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Updated: Feb 24, 2026

Scanning Skeletal Remains for Bone Mineral Density in Forensic Contexts
Published on: January 29, 2018
Association Between Bone Mineral Density and Depressive Symptoms in a Population-Based Sample
Rocco D Hlis1, Roger S McIntyre2, Naim M Maalouf3
1Department of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
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-SR₁₆), 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-SR₁₆ 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-SR₁₆ group (β = -0.01, P = .01). In participants aged 60 years or older (n = 465), QIDS-SR₁₆ 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-SR₁₆ 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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