Spangler Leslie, Scholes Delia, Brunner Robert L, Robbins John, Reed Susan D, Newton Katherine M, Melville Jennifer L, Lacroix Andrea Z
Group Health Center for Health Studies, Seattle, WA, USA.
J Gen Intern Med. 2008 May;23(5):567-74. doi: 10.1007/s11606-008-0525-0. Epub 2008 Feb 20.
Osteoporosis and depression may be associated through common physiologic systems or risk factors.
To assess the associations between depressive symptoms (Burnam's scale) or antidepressant use and bone outcomes.
Prospective cohort study.
A total of 93,676 postmenopausal women (50 to 79 years old) enrolled in the Women's Health Initiative Observational Study.
Self-reported fractures (n = 14,982) (hip [adjudicated], spine, wrist, and "other"). Analyses included 82,410 women with complete information followed on average for 7.4 years. Bone mineral density (BMD) of the hip (n = 4539), spine (n = 4417), and whole body (n = 4502) was measured at baseline and 3 years in women enrolled at 3 densitometry study sites.
Overall, there were no statistically significant associations between depressive symptoms or antidepressant therapy and 3-year change in BMD. In a subset of women not using antidepressants, there was a significant difference in whole-body BMD change between women with and without depressive symptoms (P = .05). Depressive symptoms (hazard ratio [HR] 1.08; 95% CI = 1.02 to 1.14) and antidepressant therapy (HR = 1.22; CI = 1.15 to 1.30) independently increased risk of any fracture, the majority of which occurred at "other" anatomic sites. Antidepressant therapy increased the risk of spine fracture (HR = 1.36; CI = 1.14 to 1.63). No associations were observed between depressive symptoms or antidepressant therapy and hip or wrist fracture.
In this study of postmenopausal women, average age 64, we observed minimal association between depressive symptoms and 3-year changes in either BMD or fracture risk. Antidepressant use was not associated with changes in BMD, but was associated with increased risk of fractures at the spine and "other " anatomic sites.
骨质疏松症与抑郁症可能通过共同的生理系统或风险因素相互关联。
评估抑郁症状(伯纳姆量表)或抗抑郁药物使用与骨骼结局之间的关联。
前瞻性队列研究。
共有93676名绝经后女性(年龄在50至79岁之间)参与了女性健康倡议观察性研究。
自我报告的骨折情况(n = 14982)(髋部[经判定]、脊柱、腕部和“其他”)。分析纳入了82410名信息完整的女性,她们平均随访了7.4年。在3个骨密度研究地点入组的女性中,于基线和3年时测量了髋部(n = 4539)、脊柱(n = 4417)和全身(n = 4502)的骨密度。
总体而言,抑郁症状或抗抑郁治疗与骨密度的3年变化之间无统计学显著关联。在未使用抗抑郁药物的女性亚组中,有抑郁症状和无抑郁症状的女性在全身骨密度变化方面存在显著差异(P = 0.05)。抑郁症状(风险比[HR] 1.08;95%置信区间[CI] = 1.02至1.14)和抗抑郁治疗(HR = 1.22;CI = 1.15至1.30)均独立增加了任何骨折的风险,其中大多数骨折发生在“其他”解剖部位。抗抑郁治疗增加了脊柱骨折的风险(HR = 1.36;CI = 1.14至1.63)。未观察到抑郁症状或抗抑郁治疗与髋部或腕部骨折之间存在关联。
在这项针对平均年龄为64岁的绝经后女性的研究中,我们观察到抑郁症状与骨密度或骨折风险的3年变化之间关联极小。抗抑郁药物的使用与骨密度变化无关,但与脊柱和“其他”解剖部位骨折风险增加有关。