AI Insight
This large-scale neuroimaging study using UK Biobank data (N = 21,995) found that chronic pain and trauma exposure are each independently associated with alterations in white matter microstructure, measurable via fractional anisotropy and mean diffusivity. When analyzed together, chronic pain was linked to changes concentrated in brainstem tracts and the cingulum, while cumulative trauma severity showed broader alterations including frontal and parietal tracts, and childhood maltreatment specifically affected brainstem tracts, the sagittal stratum, and the superior longitudinal fasciculus. These effects were more pronounced in females, and an interactive effect between chronic pain and childhood maltreatment severity was identified in the superior cerebellar peduncle in females.
Why it matters
The findings suggest that clinical approaches to chronic pain should account for patients' trauma history, the developmental timing of that trauma, and the patient's sex, as these factors appear to shape distinct neurological profiles. This supports the integration of trauma-informed, sex-sensitive care frameworks into pain management practices.
⚠️ Preprint – Noch nicht peer-reviewed
Dieser Artikel wurde noch nicht von unabhängigen Experten begutachtet. Die Ergebnisse sind vorläufig und sollten mit Vorsicht interpretiert werden.
Background. Lifetime exposure to trauma is associated with chronic pain. Separate studies of chronic pain and trauma report overlapping alterations in white matter microstructure, yet their distinct and cumulative effects remain unclear. Methods. White matter microstructure (fractional anisotropy [FA] and mean diffusivity [MD]) from the UK Biobank (N = 21,995) were analysed using linear mixed-effects models. First, group effects (chronic pain versus control) on white matter integrity within this cohort were established. To investigate distinct and cumulative impacts of trauma exposure at different developmental stages, main and interactive effects of group and trauma severity on FA and MD were examined in separate groups exposed to childhood maltreatment only, adulthood trauma only, and both. Sex-stratified analyses were conducted. Results. Chronic pain was associated with widespread alterations and was spatially refined to brainstem tracts and cingulum when accounting for maltreatment/trauma severity. Accounting for chronic pain, cumulative trauma severity was associated with alterations in brainstem, frontal and parietal tracts, whereas adulthood trauma showed comparable but attenuated patterns. Childhood maltreatment severity was associated with localised FA and MD reductions in brainstem tracts, sagittal stratum and superior longitudinal fasciculus. These effects were more pronounced in females than males. A chronic pain-by-maltreatment/trauma severity interaction was observed for FA in the superior cerebellar peduncle in females exposed to childhood maltreatment only. Conclusions. Distinct and interactive effects of chronic pain and maltreatment/trauma severity on white matter microstructure were evident. The findings suggest that trauma-informed care should be tailored by timing of exposure and sex in this population.
Source: White matter markers of chronic pain and trauma in UK Biobank