Elevated C-reactive protein and late-onset bipolar disorder in 78 809 individuals from the general population

Br J Psychiatry. 2016 Feb;208(2):138-45. doi: 10.1192/bjp.bp.114.150870. Epub 2015 Aug 6.

Abstract

Background: No prospective studies have examined the role of C-reactive protein (CRP) in late-onset bipolar disorder.

Aims: We tested the hypothesis that elevated levels of CRP are associated cross-sectionally and prospectively with late-onset bipolar disorder, and that such an association possibly is causal.

Method: We performed cross-sectional and prospective analyses with a median follow-up time of 5.9 years (interquartile range: 4.4-7.6) in 78 809 individuals from the general population, and used genetic variants influencing CRP levels to perform a Mendelian randomisation study.

Results: Elevated levels of CRP were associated both cross-sectionally and prospectively with late-onset bipolar disorder. When CRP was on a continuous scale, a doubling in CRP yielded an observational odds ratio for late-onset bipolar disorder of 1.28 (1.08-1.52) with a corresponding causal odds ratio of 4.66 (0.89-24.3).

Conclusion: Elevated CRP is associated with increased risk of late-onset bipolar disorder in the general population which was supported by the genetic analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Bipolar Disorder / blood*
  • Bipolar Disorder / genetics
  • C-Reactive Protein / analysis*
  • C-Reactive Protein / genetics*
  • Cross-Sectional Studies
  • Female
  • Humans
  • Late Onset Disorders / blood*
  • Late Onset Disorders / genetics
  • Logistic Models
  • Male
  • Mendelian Randomization Analysis
  • Middle Aged
  • Odds Ratio
  • Polymorphism, Single Nucleotide
  • Prospective Studies
  • Risk Factors

Substances

  • C-Reactive Protein