Prevalence of alpha-1 antitrypsin deficiency in poorly controlled asthma - Results from the ALA-ACRC low-dose theophylline trial

被引:17
作者
Eden, E.
Holbrook, J. T.
Brantly, M. L.
Turino, G. M.
Wise, R. A.
机构
[1] Columbia Univ, St Lukes Roosevelt Hosp, Div Pulm & Crit Care Med MU316, New York, NY 10025 USA
[2] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[3] Univ Florida, Gainesville, FL USA
[4] Johns Hopkins Asthma & Allergy Ctr, Baltimore, MD USA
[5] Amer Lung Assoc, Asthma Clin Res Ctr, New York, NY 10019 USA
关键词
asthma; alpha-1 antitrypsin deficiency; genetic screening; ALPHA-1; ANTITRYPSIN; INHIBITOR; DEFICIENCY; PHENOTYPES; ALPHA(1)-ANTITRYPSIN; EMPHYSEMA; VARIANTS; CHILDREN; LUNG;
D O I
10.1080/02770900701540028
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
In a study comparing low-dose theophylline to montelukast in poorly controlled asthmatics, 285 subjects consented to be screened for alpha-1 antitrypsin deficiency. Of the 284 for which complete data was available, 10.5% carried a deficiency gene and 2.4% were mildly deficient with an alpha-1 antitrypsin serum level of less than 20 mu M. In the non-African-American cohort, an abnormal phenotype occurred in 12% and 2.9% were mildly deficient. Baseline pulmonary function and asthma scores were not significantly different between those with normal and abnormal AAT phenotype. However those with the deficiency tended to show a greater bronchodilator response.
引用
收藏
页码:605 / 608
页数:4
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