Svensson Thomas, Kitlinski Mariusz, Engström Gunnar, Melander Olle
Department of Clinical Sciences, Lund University, Malmö, Sweden.
Department of Global Health Policy, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo Japan.
PLoS One. 2017 Apr 20;12(4):e0176029. doi: 10.1371/journal.pone.0176029. eCollection 2017.
Psychological stress is an independent risk factor for cardiovascular disease (CVD), but the mechanism by which stress is associated with CVD is not entirely understood. Although genetic factors are implied in both stress responsivity and cardiovascular reactivity, no studies to date have investigated their interactions with stress for cardiovascular end points. The objective was to elucidate the association and interactions between a genetic risk score (GRS), individual genetic variants and stress for three cardiovascular end points: coronary artery disease (CAD), fatal myocardial infarction (MI), non-fatal MI, and cardiovascular death.
18,559 participants from the Malmö Diet Cancer Study, a population-based prospective study, were included in the analyses. Cox proportional hazards regression models were used and adjusted for a large number of known predictors of cardiovascular end points. Mean follow-up time in years was 14.6 (CAD; n = 1938), 14.8 (fatal MI; n = 436), 14.8 (non-fatal MI; n = 1108), and 15.1 (cardiovascular death; n = 1071) respectively. GRS was significantly associated with increased risks of CAD (top quartile hazard ratio [HR], 1.72; 95% confidence interval [CI], 1.51-1.96), fatal MI (top quartile HR, 1.62; 95%CI, 1.23-2.15), non-fatal MI (top quartile HR, 1.55; 95%CI, 1.31-1.84), and cardiovascular death (top quartile HR, 1.29; 95%CI, 1.08-1.53). Stress was not independently associated with any end point and did not interact with GRS. Four individual genetic variants interacted unfavorably with stress for end points with mortality outcomes.
A GRS composed of 50 SNPs and predictive of CAD was found for the first time to also strongly predict fatal MI, non-fatal MI and cardiovascular death. A stress-sensitive component of the GRS was isolated on the basis of individual genetic variants that interacted unfavorably with stress.
心理压力是心血管疾病(CVD)的独立危险因素,但压力与心血管疾病相关的机制尚未完全明确。尽管遗传因素在压力反应性和心血管反应性中均有体现,但迄今为止尚无研究调查它们与压力对心血管终点的相互作用。目的是阐明遗传风险评分(GRS)、个体基因变异与压力之间对于三个心血管终点的关联及相互作用,这三个终点分别为冠状动脉疾病(CAD)、致命性心肌梗死(MI)、非致命性MI以及心血管死亡。
纳入了来自马尔默饮食与癌症研究(一项基于人群的前瞻性研究)的18559名参与者进行分析。使用Cox比例风险回归模型,并针对大量已知的心血管终点预测因素进行了调整。以年为单位的平均随访时间分别为14.6年(CAD;n = 1938)、14.8年(致命性MI;n = 436)、14.8年(非致命性MI;n = 1108)以及15.1年(心血管死亡;n = 1071)。GRS与CAD风险增加显著相关(最高四分位数风险比[HR],1.72;95%置信区间[CI],1.51 - 1.96)、致命性MI(最高四分位数HR,1.62;95%CI,1.23 - 2.15)、非致命性MI(最高四分位数HR,1.55;95%CI,1.31 - 1.84)以及心血管死亡(最高四分位数HR,1.29;95%CI,1.08 - 1.53)。压力与任何终点均无独立关联,且与GRS无相互作用。四个个体基因变异与压力对具有死亡结局的终点产生了不利的相互作用。
首次发现由50个单核苷酸多态性(SNP)组成且可预测CAD的GRS也能强烈预测致命性MI、非致命性MI和心血管死亡。基于与压力产生不利相互作用的个体基因变异,分离出了GRS中的一个压力敏感成分。