Variation at the aldosterone synthase (CYP11B2) locus contributes to hypertension in subjects with a raised aldosterone-to-renin ratio

被引:85
作者
Lim, PO [1 ]
MacDonald, TM
Holloway, C
Friel, E
Anderson, NH
Dow, E
Jung, RT
Davies, E
Fraser, R
Connell, JMC
机构
[1] Univ Wales Coll Med, Heart Res Inst, Dept Cardiol, Cardiff CF14 4XN, S Glam, Wales
[2] Ninewells Hosp & Med Sch, Hypertens Res Ctr, Dundee DD1 9SY, Scotland
[3] Ninewells Hosp & Med Sch, Directorate Biochem Med, Dundee DD1 9SY, Scotland
[4] Ninewells Hosp & Med Sch, Dept Endocrinol, Dundee DD1 9SY, Scotland
[5] Western Infirm & Associated Hosp, MRC, Blood Pressure Grp, Glasgow G11 6NT, Lanark, Scotland
关键词
D O I
10.1210/jc.2001-012070
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aldosterone-to-renin ratio (ARR) is a marker of aldosterone activity in hypertension. We examined the relationship of the ARR to the distribution of two biallelic polymorphisms at the CYP11B2 gene locus. One polymorphism affects a putative steroidogenic factor-1 binding site (-344 T/C) in the 5'-regulatory region, whereas the other marker reflects replacement of the intron-2 from CYP11B2 with that from the neighboring gene encoding 11beta-hydroxylase (CYP11B1; wildtype/conversion). We studied consecutive referrals to the Tayside hypertension clinic in 1998. Because the specificity of ARR (pmol/liter/ng/ml/h) for hyperaldosteronism. increases with its threshold, ARRs of at least 750 and 1000 were used. A total of 375 patients were assessed; 86.9% had complete data. There were significant excesses of steroidogenic factor-1 (T) (ARR greater than or equal to750, 0.62 vs. 0.51, P = 0.014; ARR greater than or equal to 1000, 0.63 vs. 0.51, P = 0.039) and intron-2 (conversion) (ARR greater than or equal to 750, 0.49 vs. 0.41, P = 0.205; ARR greater than or equal to 1000, 0.54 vs. 0.41, P = 0.029) alleles inpatients with a raised ARR. The odds ratio for a raised ARR was 2.27 [95% confidence interval, 1.01, 5.09; P < 0.05] comparing patients with a homozygous haplotype for these alleles with those without any such alleles, and this risk increased with age. This study supports the notion that there is a genetic component that regulates aldosterone production and that hyperaldosteronism might develop over time in susceptible individuals.
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收藏
页码:4398 / 4402
页数:5
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