Sullivan Shannon D, Lehman Amy, Thomas Fridtjof, Johnson Karen C, Jackson Rebecca, Wactawski-Wende Jean, Ko Marcia, Chen Zhao, Curb J David, Howard Barbara V
1Division of Endocrinology and Metabolism, Department of Medicine, Medstar Washington Hospital Center, Washington, DC 2Center for Biostatistics, The Ohio State University, Columbus, OH 3Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN 4Department of Medicine, The Ohio State University, Columbus, OH 5Department of Social and Preventive Medicine, State University of New York, University at Buffalo, Buffalo, NY 6Department of Women's Health Internal Medicine, Mayo Clinic, Phoenix, AZ 7Department of Epidemiology and Biostatistics, Mel and Enid Zuckerman College of Public Health, University of Arizona, Tucson, AZ 8Department of Geriatric Medicine, University of Hawaii, Honolulu, HI 9Department of Medicine, Biostatistics, and Epidemiology, Medstar Health Research Institute, Hyattesville, MD.
Menopause. 2015 Oct;22(10):1035-44. doi: 10.1097/GME.0000000000000451.
Menopause is a risk factor for fracture; thus, menopause age may affect bone mass and fracture rates. We compared bone mineral density (BMD) and fracture rates among healthy postmenopausal women with varying ages at self-reported nonsurgical menopause.
We compared hazard ratios for fractures and differences in BMD among 21,711 postmenopausal women from the Women's Health Initiative Observational Study cohort who had no prior hysterectomy, oophorectomy, or hormone therapy and had varying self-reported ages at menopause (<40, 40-49, or ≥50 y).
Before multivariable adjustments, we found no differences in absolute fracture risk among menopause age groups. After multivariable adjustments for known risk factors for fracture, women who underwent menopause before age 40 years had a higher fracture risk at any site compared with women who underwent menopause at age 50 years or older (hazard ratio, 1.21; 95% CI, 1.02 to 1.44; P = 0.03). In a subset with BMD measurements (n = 1,351), whole-body BMD was lower in women who reported menopause before age 40 years than in women who reported menopause at ages 40 to 49 years (estimated difference, -0.034 g/cm; 95% CI, -0.07 to -0.004; P = 0.03) and women who reported menopause at age 50 years or older (estimated difference, -0.05 g/cm; 95% CI, -0.08 to -0.02; P < 0.01). Left hip BMD was lower in women who underwent menopause before age 40 years than in women who underwent menopause at age 50 years or older (estimated difference, -0.05 g/cm; 95% CI, -0.08 to -0.01; P = 0.01), and total spine BMD was lower in women who underwent menopause before age 40 years than in women who underwent menopause at age 50 years or older (estimated difference, -0.11 g/cm; 95% CI, -0.16 to -0.06; P < 0.01) and women who underwent menopause at ages 40 to 49 years (estimated difference, -0.09 g/cm; 95% CI, -0.15 to -0.04; P < 0.01).
In the absence of hormone therapy, younger age at menopause may be a risk factor contributing to decreased BMD and increased fracture risk in healthy postmenopausal women. Our data suggest that menopause age should be taken into consideration, along with other osteoporotic risk factors, when estimating fracture risk in postmenopausal women.
绝经是骨折的一个风险因素;因此,绝经年龄可能会影响骨量和骨折发生率。我们比较了自我报告非手术绝经年龄不同的健康绝经后女性的骨密度(BMD)和骨折发生率。
我们比较了来自女性健康倡议观察性研究队列的21711名绝经后女性的骨折风险比和BMD差异,这些女性既往未行子宫切除术、卵巢切除术或激素治疗,且自我报告的绝经年龄不同(<40岁、40 - 49岁或≥50岁)。
在多变量调整之前,我们发现绝经年龄组之间的绝对骨折风险没有差异。在对已知的骨折风险因素进行多变量调整后,40岁之前绝经的女性与50岁及以上绝经的女性相比,任何部位的骨折风险更高(风险比,1.21;95%置信区间,1.02至1.44;P = 0.03)。在有BMD测量值的亚组(n = 1351)中,报告40岁之前绝经的女性的全身BMD低于报告40至49岁绝经的女性(估计差异,-0.034 g/cm;95%置信区间,-0.07至-0.004;P = 0.03)以及报告50岁及以上绝经的女性(估计差异,-0.05 g/cm;95%置信区间,-0.08至-0.02;P < 0.01)。40岁之前绝经的女性的左髋BMD低于50岁及以上绝经的女性(估计差异,-0.05 g/cm;95%置信区间,-0.08至-0.01;P = 0.01),40岁之前绝经的女性的总脊柱BMD低于50岁及以上绝经的女性(估计差异,-0.ll g/cm;95%置信区间,-0.16至-0.06;P < 0.01)以及40至49岁绝经的女性(估计差异,-0.09 g/cm;95%置信区间,-0.15至-0.04;P < 0.01)。
在没有激素治疗的情况下,绝经年龄较小可能是导致健康绝经后女性BMD降低和骨折风险增加的一个风险因素。我们的数据表明,在评估绝经后女性的骨折风险时,应将绝经年龄与其他骨质疏松风险因素一并考虑。