Frontiers in Psychiatry (Jun 2020)

Association Between Bipolar Disorder and Low Bone Mass: A Cross-Sectional Study With Newly Diagnosed, Drug-Naïve Patients

  • Sujuan Li,
  • Sujuan Li,
  • Yan Qui,
  • Yan Qui,
  • Ziwei Teng,
  • Ziwei Teng,
  • Jindong Chen,
  • Jindong Chen,
  • Dongyu Kang,
  • Dongyu Kang,
  • Hui Tang,
  • Hui Tang,
  • Hui Xiang,
  • Hui Xiang,
  • Chujun Wu,
  • Chujun Wu,
  • Yuxi Tan,
  • Yuxi Tan,
  • Lu Wang,
  • Lu Wang,
  • Yanyi Yang,
  • Bolun Wang,
  • Haishan Wu,
  • Haishan Wu

DOI
https://doi.org/10.3389/fpsyt.2020.00530
Journal volume & issue
Vol. 11

Abstract

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BackgroundMedical comorbidities in people with mental disorders have recently gained more attention. People with bipolar disorder (BD) often have comorbid low bone mass, which is associated with increased fracture risk and related severe outcomes. However, few clinical studies on bone metabolism in BD patients are available. This study was designed to assess bone mineral density (BMD) and related influencing factors in a sample of newly diagnosed, drug-naïve individuals with BD and age- and sex-matched healthy controls.MethodsSixty-one drug-naïve individuals with BD (DSM-V) and 95 healthy volunteers had their lumbar spine (L1–L4) and left hip (Neck/Troch/Ward's) BMD determined by dual-energy X-ray absorptiometry. Besides, sociodemographic and clinical assessment were collected. Between-group comparisons and within subgroup analysis were performed.ResultsDrug-naïve patients with BD had significantly lower BMD in comparison to healthy controls in multiple sites (L1, L3, Neck, Troch, Ward's, and total hip). On subgroup analysis, overweight individuals with BD had higher bone mass, while females presented reduced BMD. Binary logistic regression showed that low BMD in multiple regions was associated with BD diagnosis, body mass index (BMI), gender, and age.ConclusionDrug-naïve individuals with BD have lower BMD when compared to an age- and gender-matched healthy control sample. Low BMI and female gender are factors associated with this outcome. The underlying pathological mechanisms of BD comorbid with osteoporosis should be further explored.Clinical Trial Registrationwww.chictr.org.cn, identifier ChiCTR190002137.

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