Lonn Eva, Bosch Jackie, Yusuf Salim, Sheridan Patrick, Pogue Janice, Arnold J Malcolm O, Ross Catherine, Arnold Andrew, Sleight Peter, Probstfield Jeffrey, Dagenais Gilles R
Population Health Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, Ontario.
JAMA. 2005 Mar 16;293(11):1338-47. doi: 10.1001/jama.293.11.1338.
Experimental and epidemiological data suggest that vitamin E supplementation may prevent cancer and cardiovascular events. Clinical trials have generally failed to confirm benefits, possibly due to their relatively short duration.
To evaluate whether long-term supplementation with vitamin E decreases the risk of cancer, cancer death, and major cardiovascular events.
DESIGN, SETTING, AND PATIENTS: A randomized, double-blind, placebo-controlled international trial (the initial Heart Outcomes Prevention Evaluation [HOPE] trial conducted between December 21, 1993, and April 15, 1999) of patients at least 55 years old with vascular disease or diabetes mellitus was extended (HOPE-The Ongoing Outcomes [HOPE-TOO]) between April 16, 1999, and May 26, 2003. Of the initial 267 HOPE centers that had enrolled 9541 patients, 174 centers participated in the HOPE-TOO trial. Of 7030 patients enrolled at these centers, 916 were deceased at the beginning of the extension, 1382 refused participation, 3994 continued to take the study intervention, and 738 agreed to passive follow-up. Median duration of follow-up was 7.0 years.
Daily dose of natural source vitamin E (400 IU) or matching placebo.
Primary outcomes included cancer incidence, cancer deaths, and major cardiovascular events (myocardial infarction, stroke, and cardiovascular death). Secondary outcomes included heart failure, unstable angina, and revascularizations.
Among all HOPE patients, there were no significant differences in the primary analysis: for cancer incidence, there were 552 patients (11.6%) in the vitamin E group vs 586 (12.3%) in the placebo group (relative risk [RR], 0.94; 95% confidence interval [CI], 0.84-1.06; P = .30); for cancer deaths, 156 (3.3%) vs 178 (3.7%), respectively (RR, 0.88; 95% CI, 0.71-1.09; P = .24); and for major cardiovascular events, 1022 (21.5%) vs 985 (20.6%), respectively (RR, 1.04; 95% CI, 0.96-1.14; P = .34). Patients in the vitamin E group had a higher risk of heart failure (RR, 1.13; 95% CI, 1.01-1.26; P = .03) and hospitalization for heart failure (RR, 1.21; 95% CI, 1.00-1.47; P = .045). Similarly, among patients enrolled at the centers participating in the HOPE-TOO trial, there were no differences in cancer incidence, cancer deaths, and major cardiovascular events, but higher rates of heart failure and hospitalizations for heart failure.
In patients with vascular disease or diabetes mellitus, long-term vitamin E supplementation does not prevent cancer or major cardiovascular events and may increase the risk for heart failure.
实验和流行病学数据表明,补充维生素E可能预防癌症和心血管事件。临床试验通常未能证实其益处,这可能是由于试验持续时间相对较短。
评估长期补充维生素E是否能降低癌症、癌症死亡及主要心血管事件的风险。
设计、地点和患者:一项随机、双盲、安慰剂对照的国际试验(最初的心脏结局预防评估[HOPE]试验于1993年12月21日至1999年4月15日进行),针对至少55岁的血管疾病或糖尿病患者,该试验于1999年4月16日至2003年5月26日进行了扩展(HOPE-持续结局[HOPE-TOO])。最初参与招募9541名患者的267个HOPE中心中,有174个中心参与了HOPE-TOO试验。在这些中心招募的7030名患者中,916名在扩展期开始时已死亡,1382名拒绝参与,3994名继续接受研究干预,738名同意被动随访。中位随访时间为7.0年。
每日服用天然来源的维生素E(400国际单位)或匹配的安慰剂。
主要结局包括癌症发病率、癌症死亡及主要心血管事件(心肌梗死、中风和心血管死亡)。次要结局包括心力衰竭、不稳定型心绞痛和血管重建术。
在所有HOPE患者中,初步分析无显著差异:癌症发病率方面,维生素E组有552名患者(11.6%),安慰剂组有586名患者(12.3%)(相对风险[RR],0.94;95%置信区间[CI],0.84 - 1.06;P = 0.30);癌症死亡方面,分别为156名(3.3%)和178名(3.7%)(RR,0.88;95% CI,0.71 - 1.09;P = 0.24);主要心血管事件方面,分别为1022名(21.5%)和985名(20.6%)(RR,1.04;95% CI,0.96 - 1.14;P = 0.34)。维生素E组患者发生心力衰竭的风险更高(RR,1.13;95% CI,1.01 - 1.26;P = 0.03),因心力衰竭住院的风险也更高(RR,1.21;95% CI,1.00 - 1.47;P = 0.045)。同样,在参与HOPE-TOO试验中心招募的患者中,癌症发病率、癌症死亡及主要心血管事件方面无差异,但心力衰竭及因心力衰竭住院的发生率更高。
在血管疾病或糖尿病患者中,长期补充维生素E不能预防癌症或主要心血管事件,且可能增加心力衰竭风险。