Childhood maltreatment severity is associated with elevated C-reactive protein and body mass index in adults with schizophrenia and bipolar diagnoses

- Combined effects of childhood abuse experiences and clinical diagnosis on elevated hs-CRP.
- Childhood abuse experiences are linked to obesity.
- Dose-dependent effects of childhood maltreatment on higher BMI and hs-CRP.

BackgroundSeveral studies have described an association between childhood maltreatment and inflammatory markers in the psychotic disorders (schizophrenia [SZ] and bipolar disorder [BD]). Previous studies have been relatively small (<50 participants), and the severity of abuse and the putative influence of body mass index (BMI) have not been properly investigated.MethodsThe combined effects of childhood abuse severity and clinical diagnosis on inflammatory markers were investigated in a large sample (n = 483) of patients with a disorder on the psychosis spectrum and in healthy controls (HCs). Plasma levels of inflammatory markers (high-sensitivity C-reactive protein [hs-CRP], soluble tumor necrosis factor receptor type 1 [TNFR-R1], glycoprotein 130 [gp130]) were analyzed, and BMI and data on childhood trauma events, on the basis of the Childhood Trauma Questionnaire (CTQ), were obtained from all participants.ResultsPatients had increased levels of hs-CRP (P < 0.001, Cohens d = 0.4), lower levels of gp130 (P < 0.001, Cohens d = 0.5), higher BMI (P < 0.001, Cohens d = 0.5) and reported more childhood maltreatment experiences (P < 0.001, Cohens d = 1.2) than the HC group. The severity of childhood abuse (up to three types of abuse: sexual abuse, physical abuse, and emotional abuse) was associated with elevated BMI (f = 8.46, P < 0.001, Cohen's d = 0.5) and hs-CRP (f = 5.47, P = 0.001, Cohen's d = 0.3). Combined effects of patient status and severity of childhood abuse were found for elevated hs-CRP (f = 4.76, P < 0.001, Cohen's d = 0.4). Differences among the groups disappeared when BMI was added to the model.DiscussionTrauma-altered immune activation via elevated hs-CRP in patients with SZ and BD may be mediated by higher BMI; however, the direction of this association needs further clarification.