Chen Qian, Zhang Yuan, Ding Ding, Li Dan, Xia Min, Li Xinrui, Yang Yunou, Li Qing, Hu Gang, Ling Wenhua
Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Department of Nutrition, School of Public Health, Sun Yat-sen University, No. 74 Zhongshan Road 2, Guangzhou, Guangdong 510080, China; Chronic Disease Epidemiology Laboratory, Pennington Biomedical Research Center, 6400 Perkins Road, Baton Rouge, LA 70808, USA.
Department of Cardiology, General Hospital of Guangzhou Military Command of People's Liberation Army, Guangdong 510010, China.
Int J Cardiol. 2016 Dec 1;224:8-14. doi: 10.1016/j.ijcard.2016.08.324. Epub 2016 Aug 22.
The metabolic syndrome (MetS) and its metabolic risk factors appear to promote the development of atherosclerotic cardiovascular disease. The aim of this study was to examine the association of MetS and its individual components with all-cause and cardiovascular mortality among patients with coronary heart disease (CHD).
We performed a prospective, hospital-based cohort among 3599 CHD patients in China. Cox proportional hazards regression models were used to estimate the association of MetS and its components at baseline with risk of mortality.
During a mean follow-up period of 4.9years, 308 deaths were identified, 200 of which were due to cardiovascular disease. Compared with patients without MetS, patients with MetS according to the AHA/NHLBI statement had a 1.26-fold higher risk (95% CI, 1.01-1.59) of all-cause mortality and a 1.41-fold higher risk (1.06-1.87) of cardiovascular mortality. Patients with increasing numbers of components of MetS had a gradually increased risk for all-cause and cardiovascular mortality (P<0.05). When each component of MetS was considered as a dichotomized variable separately, only low high-density lipoprotein cholesterol (HDL-C) and elevated fasting blood glucose (FBG) were associated with all-cause and cardiovascular mortality. After using restricted cubic splines, we found a U-shaped association of HDL-C, body mass index and blood pressure, a positive association of FBG, and no association of triglycerides with the risks of all-cause and cardiovascular mortality.
MetS is a risk factor for all-cause and cardiovascular mortality among CHD patients. It is very important to control metabolic components in a reasonable control range.
代谢综合征(MetS)及其代谢危险因素似乎会促进动脉粥样硬化性心血管疾病的发展。本研究的目的是探讨MetS及其各个组成部分与冠心病(CHD)患者全因死亡率和心血管死亡率之间的关联。
我们在中国的3599例CHD患者中进行了一项基于医院的前瞻性队列研究。采用Cox比例风险回归模型来估计基线时MetS及其组成部分与死亡风险之间的关联。
在平均4.9年的随访期内,共确定了308例死亡病例,其中200例死于心血管疾病。与无MetS的患者相比,根据美国心脏协会/美国国立心肺血液研究所(AHA/NHLBI)声明诊断为MetS的患者全因死亡风险高1.26倍(95%置信区间[CI],1.01 - 1.59),心血管死亡风险高1.41倍(1.06 - 1.87)。MetS组成部分数量增加的患者全因和心血管死亡风险逐渐增加(P<0.05)。当将MetS的每个组成部分分别作为二分变量考虑时,只有低高密度脂蛋白胆固醇(HDL-C)和空腹血糖(FBG)升高与全因和心血管死亡率相关。使用受限立方样条分析后,我们发现HDL-C、体重指数和血压呈U形关联,FBG呈正相关,甘油三酯与全因和心血管死亡风险无关联。
MetS是CHD患者全因和心血管死亡的危险因素。将代谢成分控制在合理范围内非常重要。