Case-control study, 2025
Are brain structure differences in PMDD permanent or temporary?
Brain volume differences in women with PMDD appear to be permanent traits that don't change across the menstrual cycle. This suggests the differences reflect an underlying vulnerability to PMDD rather than temporary changes from symptoms.
What they did
28 women with PMDD and 26 healthy controls had brain scans during two different phases of their menstrual cycle (mid-follicular and late-luteal). Researchers measured the volume of grey matter in different brain regions at each time point.
What they found
Women with PMDD had smaller brain volumes compared to controls across both menstrual cycle phases, particularly in the cerebellum and cuneus. The effect sizes ranged from Cohen's d = 0.4 to 1.1. The brain differences did not change between cycle phases, meaning they were consistent throughout the cycle.
What it means for you
The brain differences in PMDD are stable traits present throughout the menstrual cycle, not just during the symptomatic phase. This suggests the differences may represent a biological vulnerability to developing PMDD. However, the sample was relatively small.
28
Women with PMDD
26
Healthy control women
0.4-1.1
Cohen's d effect size range
About the study
- Original title
- Trait- versus state- grey matter volume alterations in premenstrual dysphoric disorder
- Authors
- Stiernman L, Dubol M, Sundström-Poromaa I et al.
- Journal
- BMC psychiatry
- Year
- 2025
- Study design
- Case-control study
- Participants
- 28
- What was tested
- None; observational study comparing brain scans across menstrual cycle phases
- Open access
- Yes
- Read the paper
- doi.org/10.1186/s12888-025-07533-5
Original abstract
BACKGROUND: Premenstrual dysphoric disorder (PMDD) is characterized by symptoms of irritability, affective lability, anxiety, and depression, which occur only in the luteal phase of ovulatory menstrual cycles. This offers an ideal model to assess the neural correlates of the on and off switch of mood symptoms. Recently, we highlighted differences in grey matter volume between individuals with PMDD and healthy controls during the luteal phase, depicting smaller volumes in those diagnosed with the condition. However, it is unknown whether such alterations represent state-like changes specific to the symptomatic phase, or trait-like characteristics. METHODS: Here, 28 patients with PMDD and 26 controls underwent anatomical magnetic resonance imaging during the mid-follicular and the late-luteal phases of the menstrual cycle. For each time point, we assessed grey matter volumes over the whole brain using voxel-based morphometry. RESULTS: We found no group-by-phase interaction effect on grey matter volumes, but a main effect of group across menstrual cycle phases, suggesting trait rather than state structural markers of PMDD. Patients displayed smaller volumes compared to controls, primarily in the cerebellum and cuneus, and at a trend-level in ventral occipito-temporal, parietal, paracentral and orbitofrontal areas, as well as the putamen (Cohen’s d range: 0.4–1.1). CONCLUSIONS: These findings suggest that the differences in grey matter volumes found in PMDD are stable across the menstrual cycle and could represent trait-like, vulnerability markers of PMDD.
Reproduced under CC-BY.
Topics
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