Women with premenstrual dysphoric disorder have altered sensitivity to allopregnanolone over the menstrual cycle compared to controls—a pilot study
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Abstract
Rationale
In premenstrual dysphoric disorder (PMDD), a condition that afflicts 3–8 % of women in fertile ages, the cyclic recurrence of debilitating mood symptoms is restricted to the luteal phase of the menstrual cycle. The progesterone metabolite allopregnanolone is produced by the corpus luteum, and circulating levels are reflected in the brain. Allopregnanolone is a modulator of the GABAA receptor, enhancing the effect of γ-aminobutyric acid (GABA). Previous studies have demonstrated different sensitivity to other GABAA receptor agonists, i.e., benzodiazepines, alcohol, and pregnanolone, in PMDD patients compared to controls.
Objectives
This study aimed to investigate the sensitivity to intravenous allopregnanolone over the menstrual cycle in PMDD patients.
Methods
Allopregnanolone, 0.05 mg/kg, was administered intravenously once in the mid-follicular and once in the luteal phase of the menstrual cycle to 10 PMDD patients and 10 control subjects. The saccadic eye velocity (SEV) was recorded by electrooculography as a measurement of functional GABAA receptor activity, at baseline and repeatedly after the injection. A mixed model was used to analyze data.
Results
There was a highly significant group × phase interaction in the SEV response to allopregnanolone (F(1,327.489) = 12.747, p < 0.001). In the PMDD group, the SEV response was decreased in the follicular phase compared to the luteal phase (F(1,168) = 7.776, p = 0.006), whereas in the control group, the difference was opposite during the menstrual cycle (F(1,158.45) = 5.70, p = 0.018).
Conclusions
The effect of exogenous allopregnanolone is associated with menstrual cycle phase in PMDD patients and in controls. The results suggest an altered sensitivity to allopregnanolone in PMDD patients.
Keywords
Neurosteroid GABA Premenstrual dysphoric disorder Saccadic eye velocity Menstrual cycleNotes
Acknowledgments
This study was supported by grants from the Swedish Research Council, medicine proj. 4X-11198, Västerbottens läns landsting centrala ALF and Spjutspets and Umeå University foundations. The authors are thankful to Elisabeth Zingmark för excellent laboratory work.
Compliance with ethical standards
Conflict of interest
Torbjörn Bäckström has shares in Umecrine AB. None of the other authors declare any conflicts of interest.
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