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A Systematic Review on the Bidirectional Relationship Between Trauma-related Psychopathology and Reproductive Aging

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Date 2025 Jan 13
PMID 39803367
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Abstract

Objective: Natural variation in ovarian steroid hormones across the female lifespan contributes to an increased risk for depressive and posttraumatic stress disorder (PTSD) symptoms in women. However, minimal work has focused on understanding the impacts of reproductive aging on the brain and behavioral health of trauma-exposed women. This systematic review examines the bidirectional relationship between trauma-related psychopathology and reproductive aging.

Method: Following PRISMA guidelines, a systematic review of PubMed, PsychInfo, and Medline databases was undertaken to identify controlled studies on how trauma history impacts psychopathology and menopause symptoms during reproductive aging.

Results: Twenty-one studies met the eligibility criteria, with only four utilizing the gold standard STRAW+ 10 criteria for defining reproductive aging stages. The peri and postmenopausal periods appear to be particularly vulnerable phases for individuals with trauma exposure. Menopause symptoms and trauma-related psychopathology symptom severity increase during reproductive aging with increases in the degree of trauma exposure. However, mechanistic insights that may explain this interaction are currently neglected in this area of research.

Conclusion: There is a significant lack of understanding regarding how reproductive aging and its related neuroendocrine changes impact the brain to influence PTSD and depression symptoms related to trauma exposure. This lack of basic understanding impedes the ability to identify, assess, and treat PTSD and depressive symptoms in trauma-exposed women most effectively, and mitigate the long-term consequences of these behavioral health symptoms on morbidity and mortality in aging women.

Citing Articles

Sex Differences in Endocannabinoid and Inflammatory Markers Associated with Posttraumatic Stress Disorder.

Rajasekera T, Joseph A, Pan H, Dreyfuss J, Fida D, Wilson J medRxiv. 2025; .

PMID: 39974010 PMC: 11838936. DOI: 10.1101/2025.01.13.25320467.

References
1.
Cohen L, Soares C, Vitonis A, Otto M, Harlow B . Risk for new onset of depression during the menopausal transition: the Harvard study of moods and cycles. Arch Gen Psychiatry. 2006; 63(4):385-90. DOI: 10.1001/archpsyc.63.4.385. View

2.
Wassertheil-Smoller S, Shumaker S, Ockene J, Talavera G, Greenland P, Cochrane B . Depression and cardiovascular sequelae in postmenopausal women. The Women's Health Initiative (WHI). Arch Intern Med. 2004; 164(3):289-98. DOI: 10.1001/archinte.164.3.289. View

3.
Kredlow M, Fenster R, Laurent E, Ressler K, Phelps E . Prefrontal cortex, amygdala, and threat processing: implications for PTSD. Neuropsychopharmacology. 2021; 47(1):247-259. PMC: 8617299. DOI: 10.1038/s41386-021-01155-7. View

4.
Shanmugan S, Satterthwaite T, Sammel M, Cao W, Ruparel K, Gur R . Impact of early life adversity and tryptophan depletion on functional connectivity in menopausal women: A double-blind, placebo-controlled crossover study. Psychoneuroendocrinology. 2017; 84:197-205. PMC: 5609529. DOI: 10.1016/j.psyneuen.2017.07.239. View

5.
Rasmusson A, Pinna G, Paliwal P, Weisman D, Gottschalk C, Charney D . Decreased cerebrospinal fluid allopregnanolone levels in women with posttraumatic stress disorder. Biol Psychiatry. 2006; 60(7):704-13. DOI: 10.1016/j.biopsych.2006.03.026. View