Summary
Among 20 individuals with severeα 1 antitrypsin (α1AT) deficiency we observed extremely variable clinical phenotypes ranging from rapidly progressive lung disease fatal at the age of 42 years to an asymptomatic individual with normal lung function at the age of 50 years. Eighteen subjects, including the asymptomatic one, carried the deficient Pi ZZ phenotype as determined by isoelectric focusing (IEF). Their meanα1AT serum level was 36.7±7.7 mg/dl. DNA restriction analysis showed that all of them had the classical Pi Z-allele-associated DNA haplotype, thus confirming the IEF data. Obviously not all Pi ZZ individuals will have clinical sequelae caused by this genotype. The important differences in clinical course observed could not be explained by smoking habits alone. Probably additional factors are pertinent to the pathogenesis of the lung disease associated withα1AT deficiency (defects in other genes, environmental influences other than smoking). In two patients with very lowα1AT serum levels definitive phenotyping by IEF was not possible. Therefore we investigated the molecular basis of their deficiency using polymerase chain reaction (PCR) amplification of the coding exons of theirα1AT genes and direct sequencing of the amplification products. Sequence data analysis showed that one of these patients, who had initially been phenotyped as Pi ZZ by IEF, had in fact the genotype Pi QObellinghamZ, thus explaining her lowα1AT serum level of 20 mg/dl. The other patient (α1AT serum level 3.7 mg/dl) exhibited the rare genotype Pi MheerlenQOgranite falls. Despite his nearly completeα1AT deficiency, he suffered from only moderately severe pulmonary disease at the age of 42 years.
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Abbreviations
- α1AT:
-
α 1-antitrypsin
- IEF:
-
isoelectric focusing
- Pi:
-
proteinase inhibitor phenotype
- PCR:
-
polymerase chain reaction
- COPD:
-
chronic obstructive pulmonary disease
- IGV:
-
intrathoracic gas volume
- Raw :
-
airway resistance
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Poller, W., Faber, J.P. & Olek, K. Highly variable clinical course in severeα 1-antitrypsin deficiency — Use of polymerase chain reaction for the detection of rare deficiency alleles. Klin Wochenschr 68, 857–863 (1990). https://doi.org/10.1007/BF01662782
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DOI: https://doi.org/10.1007/BF01662782