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Lab study, 2020

Can an estrogen and gene variant cause PMDD-like mood symptoms?

Mice carrying a BDNF gene variant developed anxiety and depression-like behavior when given estrogen, similar to PMDD symptoms.

Early or limited evidence Ovariectomized mice with or without a BDNF gene variant

What they did

Ovariectomized mice with and without a BDNF gene variant were given estradiol in drinking water for 6 weeks or placebo. Researchers tested their anxiety and depression using behavioral tests and measured gene expression in the brain.

What they found

Estradiol caused anxiety-like and depression-like behavior in mice with the gene variant but not in normal mice. Gene expression patterns in the treated mice with the variant matched patterns seen in women with PMDD.

What it means for you

This suggests that a combination of a specific gene variant and estrogen exposure might trigger PMDD-like symptoms. The genes involved control how cells respond to estrogen. The main limit is this is a mouse study, and PMDD affects over 5% of women, so many factors besides this one gene are likely involved.

over 5%

Percentage of women affected by PMDD

6 weeks

Duration of estradiol treatment

About the study

Original title
Epigenetic intersection of BDNF Val66Met genotype with premenstrual dysphoric disorder transcriptome in a cross-species model of estradiol add-back
Authors
Marrocco J, Einhorn NR, Petty GH et al.
Journal
Molecular psychiatry
Year
2020
Study design
Lab study
What was tested
Estradiol in drinking water for 6 weeks
Open access
Yes
Original abstract

Premenstrual dysphoric disorder (PMDD) affects over 5% of women, with symptoms similar to anxiety and major depression, and is associated with differential sensitivity to circulating ovarian hormones. Little is known about the genetic and epigenetic factors that increase the risk to develop PMDD. We report that 17β-estradiol (E2) affects the behavior and the epigenome in a mouse model carrying a single-nucleotide polymorphism of the brain-derived neurotrophic factor gene (BDNF Val66Met), in a way that recapitulates the hallmarks of PMDD. Ovariectomized mice heterozygous for the BDNF Met allele (Het-Met) and their matched wild-type (WT) mice were administered estradiol or vehicle in drinking water for 6 weeks. Using the open field and the splash test, we show that E2 add-back induces anxiety-like and depression-like behavior in Het-Met mice, but not in WT mice. RNA-seq of the ventral hippocampus (vHpc) highlights that E2-dependent gene expression is markedly different between WT mice and Het-Met mice. Through a comparative whole-genome RNA-seq analysis between mouse vHpc and lymphoblastoid cell line cultures from control women and women with PMDD, we discovered common epigenetic biomarkers that transcend species and cell types. Those genes include epigenetic modifiers of the ESC/E(Z) complex, an effector of response to ovarian steroids. Although the BDNF Met genotype intersects the behavioral and transcriptional traits of women with PMDD, we suggest that these similarities speak to the epigenetic factors by which ovarian steroids produce negative behavioral effects.

Reproduced under CC-BY.

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