Ho Herbert, Pinto Amar, Hall Stephen D, Flockhart David A, Li Lang, Skaar Todd C, Cadman Peter, O'Connor Daniel T, Wagner Urban, Fineberg Naomi S, Weinberger Myron H
Division of Clinical Pharmacology, Department of Medicine, Indiana University School of Medicine, 1001 W Tenth St, WD Myers Room W7123, Indianapolis, IN 46202, USA.
Hypertension. 2005 Feb;45(2):294-8. doi: 10.1161/01.HYP.0000151361.31736.96. Epub 2004 Dec 13.
We tested the hypothesis that the presence of a CYP3A51 allele is associated with increases in blood pressure in 2 studies of subjects with a total of 683 participants. The first study involving 271 subjects was part of a longitudinal study conducted at Indiana University Medical Center that consisted of 2 phases. The first phase studied the relationship of salt sensitivity with blood pressure, whereas the second phase, conducted approximately 26 years later, studied the relationship between blood pressure, carbohydrate intolerance, and vascular compliance in the same subjects. The second study was a cross-sectional evaluation of 412 normotensive and hypertensive subjects conducted at the University of California San Diego. The second study (Mantel-Haenszel chi(2) test; P=0.05) showed that a greater proportion of black participants with poor blood pressure control had CYP3A51/1 genotype. Evaluation of the untreated blood pressure from phase 1 of the first study showed that the blacks with CYP3A53/*3 (146+/-35 mm Hg) had a higher systolic blood pressure than those with the *1/*3 (119+/-14.1 mm Hg; P=0.0006) and 1/1 (125+/-17.4 mm Hg; P=0.009) genotypes. For blacks in study 2, the CYP3A51 allele was more common in hypertensives (Fisher exact test; P=0.025) than normotensives. In whites there was no association between CYP3A5 genotype and blood pressure in either study. We conclude that although untreated blood pressure may be higher in blacks with the CYP3A53/3 genotype, the CYP3A51 allele may be associated with hypertension that is more refractory to treatment in this ethnic group.
我们在两项共有683名参与者的研究中,对CYP3A51等位基因的存在与血压升高相关这一假设进行了检验。第一项研究涉及271名受试者,是印第安纳大学医学中心进行的一项纵向研究的一部分,该研究包括两个阶段。第一阶段研究盐敏感性与血压的关系,而大约26年后进行的第二阶段研究同一受试者的血压、碳水化合物不耐受和血管顺应性之间的关系。第二项研究是在加利福尼亚大学圣地亚哥分校对412名血压正常和高血压受试者进行的横断面评估。第二项研究(曼特尔 - 亨塞尔χ²检验;P = 0.05)表明,血压控制不佳的黑人参与者中,CYP3A51/1基因型的比例更高。对第一项研究第一阶段未经治疗的血压评估显示,携带CYP3A53/3(146±35 mmHg)的黑人收缩压高于携带1/3(119±14.1 mmHg;P = 0.0006)和1/1(125±17.4 mmHg;P = 0.009)基因型的黑人。在第二项研究中,黑人高血压患者中CYP3A51等位基因比血压正常者更常见(费舍尔精确检验;P = 0.025)。在两项研究中,白人的CYP3A5基因型与血压之间均无关联。我们得出结论,虽然携带CYP3A5*3/3基因型的黑人未经治疗的血压可能更高,但CYP3A51等位基因可能与该种族中更难治疗的高血压相关。