mucosal edema 
• Inflammatory mediator
 release
• Cellular proliferation 
• Epithelial damage 
• Basement membrane 
thickening

Symptoms/Exacerbation
s

Adapted from Bousquet et al. Am J Respir Crit Care Med. 2000;161:1720-1745.


Environmental Factors
 Allergens
 House dust mite
 Alternaria
 Cockroach/mouse
 Pets
 Infections
 Atopic interaction
 RSV, parainfluenza – young
 Rhinovirus
 Others
 Tobacco smoke
 Pollution/Occupation
 Obesity?
Natural History of Asthma - Children
 Majority of persistent asthma symptoms begin
before age 3
 Younger onset (< 3yo vs >6 yo) is associated
with lower FEV1 at 11-16 yrs (Morgan 2005,
CAMP 2000)
 Majority of asthmatics < 3yo will not wheeze at
> 6yo
Asthma in Adults
 Evidence for lower overall lung function in adults
with asthma (James, 2005)
 Variable information about rate of decline, when
other factors (smoking, COPD) excluded (Sherrill
2003, Griffith 2001)
Questions?

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