Evaluation of the angiotensinogen locus in human essential hypertension - A European study

被引:83
作者
Brand, E
Chatelain, N
Keavney, B
Caulfield, M
Citterio, L
Connell, J
Grobbee, D
Schmidt, S
Schunkert, H
Schuster, H
Sharma, AM
Soubrier, F
机构
[1] Hop St Louis, INSERM U358, F-75475 Paris 10, France
[2] Univ Milan, Hosp San Raffaele, Div Nephrol & Hypertens, I-20122 Milan, Italy
[3] St Bartholomews Hosp, Dept Clin Pharmacol, London, England
[4] Wellcome Trust Ctr Human Genet, Oxford, England
[5] Univ Glasgow, Western Infirm, Dept Med & Therapeut, Glasgow G11 6NT, Lanark, Scotland
[6] Erasmus Univ, Sch Med, Dept Epidemiol & Biostat, NL-3000 DR Rotterdam, Netherlands
[7] Univ Heidelberg, Dept Internal Med, Heidelberg, Germany
[8] Univ Regensburg, Dept Internal Med, Regensburg, Germany
[9] Humboldt Univ, Dept Internal Med, Franz Volhard Clin, Berlin, Germany
[10] Univ Berlin, Clin Benjamin Franklin, Dept Internal Med, Berlin, Germany
基金
英国惠康基金;
关键词
angiotensinogen; hypertension; essential; genetics; microsatellite repeats;
D O I
10.1161/01.HYP.31.3.725
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Different family and case-control studies support genetic linkage and association at the human angiotensinogen (AGT) locus with essential hypertension. To extend these previous observations, a European collaborative study of nine centers was set up to create a large resource of affected sibling pairs. The AGT locus was studied using a highly polymorphic dinucleotide repeat in the 3'-flanking region of the gene in 350 European families, comprising 630 affected sibling pairs. Statistical analyses using two different methods did not show any evidence for linkage either in the whole panel or in family subsets selected for severity or early onset of disease. Although several arguments from association studies suggest a role of the AGT gene in essential hyper-tension, this large family study did not replicate the initial linkage reported smaller studies. Our results highlight the difficulty of identifying susceptibility genes by linkage analysis in complex diseases.
引用
收藏
页码:725 / 729
页数:5
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