Abstract
Fluctuations in progesterone (P4) and estradiol (E2) across the menstrual cycle can exert direct effects on biological systems implicated in neuropsychiatric disorders and represent a key biological source of variability in affective, cognitive, and behavioral disorders. Although these cyclical symptoms may be most readily identified when they occur exclusively in relation to the menstrual cycle, as in DSM-5 premenstrual dysphoric disorder, symptom changes of similar magnitude occur in a larger proportion of people with ongoing psychiatric disorders. Studies investigating cyclical regulation of brain and behavior often produce inconsistent results, which may be attributed to a lack of focus on specific hormonal events and individual differences in related sensitivities. We propose a transdiagnostic Dimensional Affective Sensitivity to Hormones across the Menstrual Cycle (DASH-MC) framework, postulating that atypical neural responses to several key hormonal events provoke specific temporal patterns of affective and behavioral change across the menstrual cycle. We review prospective and experimental evidence providing initial support for these dimensions, which include (1) luteal-onset negative affect caused by a sensitivity to E2 or P4 surges (mediated by neuroactive metabolites such as allopregnanolone), typified by irritability and hyperarousal; (2) perimenstrual-onset negative affect caused by a sensitivity to low or falling E2, typified by low mood and cognitive dysfunction; and (3) preovulatory-onset positive affect dysregulation caused by a sensitivity to E2 surges, typified by harmful substance use and other risky reward-seeking. This multidimensional, transdiagnostic framework for hormone sensitivity can inform more precise research on ovarian steroid regulation of psychopathology, including further mechanistic research, diagnostic refinement, and precision psychiatry treatment development. Additionally, given the high rates of hormone sensitivity across affective disorders, the DASH-MC may guide broader insights into the complex neurobiological vulnerabilities driving female-biased affective risk, as well as potential triggers and mechanisms of affective state change in psychiatric disorders.
| Original language | English |
|---|---|
| Article number | 100194 |
| Pages (from-to) | 251-262 |
| Number of pages | 12 |
| Journal | Molecular Psychiatry |
| Volume | 30 |
| Issue number | 1 |
| DOIs | |
| State | Published - Jan 2025 |
Bibliographical note
Publisher Copyright:© The Author(s), under exclusive licence to Springer Nature Limited 2024.
Funding
The authors thank the many patients, study participants, and advocates (especially the International Association for Premenstrual Disorders) whose invaluable contributions have allowed us to develop this framework. The authors are supported by the following funding: National Institute of Mental Health R01 MH126940 (JRP, TEM), K23 MH112889 (JRP), RF1MH120843 (TEM), R01 MH122446 (TEM), T32 MH019927 (AS), R01 MH119119 (MMM); National Institute on Alcohol Abuse and Alcoholism T32 AA027488 (AGE); German Research Foundation (DFG) SCHM 3732/1-1, 470147139 (KS).
| Funders | Funder number |
|---|---|
| Deutsche Forschungsgemeinschaft | |
| National Institute on Alcohol Abuse and Alcoholism | T32 AA027488 |
| National Institute on Alcohol Abuse and Alcoholism | |
| National Institute of Mental Health | R01 MH119119, R01 MH122446, T32 MH019927, K23 MH112889, R01 MH126940, RF1MH120843 |
| National Institute of Mental Health | |
| California Department of Fish and Game | SCHM 3732/1-1, 470147139 |
| California Department of Fish and Game |
ASJC Scopus subject areas
- Molecular Biology
- Psychiatry and Mental health
- Cellular and Molecular Neuroscience