Background The symptoms of women with premenstrual syndromeimprove in response to suppression of ovarian function, althoughthese women have no evidence of ovarian dysfunction. We undertooka study to determine the role of estrogen and progesterone inthis syndrome.
Methods We first studied the effect of ovarian suppression withleuprolide, an agonist analogue of gonadotropin-releasing hormone,or placebo on symptoms in 20 women with premenstrual syndrome.Ten women whose symptoms improved during leuprolide treatmentwere given estradiol and progesterone in a double-blind, crossoverdesign, each for four weeks, during continued leuprolide administration.Women without premenstrual syndrome (normal women) participatedin a similar protocol. Outcomes were assessed on the basis ofdaily self-reports by the patients and biweekly rater-administeredsymptom-rating scales.
Results The 10 women with premenstrual syndrome who were givenleuprolide had a significant decrease in symptoms as comparedwith base-line values and with values for the 10 women who weregiven placebo. The 10 women with premenstrual syndrome who weregiven leuprolide plus estradiol or progesterone had a significantrecurrence of symptoms, but no changes in mood occurred in 15normal women who received the same regimen or in 5 women withpremenstrual syndrome who were given placebo hormone duringcontinued leuprolide administration.
Conclusions In women with premenstrual syndrome, the occurrenceof symptoms represents an abnormal response to normal hormonalchanges.
Source Information
From the Behavioral Endocrinology Branch, National Institute of Mental Health (P.J.S., L.F.A., D.R.R.); the Developmental Endocrinology Branch, National Institute of Child Health and Human Development (L.K.N.); and the Clinical Center Nursing Department (M.A.D.) all at the National Institutes of Health in Bethesda, Md.
Address reprint requests to Dr. Schmidt at the National Institute of Mental Health, Bldg. 10, Rm. 3N238, 10 Center Dr. MSC 1276, Bethesda, MD 20892-1276.
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