Structural brain changes with lifetime trauma and re-experiencing symptoms is 5-HTTLPR genotype-dependent
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Date
Authors
Ancelin, Marie-Laure
Carriere, Isabelle
Artero, Sylvaine
Maller, Jerome
Meslin, Chantal
Dupuy, Marie
Ritchie, K
Ryan, Joanne
Chaudieu, Isabelle
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Taylor & Francis
Abstract
Background: Findings on structural brain alterations following trauma are inconsistent due
probably to heterogeneity in imaging studies and population, clinical presentations, genetic
vulnerability, and selection of controls. This study examines whether trauma and reexperiencing symptoms are associated with specific alterations in grey matter volumes
and if this varies according to 5-HTTLPR genotype.
Methods: Structural MRI was used to acquire anatomical scans from 377 communitydwelling older adults. Quantitative regional estimates of 22 subregional volumes were
derived using FreeSurfer software. Lifetime trauma was assessed using the validated
Watson's PTSD inventory, which evaluates the most severe trauma experienced according
to DSM criteria. Analyses adjusted for age, sex, total brain volume, head injury, and
comorbidities.
Results: Of the 212 participants reporting lifetime trauma, 35.4% reported re-experiencing
symptoms and for 1.9%, this was severe enough to meet criteria for full threshold PTSD. In
participants with the SS 5-HTTLPR genotype only, re-experiencing symptoms were associated with smaller volumes in middle and superior temporal, frontal (lateral orbital, rostral
and caudal middle) and parietal (precuneus, inferior and superior) regions. The traumaexposed participants without re-experiencing symptoms were not significantly different
from the non-trauma-exposed participants except for smaller precuneus and superior
parietal region in traumatized participants and a larger amygdala in traumatized women
specifically.
Conclusions: In the non-clinical sample, lifetime trauma and re-experiencing symptoms
were associated with smaller volume in prefrontal, temporal and parietal cortex subregions,
and this varied according to serotonergic genetic vulnerability, 5-HTTLPR SS individuals
being most susceptible.
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European Journal of Psychotraumatology
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