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PreprintCC BY 4.0PsyArXiv

The Role of Menstrual Cycle Phase in PTSD: A Scoping Review of Symptom Expression, Neuropsychology and Psychotherapy Response in Women

Abstract

Women are diagnosed with post-traumatic stress disorder (PTSD) at twice the rate of men, a disparity only partly explained by trauma exposure differences. Sex-specific biological factors, particularly cyclic fluctuations in estradiol and progesterone, have been associated with PTSD symptoms/related neuropsychological processes in healthy/trauma exposed women; however, the extent and clinical translation of this literature (if any) remain unclear in PTSD populations. This review aimed to map evidence examining associations between ovarian hormones/menstrual cycle phase and PTSD symptoms and/or related neuropsychological processes (e.g., extinction learning) in women with PTSD (Aim1), and/or associations with psychotherapy outcomes in PTSD/related anxiety disorders (Aim2). A systematic search for peer-reviewed, empirical studies involving adult females was conducted across 6 databases, in accordance with PRISMA-ScR and JBI guidelines. From 2,464 results, 12 studies were included. Five studies addressed Aim 1 and seven addressed Aim 2. Hormonal operationalization was inconsistent, including continuous assays (n=5), menstrual cycle phase comparisons (n=3), and/or median split/other groupings (n=6), with estradiol most frequently measured. For Aim 1, PTSD symptom findings were inconsistent and inconclusive (n=3), whereas lower estradiol was more consistently associated with impaired fear extinction and habituation (n=2). For Aim 2, findings in anxiety-related disorders were mixed, with no study examining ovarian hormone status in psychotherapy outcomes for women with PTSD. Overall, evidence remains sparse, heterogeneous and largely cross-sectional. Findings do not yet support firm conclusions regarding ovarian hormone–PTSD symptom/neuropsychological interactions but highlight key research gaps and future directions to better understand these relationships and inform personalized PTSD treatments for women.

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BibTeX
@misc{treacy2026role,
  title = {{The Role of Menstrual Cycle Phase in PTSD: A Scoping Review of Symptom Expression, Neuropsychology and Psychotherapy Response in Women}},
  author = {Ciara Treacy and Mia Schaumberg and Katherine Moore and Ella Liow and Sophie Andrews and Bronwyn Graham and Alain Brunet},
  howpublished = {PsyArXiv},
  year = {2026},
  month = oct,
  doi = {10.31234/osf.io/a6cy2_v1},
  url = {https://osf.io/preprints/psyarxiv/a6cy2_v1/},
  note = {CC BY 4.0},
}
RIS
TY  - UNPB
TI  - The Role of Menstrual Cycle Phase in PTSD: A Scoping Review of Symptom Expression, Neuropsychology and Psychotherapy Response in Women
AU  - Ciara Treacy
AU  - Mia Schaumberg
AU  - Katherine Moore
AU  - Ella Liow
AU  - Sophie Andrews
AU  - Bronwyn Graham
AU  - Alain Brunet
PY  - 2026
DA  - 2026/10/30
PB  - PsyArXiv
DO  - 10.31234/osf.io/a6cy2_v1
UR  - https://osf.io/preprints/psyarxiv/a6cy2_v1/
AB  - Women are diagnosed with post-traumatic stress disorder (PTSD) at twice the rate of men, a disparity only partly explained by trauma exposure differences. Sex-specific biological factors, particularly cyclic fluctuations in estradiol and progesterone, have been associated with PTSD symptoms/related neuropsychological processes in healthy/trauma exposed women; however, the extent and clinical translation of this literature (if any) remain unclear in PTSD populations. This review aimed to map evidence examining associations between ovarian hormones/menstrual cycle phase and PTSD symptoms and/or related neuropsychological processes (e.g., extinction learning) in women with PTSD (Aim1), and/or associations with psychotherapy outcomes in PTSD/related anxiety disorders (Aim2). A systematic search for peer-reviewed, empirical studies involving adult females was conducted across 6 databases, in accordance with PRISMA-ScR and JBI guidelines. From 2,464 results, 12 studies were included. Five studies addressed Aim 1 and seven addressed Aim 2. Hormonal operationalization was inconsistent, including continuous assays (n=5), menstrual cycle phase comparisons (n=3), and/or median split/other groupings (n=6), with estradiol most frequently measured. For Aim 1, PTSD symptom findings were inconsistent and inconclusive (n=3), whereas lower estradiol was more consistently associated with impaired fear extinction and habituation (n=2). For Aim 2, findings in anxiety-related disorders were mixed, with no study examining ovarian hormone status in psychotherapy outcomes for women with PTSD. Overall, evidence remains sparse, heterogeneous and largely cross-sectional. Findings do not yet support firm conclusions regarding ovarian hormone–PTSD symptom/neuropsychological interactions but highlight key research gaps and future directions to better understand these relationships and inform personalized PTSD treatments for women.
ER  -