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Research Article| Volume 145, P6-11, March 2021

Depression and the Risk of Fractures in Later Life: the Health In Men Cohort Study

  • Osvaldo P. Almeida
    Correspondence
    Corresponding author at: WA Centre for Health & Ageing (M577), University of Western Australia, 35 Stirling Highway, Crawley, Perth, WA 6009, Australia.
    Affiliations
    Medical School, University of Western Australia, Perth, Australia

    WA Centre for Health and Ageing of the University of Western Australia, Perth, Australia
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  • Graeme J. Hankey
    Affiliations
    Medical School, University of Western Australia, Perth, Australia
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  • Jonathan Golledge
    Affiliations
    Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, Australia

    Department of Vascular and Endovascular Surgery, The Townsville Hospital, Townsville, Australia
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  • Bu B. Yeap
    Affiliations
    Medical School, University of Western Australia, Perth, Australia

    Department of Endocrinology and Diabetes, Fiona Stanley Hospital, Perth, Australia
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  • Leon Flicker
    Affiliations
    Medical School, University of Western Australia, Perth, Australia

    WA Centre for Health and Ageing of the University of Western Australia, Perth, Australia
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      Highlights

      • Depression has been associated with increased risk of fractures.
      • This longitudinal study confirmed that exposure to depression increases the risk of fractures, but the effect of this association is modest.
      • In this older cohort with multiple competing risks for fractures, exposure to antidepressant medications (including SSRIs) did not increase fracture risk.
      • The management of older adults with depression should include strategies for fracture prevention.

      Abstract

      Introduction

      Fractures are common and disabling health events, particularly later in life. The presence of clinically significant depressive symptoms has been associated with increased risk of fractures, and we designed the present study to clarify if this association is likely to be causal or due to the confounding effect of measures associated with both fractures and depression.

      Method

      Cohort study of a community-derived sample of 4224 men aged 70 to 88 years at the start of the follow-up period of up to 17 years. Clinically significant symptoms of depression were defined as a recorded diagnosis of depressive episode in the Western Australian Data Linkage System (WADLS) or by a total score of 7 or greater on the 15-item Geriatric Depression Scale. Health contacts associated with fractures were retrieved from WADLS. Other measures included age, past history of fractures, education, smoking, frailty, poor vision, falls, medications, and the concentration of vitamin D, homocysteine, hsCRP and testosterone. Death was considered a competing risk for fractures.

      Results

      911 (21.6%) participants had a bone fracture during follow-up. After adjustment for multiple potential confounders, past and current depression were associated with an increase in the risk of novel fractures; respective odds ratios were 1.41 (95%CI = 1.03, 1.93) and 1.64 (95%CI = 1.20, 2.25). Parsimonious competing risk regression showed that both past and current depression were associated with an increase in the risk of novel fractures: sub-hazard ratio = 1.29 (95%CI = 1.03, 1.63) and 1.27 (95%CI = 1.05, 1.55) respectively. Estimation of confounding due to unmeasured factors showed that a small additional effect could potentially dilute the association between depression and fractures.

      Discussion

      History of clinically significant symptoms of depression is associated with an increased risk of future fractures. This association may be due to multiple other associated risk factors, both measured and unmeasured, but nevertheless the presence of depression should alert clinicians to the need to develop a management plan that includes the management not only of depression but also of fracture risk.

      Keywords

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