The prevalence of alpha-1 antitrypsin deficiency in Ireland
<p>Abstract</p> <p>Background</p> <p>Alpha-1 antitrypsin deficiency (AATD) results from mutations in the SERPINA1 gene and classically presents with early-onset emphysema and liver disease. The most common mutation presenting with clinical evidence is the Z mutation, wh...
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doaj-a7f5e10760d04bd4b05fc6d1492048dd2020-11-24T22:16:06ZengBMCRespiratory Research1465-99212011-07-011219110.1186/1465-9921-12-91The prevalence of alpha-1 antitrypsin deficiency in IrelandMorris Valerie BDimitrov Borislav DO'Brien GeraldineKelleher Dermot PMcPartlin JosephFloyd OlwenO'Connor Catherine ACarroll Tomás PTaggart Clifford CMcElvaney Noel G<p>Abstract</p> <p>Background</p> <p>Alpha-1 antitrypsin deficiency (AATD) results from mutations in the SERPINA1 gene and classically presents with early-onset emphysema and liver disease. The most common mutation presenting with clinical evidence is the Z mutation, while the S mutation is associated with a milder plasma deficiency. AATD is an under-diagnosed condition and the World Health Organisation recommends targeted detection programmes for AATD in patients with chronic obstructive pulmonary disease (COPD), non-responsive asthma, cryptogenic liver disease and first degree relatives of known AATD patients.</p> <p>Methods</p> <p>We present data from the first 3,000 individuals screened following ATS/ERS guidelines as part of the Irish National Targeted Detection Programme (INTDP). We also investigated a DNA collection of 1,100 individuals randomly sampled from the general population. Serum and DNA was collected from both groups and mutations in the SERPINA1 gene detected by phenotyping or genotyping.</p> <p>Results</p> <p>The Irish National Targeted Detection Programme identified 42 ZZ, 44 SZ, 14 SS, 430 MZ, 263 MS, 20 IX and 2 rare mutations. Analysis of 1,100 randomly selected individuals identified 113 MS, 46 MZ, 2 SS and 2 SZ genotypes.</p> <p>Conclusion</p> <p>Our findings demonstrate that AATD in Ireland is more prevalent than previously estimated with Z and S allele frequencies among the highest in the world. Furthermore, our targeted detection programme enriched the population of those carrying the Z but not the S allele, suggesting the Z allele is more important in the pathogenesis of those conditions targeted by the detection programme.</p> http://respiratory-research.com/content/12/1/91 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Morris Valerie B Dimitrov Borislav D O'Brien Geraldine Kelleher Dermot P McPartlin Joseph Floyd Olwen O'Connor Catherine A Carroll Tomás P Taggart Clifford C McElvaney Noel G |
spellingShingle |
Morris Valerie B Dimitrov Borislav D O'Brien Geraldine Kelleher Dermot P McPartlin Joseph Floyd Olwen O'Connor Catherine A Carroll Tomás P Taggart Clifford C McElvaney Noel G The prevalence of alpha-1 antitrypsin deficiency in Ireland Respiratory Research |
author_facet |
Morris Valerie B Dimitrov Borislav D O'Brien Geraldine Kelleher Dermot P McPartlin Joseph Floyd Olwen O'Connor Catherine A Carroll Tomás P Taggart Clifford C McElvaney Noel G |
author_sort |
Morris Valerie B |
title |
The prevalence of alpha-1 antitrypsin deficiency in Ireland |
title_short |
The prevalence of alpha-1 antitrypsin deficiency in Ireland |
title_full |
The prevalence of alpha-1 antitrypsin deficiency in Ireland |
title_fullStr |
The prevalence of alpha-1 antitrypsin deficiency in Ireland |
title_full_unstemmed |
The prevalence of alpha-1 antitrypsin deficiency in Ireland |
title_sort |
prevalence of alpha-1 antitrypsin deficiency in ireland |
publisher |
BMC |
series |
Respiratory Research |
issn |
1465-9921 |
publishDate |
2011-07-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Alpha-1 antitrypsin deficiency (AATD) results from mutations in the SERPINA1 gene and classically presents with early-onset emphysema and liver disease. The most common mutation presenting with clinical evidence is the Z mutation, while the S mutation is associated with a milder plasma deficiency. AATD is an under-diagnosed condition and the World Health Organisation recommends targeted detection programmes for AATD in patients with chronic obstructive pulmonary disease (COPD), non-responsive asthma, cryptogenic liver disease and first degree relatives of known AATD patients.</p> <p>Methods</p> <p>We present data from the first 3,000 individuals screened following ATS/ERS guidelines as part of the Irish National Targeted Detection Programme (INTDP). We also investigated a DNA collection of 1,100 individuals randomly sampled from the general population. Serum and DNA was collected from both groups and mutations in the SERPINA1 gene detected by phenotyping or genotyping.</p> <p>Results</p> <p>The Irish National Targeted Detection Programme identified 42 ZZ, 44 SZ, 14 SS, 430 MZ, 263 MS, 20 IX and 2 rare mutations. Analysis of 1,100 randomly selected individuals identified 113 MS, 46 MZ, 2 SS and 2 SZ genotypes.</p> <p>Conclusion</p> <p>Our findings demonstrate that AATD in Ireland is more prevalent than previously estimated with Z and S allele frequencies among the highest in the world. Furthermore, our targeted detection programme enriched the population of those carrying the Z but not the S allele, suggesting the Z allele is more important in the pathogenesis of those conditions targeted by the detection programme.</p> |
url |
http://respiratory-research.com/content/12/1/91 |
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