Guthrie Katherine A, LaCroix Andrea Z, Ensrud Kristine E, Joffe Hadine, Newton Katherine M, Reed Susan D, Caan Bette, Carpenter Janet S, Cohen Lee S, Freeman Ellen W, Larson Joseph C, Manson JoAnn E, Rexrode Kathy, Skaar Todd C, Sternfeld Barbara, Anderson Garnet L
MsFLASH Data Coordinating Center, Fred Hutchinson Cancer Research Center, the Group Health Research Institute, and the University of Washington School of Medicine, Seattle, Washington; the Department of Family and Preventive Medicine, University of California, San Diego, San Diego, and the Division of Research, Kaiser Permanente, Oakland, California; the VA Medical Center/University of Minnesota, Minneapolis, Minnesota; Brigham and Women's Hospital, Dana Farber Cancer Institute, and Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts; the School of Nursing and the Department of Medicine, Division of Clinical Pharmacology, Indiana University, Indianapolis, Indiana; and the Departments of Obstetrics and Gynecology and Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania.
Obstet Gynecol. 2015 Aug;126(2):413-422. doi: 10.1097/AOG.0000000000000927.
To describe the effects of six interventions for menopausal vasomotor symptoms relative to control in a pooled analysis, facilitating translation of the results for clinicians and symptomatic women. The Menopause Strategies: Finding Lasting Answers for Symptoms and Health network tested these interventions in three randomized clinical trials.
An analysis of pooled individual-level data from three randomized clinical trials is presented. Participants were 899 perimenopausal and postmenopausal women with at least 14 bothersome vasomotor symptoms per week. Interventions included 10-20 mg escitalopram per day, nonaerobic yoga, aerobic exercise, 1.8 g per day omega-3 fatty acid supplementation, 0.5 mg low-dose oral 17-beta-estradiol (E2) per day, and 75 mg low-dose venlafaxine XR per day. The main outcome measures were changes from baseline in mean daily vasomotor symptom frequency and bother during 8-12 weeks of treatment. Linear regression models estimated differences in outcomes between each intervention and corresponding control group adjusted for baseline characteristics. Models included trial-specific intercepts, effects of the baseline outcome measure, and time.
The 8-week reduction in vasomotor symptom frequency from baseline relative to placebo was similar for escitalopram at -1.4 per day (95% confidence interval [CI] -2.7 to -0.2), low-dose E2 at -2.4 (95% CI -3.4 to -1.3), and venlafaxine at -1.8 (95% CI -2.8 to -0.8); vasomotor symptom bother reduction was minimal and did not vary across these three pharmacologic interventions (mean -0.2 to -0.3 relative to placebo). No effects on vasomotor symptom frequency or bother were seen with aerobic exercise, yoga, or omega-3 supplements.
These analyses suggest that escitalopram, low-dose E2, and venlafaxine provide comparable, modest reductions in vasomotor symptom frequency and bother among women with moderate hot flushes.
ClinicalTrials.gov, www.clinicaltrials.gov, NCT00894543 (MsFLASH 01), NCT01178892 (MsFLASH 02), and NCT01418209 (MsFLASH 03).
在一项汇总分析中描述六种针对绝经后血管舒缩症状的干预措施相对于对照的效果,以便为临床医生和有症状的女性转化研究结果。绝经策略:寻找症状与健康的持久答案网络在三项随机临床试验中对这些干预措施进行了测试。
呈现了对三项随机临床试验中个体水平汇总数据的分析。参与者为899名围绝经期和绝经后女性,每周至少有14次令人烦恼的血管舒缩症状。干预措施包括每天10 - 20毫克艾司西酞普兰、非有氧运动瑜伽、有氧运动、每天补充1.8克ω-3脂肪酸、每天0.5毫克低剂量口服17-β-雌二醇(E2)以及每天75毫克低剂量文拉法辛缓释片。主要结局指标为治疗8 - 12周期间每日血管舒缩症状频率和困扰程度相对于基线的变化。线性回归模型估计了每种干预措施与相应对照组在调整基线特征后的结局差异。模型包括特定试验的截距、基线结局指标的效应和时间。
与安慰剂相比,艾司西酞普兰使血管舒缩症状频率从基线水平在8周时每日减少1.4次(95%置信区间[CI] -2.7至 -0.2),低剂量E2为减少2.4次(95% CI -3.4至 -1.3),文拉法辛为减少1.8次(95% CI -2.8至 -0.8),三者相似;在这三种药物干预措施中,血管舒缩症状困扰程度的降低最小且无差异(相对于安慰剂平均降低 -0.2至 -0.3)。有氧运动、瑜伽或ω-3补充剂对血管舒缩症状频率或困扰程度均无影响。
这些分析表明,艾司西酞普兰、低剂量E2和文拉法辛在中度潮热女性中可使血管舒缩症状频率和困扰程度得到相当程度的适度降低。
ClinicalTrials.gov,www.clinicaltrials.gov,NCT00894543(MsFLASH 01)、NCT01178892(MsFLASH 02)和NCT01418209(MsFLASH