Lower pro- to anti-inflammatory ratios associated with reduced neurocognitive flexibility in symptomatic adolescents with bipolar disorder

Rahmani, Noreen; Hatch, Jessica; Dimick, Mikaela K.; Naiberg, Melanie R.; Fiksenbaum, Lisa; Andreazza, Ana Cristina; Bowie, Christopher R.; Dickstein, Daniel P.; Goldstein, Benjamin I.

doi:10.1016/j.jad.2021.05.062

Cited by 7 publications

(1 citation statement)

References 79 publications

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“…However, there is a gap in the knowledge regarding the association between CRP and brain structure in youth. This is important given that adolescence is a critical period of brain development ( Jalbrzikowski et al, 2019 ), and elevated inflammation may be particularly relevant in the early-stage BD ( Kauer-Sant’Anna et al, 2009 ; Rahmani et al, 2021 ; Wu et al, 2022 ).…”

Section: Introductionmentioning

confidence: 99%

Higher Levels of C-reactive Protein Are Associated With Higher Cortical Surface Area and Lower Cortical Thickness in Youth With Bipolar Disorder

Shao,

Zou,

Kennedy

et al. 2023

International Journal of Neuropsychopharmacology

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Background Inflammation is implicated in the neuropathology of bipolar disorder (BD). The association of C-reactive protein (CRP) with brain structure has been examined in relation to BD among adults but not youth. Methods Participants included 101 youth (BD, n=55; control group [CG], n=46; aged 13-20 years). Blood samples were assayed for levels of CRP. T1-weighted brain images were acquired to obtain cortical surface area (SA), volume, and thickness for three regions of interest (ROI; whole-brain cortical gray matter, prefrontal cortex (PFC), orbitofrontal cortex (OFC)) and for vertex-wise analyses. Analyses included CRP main-effects and interaction effects controlling for age, sex, and intracranial volume. Results In ROI analyses, higher CRP was associated with higher whole-brain SA (β=0.16; p=0.03), lower whole-brain (β=-0.31; p=0.03) and OFC cortical thickness (β=-0.29; p=0.04) within the BD group, and was associated with higher OFC SA (β=0.17; p=0.03) within CG. In vertex-wise analyses, higher CRP was associated with higher SA and lower cortical thickness in frontal and parietal regions within BD. A significant CRP-by-diagnosis interaction was found in frontal and temporal regions, whereby higher CRP was associated with lower neurostructural metrics in the BD group but higher neurostructural metrics in CG. Conclusions This study found that higher CRP among youth with BD is associated with higher SA but lower cortical thickness in ROI and vertex-wise analyses. The study identified two regions in which the association of CRP with brain structure differs between youth with BD vs. CG. Future longitudinal, repeated-measures studies incorporating additional inflammatory markers are warranted.

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