Ference Brian A, Bhatt Deepak L, Catapano Alberico L, Packard Chris J, Graham Ian, Kaptoge Stephen, Ference Thatcher B, Guo Qi, Laufs Ulrich, Ruff Christian T, Cupido Arjen, Hovingh G Kees, Danesh John, Holmes Michael V, Smith George Davey, Ray Kausik K, Nicholls Stephen J, Sabatine Marc S
Centre for Naturally Randomized Trials, University of Cambridge, Cambridge, United Kingdom.
MRC/BHF Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, University of Cambridge, Cambridge, United Kingdom.
JAMA. 2019 Oct 8;322(14):1381-1391. doi: 10.1001/jama.2019.14120.
The relationship between exposure to lower low-density lipoprotein cholesterol (LDL-C) and lower systolic blood pressure (SBP) with the risk of cardiovascular disease has not been reliably quantified.
To assess the association of lifetime exposure to the combination of both lower LDL-C and lower SBP with the lifetime risk of cardiovascular disease.
DESIGN, SETTING, AND PARTICIPANTS: Among 438 952 participants enrolled in the UK Biobank between 2006 and 2010 and followed up through 2018, genetic LDL-C and SBP scores were used as instruments to divide participants into groups with lifetime exposure to lower LDL-C, lower SBP, or both. Differences in plasma LDL-C, SBP, and cardiovascular event rates between the groups were compared to estimate associations with lifetime risk of cardiovascular disease.
Differences in plasma LDL-C and SBP compared with participants with both genetic scores below the median. Genetic risk scores higher than the median were associated with lower LDL-C and lower SBP.
Odds ratio (OR) for major coronary events, defined as coronary death, nonfatal myocardial infarction, or coronary revascularization.
The mean age of the 438 952 participants was 65.2 years (range, 40.4-80.0 years), 54.1% were women, and 24 980 experienced a first major coronary event. Compared with the reference group, participants with LDL-C genetic scores higher than the median had 14.7-mg/dL lower LDL-C levels and an OR of 0.73 for major coronary events (95% CI, 0.70-0.75; P < .001). Participants with SBP genetic scores higher than the median had 2.9-mm Hg lower SBP and an OR of 0.82 for major coronary events (95% CI, 0.79-0.85, P < .001). Participants in the group with both genetic scores higher than the median had 13.9-mg/dL lower LDL-C, 3.1-mm Hg lower SBP, and an OR of 0.61 for major coronary events (95% CI, 0.59-0.64; P < .001). In a 4 × 4 factorial analysis, exposure to increasing genetic risk scores and lower LDL-C levels and SBP was associated with dose-dependent lower risks of major coronary events. In a meta-regression analysis, combined exposure to 38.67-mg/dL lower LDL-C and 10-mm Hg lower SBP was associated with an OR of 0.22 for major coronary events (95% CI, 0.17-0.26; P < .001), and 0.32 for cardiovascular death (95% CI, 0.25-0.40; P < .001).
Lifelong genetic exposure to lower levels of low-density lipoprotein cholesterol and lower systolic blood pressure was associated with lower cardiovascular risk. However, these findings cannot be assumed to represent the magnitude of benefit achievable from treatment of these risk factors.
较低的低密度脂蛋白胆固醇(LDL-C)水平和较低的收缩压(SBP)与心血管疾病风险之间的关系尚未得到可靠量化。
评估终生暴露于较低LDL-C和较低SBP的组合与心血管疾病终生风险之间的关联。
设计、设置和参与者:在2006年至2010年纳入英国生物银行并随访至2018年的438952名参与者中,使用遗传LDL-C和SBP评分作为工具,将参与者分为终生暴露于较低LDL-C、较低SBP或两者的组。比较各组之间血浆LDL-C、SBP和心血管事件发生率的差异,以估计与心血管疾病终生风险的关联。
与两个遗传评分均低于中位数的参与者相比,血浆LDL-C和SBP的差异。高于中位数的遗传风险评分与较低的LDL-C和较低的SBP相关。
主要冠状动脉事件的比值比(OR),定义为冠状动脉死亡、非致命性心肌梗死或冠状动脉血运重建。
438952名参与者的平均年龄为65.2岁(范围40.4 - 80.0岁),54.1%为女性,24980人经历了首次主要冠状动脉事件。与参照组相比,LDL-C遗传评分高于中位数的参与者LDL-C水平低14.7mg/dL,主要冠状动脉事件的OR为0.73(95%CI,0.70 - 0.75;P <.001)。SBP遗传评分高于中位数的参与者SBP低2.9mmHg,主要冠状动脉事件的OR为0.82(95%CI,0.79 - 0.85,P <.001)。两个遗传评分均高于中位数的组中的参与者LDL-C低13.9mg/dL,SBP低3.1mmHg,主要冠状动脉事件的OR为0.61(95%CI,0.59 - 0.64;P <.001)。在4×4析因分析中,暴露于增加的遗传风险评分以及较低的LDL-C水平和SBP与主要冠状动脉事件风险呈剂量依赖性降低相关。在荟萃回归分析中,联合暴露于LDL-C低38.67mg/dL和SBP低10mmHg与主要冠状动脉事件的OR为0.22(95%CI,0.17 - 0.26;P <.001)以及心血管死亡的OR为0.32(95%CI,0.25 - 0.40;P <.001)相关。
终生遗传暴露于较低水平的低密度脂蛋白胆固醇和较低的收缩压与较低的心血管风险相关。然而,不能假定这些发现代表通过治疗这些危险因素可实现的获益程度。