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CYP11B2基因多态性决定日本人的盐敏感性。

Polymorphism of CYP11B2 determines salt sensitivity in Japanese.

作者信息

Iwai Naoharu, Kajimoto Kazuaki, Tomoike Hitonobu, Takashima Naoyuki

机构信息

Department of Epidemiology, National Cardiovascular Center, Suita, Osaka, Japan.

出版信息

Hypertension. 2007 Apr;49(4):825-31. doi: 10.1161/01.HYP.0000258796.52134.26. Epub 2007 Feb 12.

Abstract

Aldosterone plays essential roles in body fluid and electrolyte homeostasis and blood pressure. However, the association between polymorphisms in the CYP11B2 gene and hypertension is controversial. We resequenced CYP11B1 and CYP11B2 and identified 35 polymorphisms in this region. We performed association studies between the plasma aldosterone concentration and 13 polymorphisms in this region in 1443 subjects. The subjects were all obtained from the Suita Cohort Study. Multiple regression analysis indicated that aldosterone levels were determined by renin activity, age, total cholesterol, and hematocrit. Residuals of the aldosterone levels after adjusting for these confounding factors were nominally associated with the T(-344)C (P=0.0026), C(595)T (P=0.0180), -(4837)C (P=0.0310), and G(4936)A (P=0.0498) polymorphisms. Only the T(-344)C polymorphism was significantly associated with the aldosterone level after a correction for multiple testing (Bonferroni). A significant interaction was observed between the T(-344)C polymorphism and renin activity in determining aldosterone levels. Moreover, a significant interaction was observed in 2063 subjects between urinary sodium excretion, which reflects sodium intake, and the T(-344)C polymorphism in determining systolic blood pressure. Only subjects with the TT genotype showed a positive correlation between urinary sodium excretion and systolic blood pressure. In vitro experiments confirmed the functional significance of this T(-344)C polymorphism in terms of angiotensin II reactivity. Thus, the T(-344)C polymorphism in CYP11B2 appears to affect salt sensitivity in Japanese and to have clinical significance.

摘要

醛固酮在体液、电解质平衡及血压调节中发挥着重要作用。然而,CYP11B2基因多态性与高血压之间的关联仍存在争议。我们对CYP11B1和CYP11B2进行了重测序,并在该区域鉴定出35个多态性位点。我们在1443名受试者中对血浆醛固酮浓度与该区域的13个多态性位点进行了关联研究。所有受试者均来自吹田队列研究。多元回归分析表明,醛固酮水平由肾素活性、年龄、总胆固醇和血细胞比容决定。校正这些混杂因素后,醛固酮水平的残差与T(-344)C(P = 0.0026)、C(595)T(P = 0.0180)、-(4837)C(P = 0.0310)和G(4936)A(P = 0.0498)多态性存在名义上的关联。经过多重检验校正(Bonferroni法)后,只有T(-344)C多态性与醛固酮水平显著相关。在决定醛固酮水平方面,观察到T(-344)C多态性与肾素活性之间存在显著的相互作用。此外,在2063名受试者中,反映钠摄入的尿钠排泄与T(-344)C多态性在决定收缩压方面存在显著的相互作用。只有TT基因型的受试者尿钠排泄与收缩压呈正相关。体外实验证实了该T(-344)C多态性在血管紧张素II反应性方面的功能意义。因此,CYP11B2基因中的T(-344)C多态性似乎影响日本人的盐敏感性,并具有临床意义。

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