Sullivan Shannon D, Lehman Amy, Nathan Nisha K, Thomson Cynthia A, Howard Barbara V
1US Food and Drug Administration, Silver Spring, MD 2Center for Biostatistics, The Ohio State University, Columbus, OH 3Department of Medicine, Division of Endocrinology & Metabolism, George Washington University Medical Faculty Associates, Washington, DC 4Department of Health Promotion Sciences, Mel & Enid Zuckerman College of Public Health, University of Arizona, Tucson, AZ 5Medstar Health Research Institute and Georgetown/Howard Universities Center for Clinical and Translational Research, Hyattsville, MD.
Menopause. 2017 Apr;24(4):371-378. doi: 10.1097/GME.0000000000000775.
We previously reported that in the absence of hormone therapy (HT) or calcium/vitamin D (Ca/D) supplementation, earlier menopause age was associated with decreased bone mineral density and increased fracture risk in healthy postmenopausal women. Treatment with HT and Ca/D is protective against fractures after menopause. In this analysis, we asked if the age of menopause onset alters fracture risk in healthy postmenopausal women receiving HT, Ca/D, or a combination.
Hazard ratios (HRs) for any fracture among 21,711 healthy postmenopausal women enrolled in the Women's Health Initiative Clinical Trial, who were treated with HT, Ca/D, or HT + Ca/D, and who reported age of nonsurgical menopause of <40, 40 to 49, and ≥50 years, were compared.
Women with menopause <40 years had significantly higher HR for fracture than women with menopause 40 to 49 or ≥50 years, regardless of treatment intervention (HR [95% CI]: menopause <40 y vs ≥50 y, 1.36 [1.11-1.67]; menopause <40 y vs 40-49 y, 1.30 [1.06-1.60]).
In the overall Women's Health Initiative Clinical Trial cohort and within each treatment group, women with younger menopause age (<40 y) had a higher risk of any fracture than women reporting older menopause ages. The effect of menopause age on fracture risk was not altered by any of the treatment interventions (HT, Ca/D, HT + Ca/D), suggesting that early age of menopause is an independent contributor to postmenopausal fracture risk.
我们之前报道过,在未进行激素治疗(HT)或补充钙/维生素D(Ca/D)的情况下,较早的绝经年龄与健康绝经后女性骨密度降低及骨折风险增加相关。HT和Ca/D治疗可预防绝经后骨折。在本分析中,我们探讨了绝经起始年龄是否会改变接受HT、Ca/D或两者联合治疗的健康绝经后女性的骨折风险。
比较了参加女性健康倡议临床试验的21711名健康绝经后女性中,接受HT、Ca/D或HT + Ca/D治疗且报告非手术绝经年龄<40岁、40至49岁和≥50岁的女性发生任何骨折的风险比(HRs)。
无论治疗干预如何,绝经年龄<40岁的女性骨折的HR显著高于绝经年龄为40至49岁或≥50岁的女性(HR [95% CI]:绝经<40岁与≥50岁相比,1.36 [1.11 - 1.67];绝经<40岁与40 - 49岁相比,1.30 [1.06 - 1.60])。
在整个女性健康倡议临床试验队列以及每个治疗组中,绝经年龄较小(<40岁)的女性发生任何骨折的风险高于绝经年龄较大的女性。绝经年龄对骨折风险的影响未因任何治疗干预(HT、Ca/D、HT + Ca/D)而改变,这表明绝经年龄较早是绝经后骨折风险的一个独立因素。