Program in Medical and Population Genetics and the Cardiovascular Disease Initiative, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.
Cardiovascular Research Center, Massachusetts General Hospital, Boston.
JAMA Cardiol. 2022 Nov 1;7(11):1129-1137. doi: 10.1001/jamacardio.2022.3191.
Hypertension remains the major cardiovascular disease risk factor globally, but variability in measured blood pressure may result in suboptimal management. Whether genetic contributors to elevated blood pressure may complementarily inform cardiovascular disease risk assessment is unknown.
To examine incident cardiovascular disease by blood pressure polygenic risk score independent of measured blood pressures and antihypertensive medication prescriptions.
DESIGN, SETTING, AND PARTICIPANTS: The cohort study (UK Biobank) recruited UK residents aged 40 to 69 years between March 2006 and August 2010. Participants without a prior physician diagnosis of cardiovascular disease, including myocardial infarction, stroke, or heart failure, were included. Excluded were individuals with mismatch between self-reported and genotypically inferred sex, sex aneuploidy, missing genotype rates of 1% or greater, and excess genotypic heterozygosity. Data analyses were performed from September 25, 2021, to July 21, 2022.
Measured blood pressure and externally derived blood pressure polygenic risk score stratified by hypertension diagnosis and management, which included normal blood pressure (<130/80 mm Hg without antihypertensives), untreated hypertension (systolic blood pressure ≥130 mm Hg or diastolic blood pressure ≥80 mm Hg without antihypertensives), and treated hypertension (current antihypertensives prescriptions).
Composite of first incident myocardial infarction, stroke, heart failure, or cardiovascular-related death.
Of the 331 078 study participants included (mean [SD] age at enrollment, 56.9 [8.1] years; 178 824 female [54.0%]), 83 094 (25.1%) had normal blood pressure, 197 597 (59.7%) had untreated hypertension, and 50 387 (15.2%) had treated hypertension. Over a median (IQR) follow-up of 11.1 (10.4-11.8) years, the primary outcome occurred in 15 293 participants. Among those with normal blood pressure, untreated hypertension, and treated hypertension, each SD increase in measured systolic blood pressure was associated with hazard ratios of 1.08 (95% CI, 0.93-1.25), 1.20 (95% CI, 1.16-1.23), and 1.16 (95% CI, 1.11-1.20), respectively, for the primary outcome. Among these same categories, each SD increase in genetically predicted systolic blood pressure was associated with increased hazard ratios of 1.13 (95% CI, 1.05-1.20), 1.04 (95% CI, 1.01-1.07), and 1.06 (95% CI, 1.02-1.10), respectively, for the primary outcome independent of measured blood pressures and other covariates. Findings were similar for measured and genetically predicted diastolic blood pressure.
Blood pressure polygenic risk score may augment identification of individuals at heightened cardiovascular risk, including those with both normal blood pressure and hypertension. Whether it may also guide antihypertensive initiation or intensification requires further study.
高血压仍然是全球主要的心血管疾病风险因素,但测量血压的变化可能导致管理效果不佳。遗传因素是否会补充血压升高对心血管疾病风险评估的信息尚不清楚。
通过独立于测量血压和降压药物处方的血压多基因风险评分来检测心血管疾病的发病情况。
设计、设置和参与者:这项队列研究(英国生物库)于 2006 年 3 月至 2010 年 8 月期间招募了年龄在 40 至 69 岁之间的英国居民。研究对象包括没有心血管疾病(包括心肌梗死、中风或心力衰竭)的医生诊断史。排除了自我报告和基因推断性别之间不匹配、性染色体非整倍体、基因型缺失率大于 1%以及基因型杂合度过高的个体。数据分析于 2021 年 9 月 25 日至 2022 年 7 月 21 日进行。
测量血压和外部衍生的血压多基因风险评分,按高血压诊断和管理进行分层,包括正常血压(<130/80mmHg 且未服用降压药)、未治疗的高血压(收缩压≥130mmHg 或舒张压≥80mmHg 且未服用降压药)和治疗的高血压(目前服用降压药)。
首次发生心肌梗死、中风、心力衰竭或心血管相关死亡的复合终点。
在纳入的 331078 名研究参与者中(入组时的平均[标准差]年龄为 56.9[8.1]岁;178824 名女性[54.0%]),83094 名(25.1%)参与者血压正常,197597 名(59.7%)未治疗的高血压患者,50387 名(15.2%)为治疗的高血压患者。在中位数(IQR)随访 11.1(10.4-11.8)年后,15293 名参与者发生了主要结局。在血压正常、未治疗的高血压和治疗的高血压患者中,每增加一个标准差的测量收缩压与主要结局的风险比分别为 1.08(95%CI,0.93-1.25)、1.20(95%CI,1.16-1.23)和 1.16(95%CI,1.11-1.20)。在这些相同类别中,每增加一个标准差的遗传预测收缩压与主要结局的风险比分别为 1.13(95%CI,1.05-1.20)、1.04(95%CI,1.01-1.07)和 1.06(95%CI,1.02-1.10),这与独立于测量血压和其他协变量的主要结局相关。测量和遗传预测舒张压的结果相似。
血压多基因风险评分可能会增加对心血管风险升高个体的识别,包括血压正常和高血压患者。它是否也可以指导降压药物的起始或强化治疗还需要进一步研究。