Bone mineral density and bone metabolism in patients with major depressive disorder without somatic comorbidities

Prog Neuropsychopharmacol Biol Psychiatry. 2013 Jul 1:44:58-63. doi: 10.1016/j.pnpbp.2013.01.019. Epub 2013 Feb 1.

Abstract

Background: Major depressive disorder (MDD) has been linked with accelerated bone loss leading to the development of low bone mineral density (BMD). Several mechanisms have been discussed as causative factors, e.g. lifestyle, selective serotonin reuptake inhibitor (SSRI) intake, or the influence of proinflammatory cytokines.

Methods: In a cross-sectional study of in-patients with a current episode of MDD, without somatic comorbidities, we determined various parameters of bone metabolism, inflammatory parameters and parameters of depression. BMD was measured by dual x-ray absorptiometry.

Results: Of 50 patients, only one had low BMD in any of the measure sites. Body mass index (BMI) correlated positively with Z-scores. 83.3% of the examined patients had elevated osteoprotegerin (OPG) levels. SSRI intake did not have an effect on BMD. BMD in the femoral neck was significantly lower in smokers. We also found a positive correlation between the level of physical activity and osteocalcin levels.

Conclusions: In our sample, young to middle-aged, somatically healthy, and acutely depressed patients with a history of MDD showed no reduction of BMD. This could be due to compensatory mechanisms, as suggested by elevated OPG levels. Physical activity and high BMI could also have served as protective factors. Still, as patients with MDD often suffer from comorbidities or take medication with a negative effect on bone, this population should be appreciated as a high-risk group for the development of osteopenia and osteoporosis.

MeSH terms

  • Absorptiometry, Photon
  • Adult
  • Body Mass Index
  • Bone Density / physiology*
  • Bone and Bones / metabolism*
  • Cytokines / metabolism
  • Depressive Disorder, Major / complications*
  • Female
  • Humans
  • Male
  • Metabolic Diseases / pathology*
  • Middle Aged
  • Osteoprotegerin / metabolism
  • Young Adult

Substances

  • Cytokines
  • Osteoprotegerin