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Major Depressive Disorder and Bone Mass in Adolescents and Young Adults
Journal article   Open access   Peer reviewed

Major Depressive Disorder and Bone Mass in Adolescents and Young Adults

Chadi A Calarge, Brandon D Butcher, Trudy L Burns, William H Coryell, Janet A Schlechte and Babette S Zemel
Journal of bone and mineral research, Vol.29(10), pp.2230-2237
10/2014
DOI: 10.1002/jbmr.2249
PMCID: PMC5520808
PMID: 24723424
url
https://doi.org/10.1002/jbmr.2249View
Published (Version of record) Open Access

Abstract

Depression has been associated with reduced bone mass in adults, but the mechanisms remain unclear. In addition, little is known about the association between depression and bone health during growth and development. To address this knowledge gap, we examined bone density and structure in 222 adolescents and young adults (69% females, mean ± SD age: 19.0 ± 1.5 years), enrolled within 1 month of starting a selective serotonin reuptake inhibitor (SSRI) or unmedicated. Psychiatric functioning was assessed with self‐report and researcher‐administered instruments, including the Longitudinal Interval Follow‐up Evaluation for Adolescents (A‐LIFE). Anthropometric and laboratory measures included dual‐energy x‐ray absorptiometry and peripheral quantitative computed tomography scans. Linear multivariable regression analysis tested the association between depression and bone mass, after accounting for relevant confounders. The presence of current depression was associated with a significant reduction in age‐sex‐height‐race‐specific bone mineral density (BMD) and content (BMC) of total body less head and lumbar spine. The findings varied by assessment method with self‐report scales, capturing symptom severity over the prior week or two, yielding the weakest associations. Depression was also associated with reduced cortical thickness and a trend for increased endosteal circumference. In contrast, generalized anxiety disorder was not associated with bone deficits. In sum, depressive illness is associated with significantly lower bone mass in youths. Future investigations must examine whether bone recovery is possible following depression remission or whether remedial interventions are warranted to optimize bone mass in order to minimize the long‐term risk of osteoporosis. © 2014 American Society for Bone and Mineral Research.
BONE‐BRAIN‐NERVOUS SYSTEM INTERACTIONS DXA BONE QCT/microCT

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