Ardern Chris I, Katzmarzyk Peter T, Janssen Ian, Church Timothy S, Blair Steven N
School of Physical and Health Education, Queen's University, Kingston, Ontario, K7L 3N6, Canada.
Circulation. 2005 Sep 6;112(10):1478-85. doi: 10.1161/CIRCULATIONAHA.105.548198. Epub 2005 Aug 29.
National Cholesterol Education Program Adult Treatment Panel III guidelines recommend therapeutic lifestyle changes (TLC) and drug therapy to reduce cardiovascular disease (CVD) risk. These guidelines have been revised recently (ATP III-R); however, the risk of CVD mortality within each intervention window and the effects of cardiorespiratory fitness (CRF) and metabolic syndrome on CVD mortality within the framework of the guidelines are unknown.
Risk factor and CRF data from 19,125 men (aged 20 to 79 years) who attended a preventive medical clinic between 1979 and 1995 were used. Mortality follow-up was completed until December 31, 1996. Participants were assigned to ATP III-R groups (LDL-C goal, TLC initiation, and drug consideration), and risk of CVD mortality was assessed by Cox proportional hazards regression. There were 179 CVD deaths over an average 10.2 years of follow-up. Compared with the LDL-C goal group, men in the TLC initiation and drug consideration groups had an elevated risk of CVD mortality (TLC initiation: HR=2.65, 95% CI 1.67 to 4.19; drug consideration: HR=6.44, 95% CI 4.49 to 9.25). Compared with LDL-C goal/fit, CVD mortality risk was higher in the LDL-C goal/unfit (4.8, 2.5 to 9.1), TLC initiation/fit (3.0, 1.7 to 5.3), TLC initiation/unfit (7.5, 3.7 to 15.2), drug consideration/fit (7.2, 4.6 to 11.4), and drug consideration/unfit (14.9, 9.1 to 24.4) groups. A similar gradient was observed for metabolic syndrome across intervention windows.
Men eligible for TLC or drug consideration under ATP III-R were at elevated risk of CVD mortality compared with men who met the LDL-C goal. Furthermore, men who were physically fit or who did not have the metabolic syndrome had a lower risk of CVD mortality.
美国国家胆固醇教育计划成人治疗专家组第三次报告(ATP III)指南推荐采用治疗性生活方式改变(TLC)和药物治疗来降低心血管疾病(CVD)风险。这些指南最近已修订(ATP III-R);然而,在每个干预阶段内心血管疾病死亡风险以及在该指南框架中心肺适能(CRF)和代谢综合征对心血管疾病死亡的影响尚不清楚。
使用了1979年至1995年间在一家预防医学诊所就诊的19125名男性(年龄在20至79岁之间)的危险因素和心肺适能数据。死亡随访至1996年12月31日结束。参与者被分配到ATP III-R组(低密度脂蛋白胆固醇目标、开始TLC和考虑药物治疗),并通过Cox比例风险回归评估心血管疾病死亡风险。在平均10.2年的随访期间有179例心血管疾病死亡。与低密度脂蛋白胆固醇目标组相比,开始TLC组和考虑药物治疗组的男性心血管疾病死亡风险升高(开始TLC:风险比=2.65,95%置信区间1.67至4.19;考虑药物治疗:风险比=6.44,95%置信区间4.49至9.25)。与低密度脂蛋白胆固醇目标/健康组相比,低密度脂蛋白胆固醇目标/不健康组(4.8,2.5至9.1)、开始TLC/健康组(3.0,1.7至5.3)、开始TLC/不健康组(7.5,3.7至15.2)、考虑药物治疗/健康组(7.2,4.6至11.4)和考虑药物治疗/不健康组(14.9,9.1至24.4)的心血管疾病死亡风险更高。在各干预阶段观察到代谢综合征有类似的梯度变化。
与达到低密度脂蛋白胆固醇目标的男性相比,符合ATP III-R中TLC或药物治疗条件的男性心血管疾病死亡风险升高。此外,身体健康或没有代谢综合征的男性心血管疾病死亡风险较低。