Positive association of CYP11B2 gene polymorphism with genetic predisposition to essential hypertension

被引:51
作者
Tsukada, K
Ishimitsu, T [1 ]
Teranishi, M
Saitoh, M
Yoshii, M
Inada, H
Ohta, S
Akashi, M
Minami, J
Ono, H
Ohrui, M
Matsuoka, H
机构
[1] Dokkyo Univ, Sch Med, Dept Hypertens & Cardiorenal Med, Mibu, Tochigi 3210293, Japan
[2] Dokkyo Univ, Sch Med, Dept Hlth Care, Mibu, Tochigi 3210293, Japan
关键词
essential hypertension; gene polymorphism; aldosterone;
D O I
10.1038/sj.jhh.1001484
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Predispositions to essential hypertension and cardiovascular diseases are possibly associated with gene polymorphisms of the renin-angiotensin system. Gene polymorphisms of angiotensinogen and angiotensin-converting enzyme genes have been suggested to be risk factors for hypertension and myocardial infarction. Concerning the polymorphism of aldosterone synthase (CYP11B2) gene, earlier studies have shown inconsistent results in terms of its relation to hypertension. In the present case-control study, we investigated the association of -344T/C polymorphism in the promoter region of human CYP11B2 gene with genetic predisposition to hypertension. The genotype of -344T/C polymorphism was determined in essential hypertension subjects (n=250) and normotensive subjects (n=221). The distributions of three genotypes (TT, TC, and CC) were significantly different between the hypertensive and the normotensive groups (chi(2) = 9.61, P=0.008). Namely, the frequency of C allele was higher in the hypertensive patients than in the normotensive subjects (34.2 vs 26.5%, P=0.010). Our data suggest that the -344C allele of CYP11B2 gene polymorphism is associated with the genetic predisposition to develop essential hypertension.
引用
收藏
页码:789 / 793
页数:5
相关论文
共 23 条
[1]  
[Anonymous], 1997, ARCH INTERN MED, V157, P2413, DOI DOI 10.1001/ARCHINTE.1997.00440420033005
[2]   Aldosterone synthase gene (CYP11B2) C-344T polymorphism in Caucasians from the Berlin Salt-Sensitivity Trial (BeSST) [J].
Brand, E ;
Schorr, U ;
Ringel, J ;
Beige, J ;
Distler, A ;
Sharma, AM .
JOURNAL OF HYPERTENSION, 1999, 17 (11) :1563-1567
[3]   Structural analysis and evaluation of the aldosterone synthase gene in hypertension [J].
Brand, E ;
Chatelain, N ;
Mulatero, P ;
Féry, I ;
Curnow, K ;
Jeunemaitre, X ;
Corvol, P ;
Pascoe, L ;
Soubrier, F .
HYPERTENSION, 1998, 32 (02) :198-204
[4]  
Chalmers J, 1999, J HYPERTENS, V17, P151
[5]   THE PRODUCT OF THE CYP11B2 GENE IS REQUIRED FOR ALDOSTERONE BIOSYNTHESIS IN THE HUMAN ADRENAL-CORTEX [J].
CURNOW, KM ;
TUSIELUNA, MT ;
PASCOE, L ;
NATARAJAN, R ;
GU, JL ;
NADLER, JL ;
WHITE, PC .
MOLECULAR ENDOCRINOLOGY, 1991, 5 (10) :1513-1522
[6]   Aldosterone excretion rate and blood pressure in essential hypertension are related to polymorphic differences in the aldosterone synthase gene CYP11B2 [J].
Davies, E ;
Holloway, CD ;
Ingram, MC ;
Inglis, GC ;
Friel, EC ;
Morrison, C ;
Anderson, NH ;
Fraser, R ;
Connell, JMC .
HYPERTENSION, 1999, 33 (02) :703-707
[7]   Genetic variation in P450c11AS in Chilean patients with low renin hypertension [J].
Fardella, CE ;
Rodriguez, H ;
Montero, J ;
Zhang, GR ;
Vignolo, P ;
Rojas, A ;
Villarroel, L ;
Miller, WL .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1996, 81 (12) :4347-4351
[8]   Joint effects of an aldosterone synthase (CYP11B2) gene polymorphism and classic risk factors on risk of myocardial infarction [J].
Hautanen, A ;
Toivanen, P ;
Mänttäri, M ;
Tenkanen, L ;
Kupari, M ;
Manninen, V ;
Kayes, KM ;
Rosenfeld, S ;
White, PC .
CIRCULATION, 1999, 100 (22) :2213-2218
[9]   Associations between aldosterone synthase gene polymorphism and the adrenocortical function in males [J].
Hautanen, A ;
Lankinen, L ;
Kupari, M ;
Jänne, OA ;
Adlercreutz, H ;
Nikkilä, H ;
White, PC .
JOURNAL OF INTERNAL MEDICINE, 1998, 244 (01) :11-18
[10]   Evaluation of the aldosterone synthase (CYP11B2) gene polymorphism in patients with myocardial infarction [J].
Hengstenberg, C ;
Holmer, SR ;
Mayer, B ;
Löwel, H ;
Engel, S ;
Hense, HW ;
Riegger, GAJ ;
Schunkert, H .
HYPERTENSION, 2000, 35 (03) :704-709