Alpha 1-antitrypsin deficiency
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Alpha 1-antitrypsin deficiency
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Preguntas del estilo USMLE Step 1
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The physician suspects a genetic condition. Which of the following is most likely to reveal the cause of this patient’s underlying disease process?
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Alpha-1 antitrypsin deficiency is a genetic disorder in which a protein called alpha-1 antitrypsin is defective or absent, and it causes lung and liver disease.
Trypsins are a type of protease, which is an enzyme that can break down other proteins.
So this antitrypsin protein is a protease inhibitor, and inactivates trypsins, thereby preventing protein breakdown.
The “alpha-1” is just a holdover from when the protein was discovered – a letter and number combination given before its role was known.
Now, in the lungs, if we zoom in on a tiny alveolus—where gas exchange happens—if there’s some sort of infection or other cause of inflammation, immune cells like neutrophils arrive on the scene.
Neutrophils make an enzyme called neutrophil elastase, a protease capable of breaking down elastin, which is an extracellular matrix protein that gives elasticity and strength to lung tissues.
So while these little guys can help fight off infection by breaking down proteins of the bacteria, it can also go on to break down that precious elastin.
Fortunately, the liver makes alpha-1 antitrypsin which gets released into the blood and sent to the lungs, where it inhibits neutrophil elastase just like it inhibits trypsin, inactivating it before it can break down the protein elastin.
Without alpha-1 antitrypsin, the opposite happens - neutrophil elastase goes unchecked, and it damages the walls of the alveoli, and without that elastin, the alveoli loses its elasticity and structural integrity.
Zooming out a bit and looking at the acinus, which is a bunch of alveoli, it just turns into one big cavity. This destruction and enlargement of the air spaces is called emphysema.
It turns out that emphysema can develop in a couple different ways, and alpha-1 antitrypsin deficiency causes pan-acinar emphysema, meaning the whole acinus is affected, and it also tends to affect the lungs’ lower lobes the most.
Another effect of unchecked inflammation in alpha-1 antitrypsin deficiency is chronic bronchitis, resulting from increased mucus production and narrowing of the airways.
So alpha-1 antitrypsin deficiency can lead to both emphysema and chronic bronchitis, the two types of chronic obstructive pulmonary disease, or COPD.
Another, more common cause of COPD is smoking, and if someone with alpha-1 antitrypsin deficiency also smokes, they tend to get an earlier onset of COPD than they have otherwise, an example of a gene-environment interaction.
Fuentes
- "Robbins Basic Pathology" Elsevier (2017)
- "Harrison's Principles of Internal Medicine, Twentieth Edition (Vol.1 & Vol.2)" McGraw-Hill Education / Medical (2018)
- "Pathophysiology of Disease: An Introduction to Clinical Medicine 8E" McGraw-Hill Education / Medical (2018)
- "CURRENT Medical Diagnosis and Treatment 2020" McGraw-Hill Education / Medical (2019)
- "Alpha-1-Antitrypsin Deficiency Liver Disease" Clinics in Liver Disease (2018)
- "The Diagnosis and Management of Alpha-1 Antitrypsin Deficiency in the Adult" Chronic Obstructive Pulmonary Diseases: Journal of the COPD Foundation (2016)