Objective: To study whether weekly low dose of mifepristone (5 mg or 10 mg) is sufficient to prevent pregnancy.
Methods: Thirty-nine women were randomly allocated to take mifepristone 5 mg (group A) or 10 mg (group B) doses once weekly starting on cycle day 2-3. The serum levels of luteinizing hormone (LH) and follicle stimulating hormone (FSH) were determined by enzymeimmunoassay (EIA), and estradiol (E2) and progesterone (P) levels by radioimmunassay (RIA). Serum mifepristone concentrations were measured by high performance liquid chromatography (HPLC). Morphometric analyses and progesterone receptor (PR), Dolichus biflorus agglutinin (DBA-lectin) and integrin alpha v beta 3 of endometrium were also measured.
Results: There were 4 pregnancies out of 64 cycles in group A, and 3 out of 68 cycles in group B. Normal LH and FSH peak could be detected in the first treatment cycles, LH peak appeared on 15-17 d. The concentrations of P were (51.93 +/- 7.91) nmol/lL and (69.00 +/- 21.29) nmol/L in group A and B respectively. The average level of E2 was (407.81 +/- 89.27) pmol/L in group A, and (557.85 +/- 204.69) pmol/L in group B. Serum mifepristone level could be detected within 36 hours. The PR concentration in endometrium decreased significantly, but not of DBA-lectin, integrin alpha v beta 3.
Conclusions: Administration of mifepristone 5 mg or 10 mg once weekly does not inhibit ovulation completely. The follicular phase prolonged slightly, and E2 levels were low following treatment. The endometrium showed delayed development. The clinical contraceptive effectiveness needs to be improved.