Inflammatory cytokines and cognitive functioning in early-stage bipolar I disorder

• Published in: Journal of affective disorders Vol. 245; pp. 679 - 685
• Main Authors: Chakrabarty, Trisha, Torres, Ivan J., Bond, David J., Yatham, Lakshmi N.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 15.02.2019
• Subjects: Bipolar disorder; Cognition; Cytokines; Inflammation; Bipolar disorder; Inflammation; Cognition; Cytokines
• ISSN: 0165-0327; 1573-2517
• DOI: 10.1016/j.jad.2018.11.018

•Inflammatory cytokines have been associated with cognitive dysfunction in BDI.•Yet, the relationship between cytokines and cognition in early stage BDI is unclear.•In this sample of early stage patients, TNFα was associated with poorer cognition.•IL-6, IL-1α, IL-4 and IL-10 levels were not significantly associated with cognition.•Thus, TNFα may be a unique mediator of cognitive dysfunction in early BDI. Increased circulating inflammatory cytokines is a replicated finding in bipolar I disorder (BDI). Pro-inflammatory cytokines such as TNFα, IL-6 and IL-1 have also been associated with poorer cognitive functioning in patients with longer illness duration. However, the effect of inflammatory cytokines on cognition in early stage patients is not yet known. Here, we investigate the relationship between cytokines and cognition in BDI patients within three years of diagnosis. Serum pro-inflammatory (TNFα, IL-6 and IL-1α) and anti-inflammatory (IL-4 and IL-10) cytokine levels were compared between 51 early stage BDI patients and 20 healthy controls. 46 patients completed neuropsychological testing, and multiple regression analysis was used to assess the association between cytokine levels and cognition after accounting for relevant clinical and demographic variables. TNFα was elevated at trend level significance in BDI patients compared to healthy controls, and was negatively associated with global cognition, processing speed, and working memory in patients. IL-6, IL-1α, IL-4 and IL-10 levels were comparable between groups and were not significantly associated with cognition. Direct causation cannot be established in this cross-sectional study; in addition, cytokine levels were not taken on the same day as neuropsychological testing for all patients. TNFα may negatively impact cognition in early BDI. While replication is required in larger samples, these results suggest that inhibition of TNFα activity might be a strategy to preserve cognition in newly diagnosed BDI patients.