Genetic variation in aldosterone synthase predicts plasma glucose levels

被引:53
作者
Ranade, K [1 ]
Wu, KD
Risch, N
Olivier, M
Pei, D
Hsiao, CF
Chuang, LM
Ho, LT
Jorgenson, E
Pesich, R
Chen, YDI
Dzau, V
Lin, A
Olshen, RA
Curb, D
Cox, DR
Botstein, D
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[2] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 100, Taiwan
[3] Tri Serv Gen Hosp, Taipei, Taiwan
[4] Natl Hlth Res Inst, Taipei 11529, Taiwan
[5] Vet Gen Hosp, Taipei, Taiwan
[6] Stanford Univ, Sch Med, Div Endocrinol, Stanford, CA 94305 USA
[7] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[8] Hawaii Ctr Hlth Res, Honolulu, HI 96813 USA
关键词
D O I
10.1073/pnas.221467098
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The mineralocorticoid hormone, aldosterone, is known to play a role in sodium homeostasis. We serendipitously found, however, highly significant association between sing le-nucleotide polymorphisms in the alosterone synthase gene and plasma glucose levels in a large population of Chinese and Japanese origin, Two polymorphisms-one in the putative promoter (T-344C) and another resulting in a lysine/arginine substitution at amino acid 173, which are in complete linkage disequilibrium in this population-were associated with fasting plasma glucose levels (P = 0.000017) and those 60 (P = 0.017) and 120 (P = 0.0019) min after an oral glucose challenge. A C/T variant in intron 1, between these polymorphisms, was not associated with glucose levels. Arg-173 and -344C homozygotes were most likely to be diabetic [odds ratio 2.51; 95% confidence interval (C.I.) 1.39-3.92; P = 0.0015] and have impaired fasting glucose levels (odds ratio 3.53; 95% C.I. 2.02-5.5; P = 0.0000036). These results suggest a new role for aldosterone in glucose homeostasis.
引用
收藏
页码:13219 / 13224
页数:6
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