4.3 Article

Early Life Trauma and Social Processing in HIV: The Role of Neuroendocrine Factors and Inflammation

Journal

PSYCHOSOMATIC MEDICINE
Volume 84, Issue 8, Pages 874-884

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/PSY.0000000000001124

Keywords

early life trauma; HIV; inflammation; oxytocin; vasopressin; cortisol; social processing

Funding

  1. National Institute of Mental Health of the National Institutes of Health [K01MH098798, R21MH099978, R01MH113512]
  2. National Center for Advancing Translational Sciences, National Institutes of Health [UL1TR000050]
  3. University of Illinois at Chicago Campus Review Board Grant
  4. Chicago Developmental Center for AIDS Research pilot grant
  5. National Institute of Mental Health

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The study found that early life trauma may affect social processing in people with HIV, and oxytocin and C-reactive protein may be targets for improving social processing in individuals exposed to early life trauma.
Objective: Early life trauma (ELT) and HIV are associated with social processing deficits. In people with HIV (PWH), we examined whether facial emotion identification accuracy differs by ELT and whether neuroendocrine factors including cortisol, oxytocin (OT), and arginine vasopressin, and/or immune system measures play a role in the ELT-performance association. Methods: We used secondary data from the placebo condition of a pharmacologic challenge study in PWH. Presence of ELT was measured with the Childhood Trauma Questionnaire (at least moderate experiences of sexual, physical, and/or emotional abuse). Social processing was measured with the Facial Emotion Perception Test (FEPT). Salivary immune system measures and cortisol were sampled across a 5-hour study session. Blood was collected at study session start (12 PM) to measure OT and arginine vasopressin. We examined the association of ELT with FEPT and five biological moderators (from principal components analysis of 12 biomarkers) of ELT-FEPT associations. Results: Of 58 PWH (42 men; mean [standard deviation] age = 33.7 [8.9] years), 50% endorsed ELT. ELT-exposed PWH demonstrated lower identification accuracy across all emotional expressions (unstandardized beta[B] = 0.13; standard error [SE] = 0.05; p = .021, d = 0.63) and had higher OT levels compared with ELT-unexposed PWH (t((1,56)) = 2.12, p = .039; d = 0.57). For total accuracy, an OT/C-reactive protein factor moderated the ELT-FEPT association (B = 0.14; SE = 0.05; p = .014); accuracy was lower in ELT-exposed PWH versus ELT-unexposed PWH when the factor was low but not when high Similar results were obtained for fearful, neutral, and happy faces (p values < .05). Regardless of ELT, a myeloid migration (MCP-1/MMP-9) factor was associated with reduced accuracy (p values < .05). Conclusions: Our pilot findings suggest that ELT may alter social processing in PWH, and OT and C-reactive protein may be a target for improving social processing in ELT-exposed PWH, and myeloid migration markers may be a target in PWH more generally.

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