- Alpha 1-antitrypsin deficiency
Name = Alpha 1-antitrypsin deficiency
ICD10 = ICD10|E|88|0|e|70
ICD9 = ICD9|273.4
Caption = Structure of
Width = 150
OMIM = 107400
DiseasesDB = 434
MedlinePlus = 000120
eMedicineSubj = med
eMedicineTopic = 108
MeshID = D019896
Alpha 1-antitrypsin deficiency (α1-antitrypsin deficiency, A1AD or Alpha-1) is a
genetic disordercaused by defective production of alpha 1-antitrypsin(A1AT), leading to decreased A1AT activity in the bloodand lungs, and deposition of excessive abnormal A1AT proteinin livercells.cite journal | author = Stoller J, Aboussouan L | title = Alpha1-antitrypsin deficiency | journal = Lancet | volume = 365 | issue = 9478 | pages = 2225–36 | year = 2005| pmid = 15978931 | doi = 10.1016/S0140-6736(05)66781-5] There are several forms and degrees of deficiency. Severe A1A deficiency causes emphysemaand/or COPDin adult life in nearly all people with the condition, as well as various liver diseases in a minority of children and adults, and occasionally more unusual problems.cite journal | author = Needham M, Stockley RA | title = α1-antitrypsin deficiency 3: Clinical manifestations and natural history | journal = Thorax | volume = 59 | issue = | pages = 441–5 | year = 2004 | pmid = 15115878 | doi = 10.1136/thx.2003.006510] It is treated by avoidance of damaging inhalants, by intravenous infusions of the A1AT protein, by transplantation of the liver or lungs, and by a variety of other measures, but it usually produces some degree of disabilityand reduced life expectancyFact|date=August 2008.
Signs and symptoms
Symptoms of alpha-1 antitrypsin deficiency include shortness of breath, wheezing,
rhonchi, and rales. The patient's symptoms may resemble recurrent respiratory infections or asthmathat does not respond to treatment. Individuals with A1AD may develop emphysemaduring their thirties or forties even without a history of significant smoking, though smoking greatly increases the risk for emphysema. A1AD also causes impaired liver function in some patients and may lead to cirrhosisand liver failure(15%). It is the leading cause of liver transplantationin newborns.
alpha 1-antitrypsinfor a discussion of the various genotypes and phenotypes associated with A1AD." Alpha 1-antitrypsin(A1AT) is produced in the liver, and one of its functions is to protect the lungs from the neutrophil elastase enzyme, which can disrupt connective tissue. Normal blood levels of alpha-1 antitrypsin are 1.5-3.5 gm/l. In individuals with PiSS, PiMZ and PiSZ phenotypes, blood levels of A1AT are reduced to between 40 and 60 % of normal levels. This is sufficient to protect the lungs from the effects of elastasein people who do not smoke. However, in individuals with the PiZZ phenotype, A1AT levels are less than 15 % of normal, and patients are likely to develop emphysemaat a young age; 50 % of these patients will develop liver cirrhosis, because the A1AT is not secreted properly and instead accumulates in the liver. A liver biopsyin such cases will reveal PAS-positive, diastase-negative granules. Cigarettesmoke is especially harmful to individuals with A1AD. In addition to increasing the inflammatory reaction in the airways, cigarettesmoke directly inactivates alpha 1-antitrypsinby oxidizing essential methionineresidues to sulfoxideforms, decreasing the enzymeactivity by a factor of 2000.
In the United States, Canada, and several European countries, lung-affected A1AD patients may receive intravenous infusions of alpha-1 antitrypsin, derived from donated human plasma. This augmentation therapy is thought to arrest the course of the disease and halt any further damage to the lungs. Long-term studies of the effectiveness of A1AT replacement therapy are not available. It is currently recommended that patients begin augmentation therapy only after the onset of emphysema symptoms.
Augmentation therapy is not appropriate for liver-affected patients; treatment of A1AD-related liver damage focuses on alleviating the symptoms of the disease. In severe cases, liver transplantation may be necessary.
As α1-antitrypsin is an acute phase reactant, its transcription is markedly increased during
inflammationelsewhere in response to increased interleukin-1 and 6 and TNFα production. Any treatment that blunts this response, specifically paracetamol(acetaminophen), can delay the accumulation of A1AT polymers in the liver and (hence) cirrhosis. A1AD patients are therefore encouraged to use paracetamol when slightly to moderately ill, even if they would otherwise not have used antipyretics.
Treatments currently being studied include recombinant and inhaled forms of A1AT. Other experimental therapies are aimed at the prevention of
polymerformation in the liver.
α1-antitrypsin deficiency has been associated with a number of diseases:
Prolapse[cite journal |author=Chen B, Wen Y, Polan ML |title=Elastolytic activity in women with stress urinary incontinence and pelvic organ prolapse |journal=Neurourol. Urodyn. |volume=23 |issue=2 |pages=119–26 |year=2004 |pmid=14983422 |doi=10.1002/nau.20012 |url=]
Primary sclerosing cholangitis
A1AD was discovered in 1963 by Carl-Bertil Laurell (1919–2001), at the University of Lund, Sweden.cite journal | author = Laurell CB, Eriksson S | title = The electrophoretic alpha 1-globulin pattern of serum in alpha 1-antitrypsin deficiency | journal = Scand J Clin Lab Invest | year = 1963 | volume = 15 | issue = | pages = 132–140 | url= | doi = 10.3109/00365516309051324] Laurell, along with a medical resident, Sten Eriksson, made the discovery after noting the absence of the α1 band on protein
electrophoresisin five of 1500 samples; three of the five patient samples were found to have developed emphysema at a young age.
The link with liver disease was made six years later, when Sharp "et al" described A1AD in the context of liver disease.cite journal | author = Sharp H, Bridges R, Krivit W, Freier E | title = Cirrhosis associated with alpha-1-antitrypsin deficiency: a previously unrecognized inherited disorder | journal = J Lab Clin Med | volume = 73 | issue = 6 | pages = 934–9 | year = 1969 | pmid = 4182334]
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