Association between mood episode severity and c-reactive protein levels in bipolar disorder: an exploratory cross-sectional study
DOI:
https://doi.org/10.18203/2394-6040.ijcmph20263181Keywords:
Bipolar disorder, Inflammation, Mania, Depression, C-reactive proteinAbstract
Background: Bipolar disorder is a chronic, recurrent mood disorder associated with significant disability, functional impairment, and medical comorbidities. Increasing evidence suggests that immune-inflammatory mechanisms contribute to its pathophysiology. C-reactive protein (CRP), a widely used biomarker of systemic inflammation, has been reported to be elevated in bipolar disorder, particularly during manic episodes. However, data from the Indian population examining the association between CRP levels and severity of mood episodes using standardized rating scales remain limited. Therefore, this study was conducted to evaluate the association between severity of manic and depressive episodes and serum CRP levels in patients with bipolar disorder.
Methods: This hospital-based cross-sectional analytical study was conducted at a tertiary care center. Thirty patients diagnosed with bipolar disorder were assessed during either a manic episode (n=15) or a depressive episode (n=15). Severity was evaluated using the young mania rating scale (YMRS) and Hamilton depression rating scale (HAM-D). Serum CRP levels were measured and categorized as normal (≤5 mg/l) or elevated (>5 mg/l). Correlations were analysed using Pearson’s correlation coefficient.
Results: Fourteen participants (46.7%) had elevated CRP levels. Mean CRP levels were higher in manic episodes (17.82±16.38 mg/l) than depressive episodes (9.80±8.14 mg/l). A significant positive correlation was found between YMRS scores and CRP levels (r=0.5622, p=0.0292), whereas no significant correlation was observed between HAM-D scores and CRP levels (r=−0.1672, p=0.5515).
Conclusions: Severity of manic symptoms is positively associated with systemic inflammation, supporting inflammation as a state-dependent correlate of mania.
References
Merikangas KR, Jin R, He JP, Kessler RC, Lee S, Sampson NA, et al. Prevalence and correlates of bipolar spectrum disorder in the world mental health survey initiative. Arch Gen Psychiatr. 2011;68(3):241-51.
Ferrari AJ, Stockings E, Khoo JP, Erskine HE, Degenhardt L, Vos T, et al. The prevalence and burden of bipolar disorder: findings from the Global Burden of Disease Study 2013. Bipol Disord. 2016;18(5):440-50.
Gautham MS, Gururaj G, Varghese M, Benegal V, Rao GN, Kokane A, et al. The National Mental Health Survey of India (2016): prevalence, socio-demographic correlates and treatment gap of mental morbidity. Int J Soc Psychiatr. 2020;66(4):361-72.
Kapczinski F, Dal-Pizzol F, Teixeira AL, Magalhaes PVS, Kauer-Sant’Anna M, Klamt F, et al. Peripheral biomarkers and illness activity in bipolar disorder. J Psychiatr Res. 2011;45(2):156-61.
Dargél AA, Godin O, Kapczinski F, Kupfer DJ, Leboyer M. C-reactive protein alterations in bipolar disorder: a meta-analysis. J Clin Psychiatr. 2015;76(2):142-50.
Sundaresh A, Rajkumar RP, Krishnamoorthy R, Leboyer M, Negi VS, Tamouza R. C-reactive protein in bipolar disorder in an indian clinical setting. J Clin Diagn Res. 2018;12(9).
Wysokiński A, Margulska A, Strzelecki D, Kłoszewska I. Levels of c-reactive protein (CRP) in patients with schizophrenia, unipolar depression and bipolar disorder. Nord J Psychiatr. 2015;69(5):346-53.
Poletti S, Mazza MG, Benedetti F. Inflammatory mediators in major depression and bipolar disorder. Transl Psychiatr. 2024;14:247.