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Randomised trial, 2024

Does SPRM treatment change white matter volume in the brain in women with PMDD?

No. The study found no change in white matter volume with treatment, which is a fairly confident finding from a controlled trial, though the sample size was not reported in the abstract.

Moderate study design Women with PMDD (exact number not reported in the abstract)

What they did

Randomized controlled trial where women with PMDD had brain MRI scans before and after 3 months of treatment with either a progesterone-blocking drug (ulipristal acetate) or placebo.

What they found

No white matter volume changes were found in any brain region in either the treatment or placebo group after 3 months. Researchers examined 8 specific white matter pathways but found no differences in any of them.

What it means for you

White matter volume probably does not explain how SPRM drugs help PMDD symptoms. The study had solid design but only examined one specific type of brain structure. It did not look at other types of brain changes that might explain how the drug works.

3 months

Duration of treatment

8

White matter brain regions examined

About the study

Original title
White matter volume and treatment with selective progesterone receptor modulator in patients with premenstrual dysphoric disorder
Authors
Kaltsouni E, Wikström J, Lanzenberger R et al.
Journal
Psychoneuroendocrinology
Year
2024
Study design
Randomised trial
What was tested
Ulipristal acetate (a progesterone-blocking drug) versus placebo for 3 months
Open access
Yes
Original abstract

Premenstrual dysphoric disorder (PMDD) is a mood disorder for which selective progesterone receptor modulator (SPRM) treatment has been demonstrated to be beneficial. The neural signatures of this treatment have been so far identified as greater fronto-cingulate reactivity during aggressive response to provocation, but no changes in terms of gray matter structure. White matter has recently been found to differ between patients with PMDD and healthy controls. The present study thus sought to investigate the relationship between white matter volume and SPRM treatment in patients with PMDD. A pharmaco-neuroimaging study was conducted on patients with PMDD participating in a randomized controlled trial. Participants underwent magnetic resonance imaging before and after treatment randomization to ulipristal acetate (an SPRM), or placebo, for three months. The interaction effect of treatment by time on white matter volume (WMV) was assessed. Voxel based morphometry analyses were performed on both a whole brain exploratory level and on regions of interest. No treatment effect was observed on WMV in any region, including the anterior thalamic radiations, cingulum, forceps minor, fornix, inferior fronto-occipital fasciculus, superior cerebellar peduncle, superior longitudinal fasciculus, and uncinate fasciculus. This is the first finding to indicate that no white matter volume alterations follow three-month progesterone antagonism, suggesting that white matter volume does not participate in symptom relief upon SPRM treatment for PMDD.

Reproduced under CC-BY.

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