Shumaker Sally A, Legault Claudine, Kuller Lewis, Rapp Stephen R, Thal Leon, Lane Dorothy S, Fillit Howard, Stefanick Marcia L, Hendrix Susan L, Lewis Cora E, Masaki Kamal, Coker Laura H
Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
JAMA. 2004 Jun 23;291(24):2947-58. doi: 10.1001/jama.291.24.2947.
The Women's Health Initiative Memory Study (WHIMS) previously found increased risk for dementia and no effect on mild cognitive impairment (MCI) in women treated with conjugated equine estrogens (CEE) plus medroxyprogesterone acetate (MPA).
To determine the effects of CEE alone and CEE plus MPA on incidence of probable dementia and MCI in older women.
DESIGN, SETTING, AND PARTICIPANTS: Randomized, double-blind, placebo-controlled clinical trials of CEE (estrogen-alone trial) or CEE plus MPA (estrogen plus progestin trial) in community-dwelling women aged 65 to 79 years, conducted from June 1995 to July 8, 2002 (estrogen plus progestin; n = 4532), or to February 29, 2004 (estrogen-alone; n = 2947), in 39 of the 40 WHI clinical centers.
In the estrogen-alone trial, 1 daily tablet containing either 0.625 mg/d of CEE vs matching placebo; in the estrogen plus progestin trial, 1 daily tablet containing CEE (0.625 mg/d) plus MPA (2.5 mg/d) vs matching placebos.
Probable dementia and MCI.
In the estrogen-alone trial, 47 participants were diagnosed with probable dementia, of whom 28 were assigned to CEE and 19 to placebo (hazard ratio [HR], 1.49; 95% confidence interval [CI], 0.83-2.66). Incidence rates for probable dementia in the estrogen-alone trial were statistically similar to those in the estrogen plus progestin trial (45 vs 22 per 10 000 person-years for CEE plus MPA vs placebo, respectively; P =.11). When data were pooled per the original WHIMS protocol, the overall HR for probable dementia was 1.76 (95% CI, 1.19-2.60; P =.005). After excluding participants with baseline Modified Mini-Mental State Examination scores at or below the screening cut point, the HR was 1.77 (95% CI, 0.74-4.23; P =.20) in the estrogen-alone trial and 2.19 (95% CI, 1.25-3.84; P =.006) in the pooled trials. In the estrogen-alone trial, 76 participants were diagnosed with MCI in the CEE group vs 58 in the placebo group (HR, 1.34; 95% CI, 0.95-1.89). In the combined trial data, the HR was similar (1.25; 95% CI, 0.97-1.60). In the estrogen-alone trial, 93 participants receiving CEE were diagnosed with either probable dementia or MCI vs 69 receiving placebo (HR, 1.38; 95% CI, 1.01-1.89; P =.04).
Estrogen therapy alone did not reduce dementia or MCI incidence and increased the risk for both end points combined. Pooling data for estrogen alone and estrogen plus progestin resulted in increased risks for both end points. Use of hormone therapy to prevent dementia or cognitive decline in women 65 years of age or older is not recommended.
妇女健康倡议记忆研究(WHIMS)先前发现,接受结合马雌激素(CEE)加醋酸甲羟孕酮(MPA)治疗的女性患痴呆症的风险增加,而对轻度认知障碍(MCI)无影响。
确定单独使用CEE以及CEE加MPA对老年女性可能患痴呆症和MCI发生率的影响。
设计、地点和参与者:1995年6月至2002年7月8日(雌激素加孕激素组;n = 4532)或至2004年2月29日(单独使用雌激素组;n = 2947)在40个WHI临床中心中的39个中心,对65至79岁社区居住女性进行的CEE(单独使用雌激素试验)或CEE加MPA(雌激素加孕激素试验)的随机、双盲、安慰剂对照临床试验。
在单独使用雌激素试验中,每日服用1片含0.625 mg/d CEE的片剂或匹配的安慰剂;在雌激素加孕激素试验中,每日服用1片含CEE(0.625 mg/d)加MPA(2.5 mg/d)的片剂或匹配的安慰剂。
可能患痴呆症和MCI。
在单独使用雌激素试验中,47名参与者被诊断为可能患痴呆症,其中28名被分配到CEE组,19名被分配到安慰剂组(风险比[HR],1.49;95%置信区间[CI],0.83 - 2.66)。单独使用雌激素试验中可能患痴呆症的发生率与雌激素加孕激素试验中的发生率在统计学上相似(CEE加MPA组与安慰剂组分别为每10000人年45例与22例;P = 0.11)。按照原始WHIMS方案汇总数据时,可能患痴呆症的总体HR为1.76(95%CI,1.19 - 2.60;P = 0.005)。排除基线改良简易精神状态检查评分处于或低于筛查切点水平的参与者后,单独使用雌激素试验中的HR为1.77(95%CI,0.74 - 4.23;P = 0.20),汇总试验中的HR为2.19(95%CI,1.25 - 3.84;P = 0.006)。在单独使用雌激素试验中,CEE组有76名参与者被诊断为MCI,安慰剂组有58名(HR,1.34;95%CI,0.95 - 1.89)。在合并试验数据中,HR相似(1.25;95%CI,0.97 - 1.60)。在单独使用雌激素试验中,接受CEE治疗的93名参与者被诊断为可能患痴呆症或MCI,接受安慰剂治疗的有69名(HR,1.38;95%CI,1.01 - 1.89;P = 0.04)。
单独使用雌激素疗法不能降低痴呆症或MCI的发生率,且增加了两者合并的风险。汇总单独使用雌激素和雌激素加孕激素的数据会增加两个终点的风险。不建议使用激素疗法预防65岁及以上女性的痴呆症或认知衰退。