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. 2015 Nov;51(11):539-43.
doi: 10.1016/j.arbres.2015.01.008. Epub 2015 Mar 21.

Alpha-1 Antitrypsin Deficiency in COPD Patients: A Cross-Sectional Study (V体育ios版)

[Article in English, Spanish]
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Alpha-1 Antitrypsin Deficiency in COPD Patients: A Cross-Sectional Study

[Article in English, Spanish]
Patricia Beatriz Sorroche et al. Arch Bronconeumol. 2015 Nov.

Abstract

Introduction: Alpha-1 antitrypsin deficiency (AATD) is a genetic disorder associated with early onset chronic obstructive pulmonary disease (COPD) and liver disease VSports手机版. It is also a highly under-diagnosed condition. As early diagnosis could prompt specific interventions such as smoking cessation, testing of family members, genetic counselling and use of replacement therapy, screening programs are needed to identify affected patients. .

Objective: To estimate the prevalence of severe AATD in COPD patients by routine dried blood spot testing and subsequent genotyping in patients with alpha-1 antitrypsin (AAT) levels below an established threshold. V体育安卓版.

Materials and methods: Cross-sectional study of adult COPD patients attending the Hospital Dr. Antonio Cetrángolo (Buenos Aires, Argentina) between 2009 and 2012 V体育ios版. The study consisted of capillary blood collection via finger stick to determine AAT levels, clinical evaluation and lung function tests. Genotype was determined in AAT-deficient patients. .

Results: A total of 1,002 patients were evaluated, of whom 785 (78. 34%) had normal AAT levels, while low AAT levels were found in 217 (21. 66%). Subsequent genotyping of the latter sub-group found: 15 (1. 5%, 95% CI 0. 75-2. 25) patients with a genotype associated with severe AATD, of whom 12 were ZZ (1. 2%, 95% CI 0. 52-1. 87) and 3 SZ (0. 3%, 95% CI 0-0. 64). The remaining 202 patients were classified as: 29 Z heterozygotes (2. 89%, 95% CI 1 VSports最新版本. 86-3. 93), 25 S heterozygotes (2. 5%, 95% CI 1. 53-3. 46) and 4 SS (0. 4%, 95% CI 0. 01-0. 79). A definitive diagnosis could not be reached in 144 patients (14. 37%, 95% CI 12. 2-16. 54). .

Conclusion: The strategy using an initial serum AAT level obtained by dried blood spot testing and subsequent genotyping was a satisfactory initial approach to a screening program for severe AAT, as a definitive diagnosis was achieved in 87% of patients. However, results were not obtained for logistical reasons in the remaining 13%. This major obstacle may be overcome by the use of dried blood spot phenotyping techniques V体育平台登录. We believe this approach for detecting AATD in COPD patients, in compliance with national and international guidelines, is supported by our results. .

Keywords: Alpha-1 antitrypsin deficiency; Chronic obstructive pulmonary disease; Dried blood spot testing; Déficit de alfa 1 antitripsina; Enfermedad pulmonar obstructiva crónica; Medición de la concentración de proteína en sangre seca VSports注册入口. .

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