PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 11, 20250 citationsOpen Access

Neural correlates of adverse childhood experiences, depression and chronic pain in the reward system

GAGeorgia AntoniouBSBlair H. SmithLRLiana Romaniuk

Key Result

Individuals reporting both adverse childhood experiences and chronic pain exhibited significantly reduced volume in the nucleus accumbens compared to those with neither condition (Cohen's d = 0.39).

Study Design

Type

Cohort (n=847)

Multicenter

Yes

Structured PICO

P
Population
847 community-based adults (mean age 59.03, 62% female) from the Generation Scotland cohort with structural MRI data, including subsets with fMRI data (n=604) and both (n=552).
O
Outcome
Structural (grey matter volume) and functional (reward-related activation) changes in the brain's reward system (basal ganglia/nucleus accumbens)surrogate

Adverse childhood experiences, chronic pain, and depression are associated with distinct but converging structural and functional alterations in the brain's reward system.

Main Result

Effect estimate: Cohen's d 0.39

p-value: p=0.006

Limitations

  • Retrospective assessment of ACEs introduces potential recall bias
  • Chronic pain and depression may impact the retrospective recall of ACEs
  • Chronic pain was measured before imaging and mood assessments
  • The reward task was brief
  • The sample was non-clinical and community-based, which may underestimate effects present in clinical populations
  • Retrospective assessment of ACEs introduces recall bias
  • Chronic pain measured 3-11 years before imaging and mood assessments
  • Brief reward task
  • Non-clinical community-based sample may underestimate effects

Abstract

Abstract Adverse childhood experiences (ACEs) are common, altering behaviour and stress reactivity, with persistent structural and functional brain changes. ACEs are associated with a greater risk of physical and mental health morbidities, including depression and chronic pain (CP), which often co-exist. While changes in the reward system have been implicated in each condition, it remains unclear whether there are common neural mechanisms. Using brain scans from a large community sample, we examined how ACEs, depression, and CP affected the reward system. Individuals reporting both ACEs and CP exhibited reduced volume in the nucleus accumbens, a brain region associated with motivation and pleasure, particularly among women. Blunted reward-related activity in the basal ganglia was linked to higher depression scores, CP severity, and experiences of childhood sexual abuse. Importantly, these functional changes remained significant even after accounting for structural brain differences. Interestingly, brain structural-functional associations were weak, suggesting distinct underlying mechanisms. Structural brain alterations likely represent cumulative, enduring consequences of ACEs and CP, whereas altered reward activity appears more closely tied to current symptom severity. These findings reveal separable but converging neurobiological signatures of early adversity, pain, and depression within the brain’s reward system.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Antoniou et al. (2025) conducted a cohort in Adverse childhood experiences, depression, and chronic pain (n=847). Adverse childhood experiences and chronic pain vs. No adverse childhood experiences and no chronic pain was evaluated on Nucleus accumbens (NAcc) volume (Cohen's d 0.39, p=0.006). Individuals reporting both adverse childhood experiences and chronic pain exhibited significantly reduced volume in the nucleus accumbens compared to those with neither condition (Cohen's d = 0.39).

synapsesocial.com/papers/6a1ac049837f1a2c63b9058chttps://doi.org/10.1101/2025.07.10.25331260
Ask AI
Helpful
Bookmark
Share
View Full Paper