Prentice Ross L, Pettinger Mary, Anderson Garnet L
Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.
Biometrics. 2005 Dec;61(4):899-911; discussion 911-41. doi: 10.1111/j.0006-341X.2005.454_1.x.
A brief overview of the design of the Women's Health Initiative (WHI) clinical trial and observational study is provided along with a summary of results from the postmenopausal hormone therapy clinical trial components. Since its inception in 1992, the WHI has encountered a number of statistical issues where further methodology developments are needed. These include measurement error modeling and analysis procedures for dietary and physical activity assessment; clinical trial monitoring methods when treatments may affect multiple clinical outcomes, either beneficially or adversely; study design and analysis procedures for high-dimensional genomic and proteomic data; and failure time data analysis procedures when treatment group hazard ratios are time dependent. This final topic seems important in resolving the discrepancy between WHI clinical trial and observational study results on postmenopausal hormone therapy and cardiovascular disease.
本文简要概述了妇女健康倡议(WHI)临床试验和观察性研究的设计,并总结了绝经后激素治疗临床试验部分的结果。自1992年启动以来,WHI遇到了一些需要进一步发展方法学的统计问题。这些问题包括饮食和身体活动评估的测量误差建模与分析程序;当治疗可能对多种临床结局产生有益或不利影响时的临床试验监测方法;高维基因组和蛋白质组数据的研究设计与分析程序;以及当治疗组风险比随时间变化时的生存时间数据分析程序。最后一个主题在解决WHI临床试验与绝经后激素治疗及心血管疾病观察性研究结果之间的差异方面似乎很重要。