TY - JOUR
T1 - Association between bone mineral density and depressive symptoms in a population-based sample
AU - Hlis, Rocco D.
AU - McIntyre, Roger S.
AU - Maalouf, Naim M.
AU - Van Enkevort, Erin
AU - Brown, E. Sherwood
N1 - Publisher Copyright:
© Copyright 2017 Physicians Postgraduate Press, Inc.
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Objective: This analysis was conducted to determine the relationship between bone mineral density (BMD) and depressive symptoms in a population-based cohort. Methods: Data were extracted from the second phase of the Dallas Heart Study (DHS-2), a large, multiethnic population sample in Dallas County, Texas, from September 1, 2007, to December 31, 2009. Depressive symptom severity was measured with the 16-item Quick Inventory of Depressive Symptomatology - Self Report (QIDS-S16), which is derived from DSM-IV major depressive disorder criteria. BMD was measured using dual-energy x-ray absorptiometry. Multiple linear regressions examined the relationship between QIDS-S16 score and BMD controlling for age, body mass index, sex, ethnicity, smoking status, alcohol use status, serum 25-hydroxyvitamin D concentration, antidepressant use, and physical activity as measured by total vigorous and moderate metabolic equivalents. Subgroup analyses explored differences related to age. Results: QIDS-SR16 score was not a significant predictor of either lumbar spine or total hip T-score (β = -0.01, P = .61 and β = -0.02, P = .39) in the overall population (n = 2,285). There was a significant negative interaction term between age and QIDS-S16 group (β = -0.01, P = .01). In participants aged 60 years or older (n = 465), QIDS-S16 score was a significant predictor of BMD at the lumbar spine and total hip (β = -0.14, P = .003 and β = -0.12, P = .006, respectively). Conclusions: QIDS-S16 score did not significantly predict BMD in the overall DHS-2 sample. There was, however, a significant association observed in participants aged ≤ 60 years. Results suggest that diagnosis and treatment of depressive symptoms may be of clinical importance in older individuals, a subgroup at high risk for osteoporosis and fractures.
AB - Objective: This analysis was conducted to determine the relationship between bone mineral density (BMD) and depressive symptoms in a population-based cohort. Methods: Data were extracted from the second phase of the Dallas Heart Study (DHS-2), a large, multiethnic population sample in Dallas County, Texas, from September 1, 2007, to December 31, 2009. Depressive symptom severity was measured with the 16-item Quick Inventory of Depressive Symptomatology - Self Report (QIDS-S16), which is derived from DSM-IV major depressive disorder criteria. BMD was measured using dual-energy x-ray absorptiometry. Multiple linear regressions examined the relationship between QIDS-S16 score and BMD controlling for age, body mass index, sex, ethnicity, smoking status, alcohol use status, serum 25-hydroxyvitamin D concentration, antidepressant use, and physical activity as measured by total vigorous and moderate metabolic equivalents. Subgroup analyses explored differences related to age. Results: QIDS-SR16 score was not a significant predictor of either lumbar spine or total hip T-score (β = -0.01, P = .61 and β = -0.02, P = .39) in the overall population (n = 2,285). There was a significant negative interaction term between age and QIDS-S16 group (β = -0.01, P = .01). In participants aged 60 years or older (n = 465), QIDS-S16 score was a significant predictor of BMD at the lumbar spine and total hip (β = -0.14, P = .003 and β = -0.12, P = .006, respectively). Conclusions: QIDS-S16 score did not significantly predict BMD in the overall DHS-2 sample. There was, however, a significant association observed in participants aged ≤ 60 years. Results suggest that diagnosis and treatment of depressive symptoms may be of clinical importance in older individuals, a subgroup at high risk for osteoporosis and fractures.
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U2 - 10.4088/JCP.16m11276
DO - 10.4088/JCP.16m11276
M3 - Article
C2 - 28837274
AN - SCOPUS:85049440067
SN - 0160-6689
VL - 79
SP - 22
EP - 27
JO - Journal of Clinical Psychiatry
JF - Journal of Clinical Psychiatry
IS - 3
ER -