Adverse Childhood Experiences and Risk for First-Episode Major Depression During the Menopause Transition

作者：Epperson C Neill^*; Sammel Mary D; Bale Tracy L; Kim Deborah R; Conlin Sarah; Scalice Stephanie; Freeman Katharine; Freeman Ellen W

来源：Journal of Clinical Psychiatry, 2017, 78(3): E298-+.

DOI：10.4088/JCP.16m10662

Objective: Stress exposures may have a differential impact on risk and resilience for depression depending on their timing across development. We sought to determine whether adverse childhood experiences (ACEs) and their onset with respect to puberty contribute to the increased risk observed in firstepisode major depressive disorder (MDD) during the menopause transition.
Methods: Participants were from the Penn Ovarian Aging Study cohort, which is composed of women from Philadelphia County, Pennsylvania, who underwent behavioral, cognitive, and endocrine evaluations approximately yearly from 1996 to 2012 and completed the Adverse Childhood Experiences Questionnaire at study end point (n = 243). ACEs that first occurred 2 or more years before menarche were considered prepubertal. Incident menopause MDD was defined as first observed onset of the disorder in the perimenopause to postmenopause transition using the Structured Clinical Interview for DSM-III-R and the Primary Care Evaluation of Mental Disorders.
Results: Incident menopause MDD occurred in 48% of the 100 women who reported lifetime MDD. Women reporting >= 2 total ACEs were at significantly greater risk for lifetime MDD (adjusted odds ratio [aOR] = 2.05, P =.034) and incident menopause MDD (aOR = 2.58, P =.03) compared to those reporting 0 ACEs; women with >= 2 postpubertal ACEs were 2.3 times more likely to experience incidence menopause MDD (P =.024) after controlling for race, smoking, body mass index, and employment. Experiencing only 1 ACE in the prepubertal window, regardless of additional ACEs in postpuberty, was associated with reduced risk for lifetime and incident menopause MDD.
Conclusions: Timing and number of adverse experiences with respect to puberty differentially impacted risk and resilience for MDD across the female life span and during the menopause transition in this community cohort.

• 出版日期2017-3