Cardiovascular and mortality events in type 2 diabetes cardiovascular outcomes trials: a systematic review with trend analysis

被引:19
|
作者
Vetrone, Lorenzo M. [1 ,2 ]
Zaccardi, Francesco [1 ]
Webb, David R. [1 ]
Seidu, Sam [1 ]
Gholap, Nitin N. [3 ]
Pitocco, Dario [2 ]
Davies, Melanie J. [1 ]
Khunti, Kamlesh [1 ]
机构
[1] Leicester Gen Hosp, Diabet Res Ctr, Leicester Diabet Ctr, Gwendolen Rd, Leicester LE5 4PW, Leics, England
[2] Catholic Univ, Serv Diabetol, Sch Med, Largo Francesco Vito 1, I-00198 Rome, Italy
[3] Univ Hosp Coventry & Warwickshire, Clifford Bridge Rd, Coventry CV2 2DX, W Midlands, England
关键词
Cardiovascular; Type; 2; diabetes; Randomised trials; Mortality; Trend; Systematic review; HEART-FAILURE; ALL-CAUSE; MELLITUS; DISEASE; RATES; RISK; HYPOGLYCEMIA; INSULIN;
D O I
10.1007/s00592-018-1253-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsTo investigate cardiovascular disease and mortality trends in control arm participants of diabetes cardiovascular outcome trials (CVOTs).MethodsWe electronically searched CVOTs published before October 2017. Data on all-cause mortality, cardiovascular mortality and events, and baseline characteristics were collected, along with study calendar years. Trends were estimated using negative binomial regressions and reported as rate ratio (RR) per 5-year intervals.Results26 CVOTs, conducted from 1961 to 2015, included 86788 participants with 6543 all-cause deaths, 3265 cardiovascular deaths, and 7657 3-point major adverse cardiovascular events (3-P MACE; combined endpoint of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke). In unadjusted analysis, there was an increasing trend for 3-P MACE rates over time (5-year RR 1.57; 95% CI 1.34, 1.84); a small increasing trend for cardiovascular disease mortality rates (1.13; 1.01, 1.26); and stable rates for all-cause death. Adjusting for age, sex, previous myocardial infarction, and diabetes duration, there was no evidence of trends for 3-P MACE or cardiovascular disease mortality rates, while reducing rates were observed for nonfatal myocardial infarction (5-year RR: 0.72; 0.54, 0.96), total stroke (0.76; 0.66, 0.88), and nonfatal stroke (0.60; 0.43, 0.82).ConclusionsIn contrast to real-world data, there was no evidence of an improvement in all-cause and cardiovascular mortality in type 2 diabetes participants included in control arms of randomised clinical trials across 5 decades. Further studies should investigate whether and how dissimilarities in populations, procedures, and assessments of exposures and outcomes explain the differences between real-world setting and clinical trials.
引用
收藏
页码:331 / 339
页数:9
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