Identification of individuals with alpha-1-antitrypsin deficiency by a targeted screening program

被引:53
作者
Bals, Robert
Koczulla, Rembert
Kotke, Viktor
Andress, Juergen
Blackert, Karlheinz
Vogelmeier, Claus
机构
[1] Univ Marburg, Hosp Univ Marburg, Div Pulm Dis, Dept Internal Med, D-35043 Marburg, Germany
[2] Agcy KONSENS, D-59368 Werne, Germany
关键词
alpha-1 antitrypsin deficiency; chronic obstructive pulmonary disease; genetic diagnosis; liver disease;
D O I
10.1016/j.rmed.2007.02.024
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Alpha-1-antitrypsin deficiency (AATD) is significantly underdiagnosed. The early detection of AATD would enable affected persons to make lifestyle changes such as quitting smoking. It was the aim of the study to determine whether the combination of an awareness program with the offer of a cost-free diagnostic test results in the identification of a significant number of individuals with severe AATD. Methodology: We combined a series of measures to promote awareness with the offer of a diagnostic test at no charge. Test blood was applied to a fitter paper and sent to our laboratory. The level of AAT was measured by nephelometry, the presence of the S- or Z-allele was determined by PCR, and phenotyping was performed by isoelectric focusing. Results: During 37 months 17688 testing kits were distributed and 2722 were sent back to our laboratory. We identified 335 patients with severe AATD including 16 individuals with rare genotypes. Prescreening by determining the AAT serum levels by the submitting physician increased the detection rate as compared to similar programs that screened unsetected individuals. Summary: These data show that the combination of an awareness program with the offer of free diagnostic testing results in the identification of a large number individuals with severe AATD. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1708 / 1714
页数:7
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