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抑郁症与骨质疏松症:流行病学及潜在的中介途径。

Depression and osteoporosis: epidemiology and potential mediating pathways.

作者信息

Mezuk B, Eaton W W, Golden S H

机构信息

Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, 624 N. Broadway Suite 886, Baltimore, MD 21205, USA.

出版信息

Osteoporos Int. 2008 Jan;19(1):1-12. doi: 10.1007/s00198-007-0449-2. Epub 2007 Sep 1.

Abstract

INTRODUCTION

There have been numerous studies examining the association between depression and bone mineral density (BMD), but the underlying nature of this relationship remains unclear. Independent of this association, there is a growing body of evidence that depression impacts the risk for fracture in older adults. This article reviews the current epidemiological evidence regarding comorbidity of depression, low bone mineral density, and fracture.

METHODS

A review of the literature on depression, depressive symptoms, low BMD, osteoporosis, and fracture using electronic databases.

RESULTS

We reviewed 20 studies of the association between depression and BMD and five reports of the relationship between depression and fractures. Potential mediating mechanisms (both physiological and behavioral) are discussed, as well as potential confounding influences (e.g., medication use).

CONCLUSIONS

Most studies support the finding that depression is associated with increased risk for both low BMD and fractures, but variation in study design, sample composition, and exposure measurement make comparisons across studies difficult. Researchers should be aware of potential confounders, such as medication use, that may influence results. Future research should focus on identifying mediating pathways and targets for intervention in the relationships between depression, low BMD, and fracture.

摘要

引言

已有大量研究探讨抑郁症与骨密度(BMD)之间的关联,但这种关系的潜在本质仍不明确。独立于这种关联之外,越来越多的证据表明抑郁症会影响老年人骨折的风险。本文综述了有关抑郁症、低骨密度和骨折共病的当前流行病学证据。

方法

使用电子数据库对有关抑郁症、抑郁症状、低骨密度、骨质疏松症和骨折的文献进行综述。

结果

我们综述了20项关于抑郁症与骨密度关联的研究以及5篇关于抑郁症与骨折关系的报告。讨论了潜在的中介机制(包括生理和行为方面)以及潜在的混杂影响(例如药物使用)。

结论

大多数研究支持抑郁症与低骨密度和骨折风险增加相关这一发现,但研究设计、样本构成和暴露测量的差异使得跨研究比较变得困难。研究人员应意识到可能影响结果的潜在混杂因素,如药物使用。未来的研究应侧重于确定抑郁症、低骨密度和骨折之间关系的中介途径和干预靶点。

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