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Alpha-1-Antitrypsin Deficiency
Aka: Alpha-1-Antitrypsin Deficiency
- See Also
- COPD
- Emphysema
- Chronic Bronchitis
- COPD Management
- Acute Exacerbation of Chronic Bronchitis
- Antibiotic Use in COPD Exacerbation
- COPD Exacerbation Prevention
- COPD Action Plan
- Epidemiology
- Age of onset: 20 to 50 years
- Pathophysiology
- Serpina1 gene defect (Chromosome 14q31-32.3) results in Alpha-1 antitrypsin deficiency
- Alpha-1 antitrypsin protects against the Leukocyte enzyme Neutrophil elastase
- When Alpha-1 antitrypsin is deficient, neutophil elastase results in tissue damage
- Lung alveolar damage (most common)
- Liver injury (less common)
- Skin Injury (rare)
- Presentations: Clinical manifestations that warrant screening
- Emphysema onset before age 45 years
- Emphysema without Tobacco exposure or occupational exposure
- Emphysema predominantly affecting the lower lung lobes
- Idiopathic Chronic Hepatitis
- Family History of COPD or Bronchiectasis at a young age or without risk factors
- Labs
- Serum alpha-1 antitrypsin
- Deficiency: Level <1.5 g/L (<20 umol/L)
- Management
- See COPD Management
- Eliminate exacerbating exposures
- Avoid Tobacco exposure
- Avoid occupational exposures of airborne toxins
- Substitution therapy with human alpha-1 antitrypsin
- Weekly injection of alpha-1-antitrypsin (60 mg/kg) from pooled human plasma
- Indicated in non-smokers, progressive COPD, and serum level <0.8 g/L (<11 umol/L)
- Complications
- Chronic Obstructive Pulmonary Disease (Emphysema)
- Neonatal Hepatitis
- Chronic Hepatitis (adults)
- Cirrhosis (and associated risk of Hepatocellular Carcinoma)
- Granulomatosis with Polyangiitis (previously known as Wegener's Granulomatosis, rare)
- Skin Necrotizing Panniculitis (rare)
- References
- Kohnlein (2008) Am J Med 121:3-9 [PubMed]