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Dynamics of Suppression and Recovery of Plasma FSH, LH, Androstenedione and Testosterone in Polycystic Ovarian Disease Using an Oral Contraceptive
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1974
Year
Plasma FshHormonal ContraceptiveFertilityOral ContraceptiveReproductive HealthGynecologyPolycystic Ovary SyndromeFemale Reproductive FunctionOvarian AgingOvarian CancerReproductive EndocrinologyFemale InfertilityReproductive MedicineWomen's PhysiologyPublic HealthReproductive HormoneMenopause Hormone TherapyInfertilityProbable Polycystic OvariesLast WeekHormonal Male ContraceptionEndocrinologyPharmacologyOvarian HormoneUterine ReceptivityMenopauseMedicineEndocrine ResearchWomen's HealthSuppression Test
Four women with proven and 3 with probable polycystic ovaries (PCO) had plasma FSH, LH, androstenedione (A) and testosterone (T) measured by radioimmunoassay before and during the administration of norethindrone 2 mg–mestranol 0.1 mg (Ortho-Novum 2 mg) daily for 17–21 days to determine how long a progestin–estrogen preparation should be given to evaluate the degree of suppressibility of elevated peripheral plasma concentrations of A and T in women with PCO. The pattern of recovery of these hormones was also studied. Pretreatment means ± se were: FSH 6.4 ± 1.2 mIU/ml, LH 21 ± 3 mIU/ml, A 515 ± 24 ng/100 ml, T 93 ± 17 ng/100 ml. The mean of each hormone decreased progressively from days 5–8 to days 13–16 of treatment. The mean of each hormone at the 13–16-day treatment period was: FSH 2.7 ± 1.2 mIU/ml, LH 6.7 (5–8) mIU/ml, A 216 ± 21 ng/100 ml and T 33 ± 3 ng/100 ml. Suppression and recovery of A and T were significantly correlated with LH. FSH began recovery before LH, A or T and was not significantly correlated with LH during suppression or recovery. The data established the effectiveness of this pill in correcting the hyperandrogenism associated with PCO and indicate that a suppression test should consist of giving the pill for at least 3 weeks and measuring plasma A and T during the last week of drug administration.