Dissecting the genetic association of C-reactive protein with PTSD, traumatic events, and social support.

Journal: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology

Volume: 46

Issue: 6

Year of Publication: 2021

Affiliated Institutions:  Department of Psychiatry, Yale School of Medicine and VA CT Healthcare Center, West Haven, CT, , USA. Department of Psychiatry, School of Medicine, University of California, San Diego, La Jolla, CA, USA. MRC Unit on Risk & Resilience in Mental Disorders, Department of Psychiatry and Neuroscience Institute, University of Cape Town, Cape Town, South Africa. Department of Psychology, University of California, Los Angeles, Los Angeles, CA, USA. Department of Psychiatry, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa. Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA. Department of Psychiatry, Universidade Federal de São Paulo (UNIFESP), São Paulo, SP, Brazil. Department of Psychiatry, Yale School of Medicine and VA CT Healthcare Center, West Haven, CT, , USA. renato.polimanti@yale.edu.

Abstract summary 

Inflammatory markers like C-reactive protein (CRP) have been associated with post-traumatic stress disorder (PTSD) and traumatic experiences, but the underlying mechanisms are unclear. We investigated the relationship among serum CRP, PTSD, and traits related to traumatic events and social support using genetic association data from the Psychiatric Genomics Consortium (23,185 PTSD cases and 151,309 controls), the UK Biobank (UKB; up to 117,900 individuals), and the CHARGE study (Cohorts for Heart and Aging Research in Genomic Epidemiology, 148,164 individual). Linkage disequilibrium score regression, polygenic risk scoring, and two-sample Mendelian randomization (MR) analyses were used to investigate genetic overlap and causal relationships. Genetic correlations of CRP were observed with PTSD (rg = 0.16, p = 0.026) and traits related to traumatic events, and the presence of social support (-0.28 < rg < 0.20; p < 0.008). We observed a bidirectional association between CRP and PTSD (CRP → PTSD: β = 0.065, p = 0.015; PTSD → CRP: β = 0.008, p = 0.009). CRP also showed a negative association with the "felt loved as a child" trait (UKB, β = -0.017, p = 0.008). Owing to the known association of socioeconomic status (SES) on PTSD, a multivariable MR was performed to investigate SES as potential mediator. We found that household income (univariate MR: β = -0.22, p = 1.57 × 10; multivariate MR: β = -0.17, p = 0.005) and deprivation index (univariate MR: β = 0.38, p = 1.63 × 10; multivariate MR: β = 0.27, p = 0.016) were driving the causal estimates of "felt loved as a child" and CRP on PTSD. The present findings highlight a bidirectional genetic association between PTSD and CRP, also suggesting a potential role of SES in the interplay between childhood support and inflammatory processes with respect to PTSD risk.

Authors & Co-authors:  Muniz Carvalho Carolina C Wendt Frank R FR Maihofer Adam X AX Stein Dan J DJ Stein Murray B MB Sumner Jennifer A JA Hemmings Sian M J SMJ Nievergelt Caroline M CM Koenen Karestan C KC Gelernter Joel J Belangero Sintia I SI Polimanti Renato R

Study Outcome 

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Statistics
Citations :  North CS, Suris AM, Smith RP, King RV. The evolution of PTSD criteria across editions of DSM. Ann Clin Psychiatry. 2016;28:197–208.
Authors :  12
Identifiers
Doi : 10.1038/s41386-020-0655-6
SSN : 1740-634X
Study Population
Male,Female
Mesh Terms
C-Reactive Protein
Other Terms
Study Design
Cross Sectional Study
Study Approach
Country of Study
Publication Country
England