C-reactive protein concentration in bipolar disorder: association with genetic variants

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Several recent studies have investigated the role of C-reactive protein (CRP) in bipolar disorder (BD), but few studies have directly investigated the interaction between CRP genetic variants and peripheral CRP concentration across different phases of BD. In this study, we aimed to replicate previous findings that demonstrated altered CRP levels in BD, and to investigate whether there is an association of peripheral protein expression with genetic variants in the CRP gene. Methods: 221 patients were included in the study, of which 183 (all episodes, 46 not medicated, 174 medicated) were genotyped for CRP single-nucleotide polymorphisms (SNPs) shown to influence peripheral CRP protein expression (rs1800947, rs2808630, rs1417938, rs1205). Results: There were no differences in CRP levels associated with the genotypes, only regarding the rs1205 SNP there were significantly different CRP protein expression between the genotypes when taking body mass index, age, BD polarity, subtype and leukocyte number into account. However, we could show significantly elevated CRP protein expression in manic patients compared to euthymic and depressed patients, independent from genotype. Medication was found to have no effect on CRP protein expression. Conclusions: These results indicate that low grade inflammation might play a role in mania and might be rather a state than a trait marker of bipolar disorder.

Original languageEnglish
Article number26
JournalInternational Journal of Bipolar Disorders
Volume7
Issue number1
DOIs
Publication statusPublished - 1 Dec 2019
Externally publishedYes

Keywords

  • Biomarker
  • Bipolar disorder
  • C-reactive protein
  • Genotype
  • Inflammation

Fingerprint

Dive into the research topics of 'C-reactive protein concentration in bipolar disorder: association with genetic variants'. Together they form a unique fingerprint.

Cite this