Bochud Murielle, Bovet Pascal, Elston Robert C, Paccaud Fred, Falconnet Catherine, Maillard Marc, Shamlaye Conrad, Burnier Michel
Department of Epidemiology and Biostatistics, Case Western Reserve University, Cleveland, Ohio, USA.
Hypertension. 2005 Mar;45(3):445-50. doi: 10.1161/01.HYP.0000156538.59873.86. Epub 2005 Feb 7.
We estimated the heritability of ambulatory systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse pressure (PP) in east African families with at least 2 hypertensive siblings and living in the Seychelles islands (Indian Ocean). The sample consisted of 314 individuals (147 men and 167 women), both normotensive and hypertensive, from 76 pedigrees (mean+/-SD of 4.1+/-2.8 persons per pedigree). After a 2-week off-treatment period, daytime and nighttime ambulatory blood pressure (BP) was monitored. Office BP was measured with a standard mercury sphygmomanometer. We estimated by maximum likelihood the age- and sex-adjusted heritabilities from the additive polygenic component of the variance of the traits allowing for the presence of other familial correlations. We also adjusted for ascertainment (ie, for the fact that 2 siblings had to be hypertensive) and examined the effect of adjusting for body mass index, 24-hour urinary excretion of sodium and potassium, plasma renin activity, and plasma aldosterone concentration. Heritability estimates (+/-SE) for ambulatory SBP, DBP, and PP were, respectively, 0.37+/-0.12/0.24+/-0.12/0.54+/-0.12 for daytime and 0.34+/-0.13/ 0.37+/-0.15/0.47+/-0.12 for nighttime measurements (P<0.05 for all estimates). Heritability estimates for office SBP, DBP, and PP were, respectively, 0.20+/-0.11, 0.05+/-0.09, and 0.37+/-0.12. Heritability estimates for SBP varied markedly according to whether participants were treated for hypertension at baseline. The present data show that ambulatory BP and PP have a high heritability in families of African descent. They also demonstrate that antihypertensive treatment and the number of BP measurements have a major influence on the heritability estimates.
我们估算了居住在塞舌尔群岛(印度洋)、至少有两名高血压同胞的东非家庭中动态收缩压(SBP)、舒张压(DBP)和脉压(PP)的遗传度。样本包括来自76个家系的314名个体(147名男性和167名女性),有血压正常者和高血压患者(每个家系平均4.1±2.8人)。经过2周的停药期后,监测白天和夜间的动态血压(BP)。诊室血压用标准汞柱血压计测量。我们通过最大似然法,从性状方差的加性多基因成分中估算年龄和性别校正后的遗传度,同时考虑其他家族相关性的存在。我们还对确定因素进行了校正(即两名同胞必须为高血压这一事实),并研究了校正体重指数、24小时尿钠和钾排泄量、血浆肾素活性以及血浆醛固酮浓度的影响。白天动态SBP、DBP和PP的遗传度估计值(±SE)分别为0.37±0.12/0.24±0.12/0.54±0.12,夜间测量值分别为0.34±0.13/0.37±0.15/0.47±0.12(所有估计值P<0.05)。诊室SBP、DBP和PP的遗传度估计值分别为0.20±0.11、0.05±0.09和0.37±0.12。根据参与者在基线时是否接受高血压治疗,SBP的遗传度估计值有显著差异。目前的数据表明,非洲裔家庭中动态血压和脉压具有较高的遗传度。它们还表明,降压治疗和血压测量次数对遗传度估计值有重大影响。