SERUM HORMONE CONCENTRATIONS DURING TREATMENT WITH MULTIPLE RISING DOSES OF RECOMBINANT FOLLICLE-STIMULATING-HORMONE (PUREGON-ASTERISK) IN MEN WITH HYPOGONADOTROPIC HYPOGONADISM

Citation
B. Mannaerts et al., SERUM HORMONE CONCENTRATIONS DURING TREATMENT WITH MULTIPLE RISING DOSES OF RECOMBINANT FOLLICLE-STIMULATING-HORMONE (PUREGON-ASTERISK) IN MEN WITH HYPOGONADOTROPIC HYPOGONADISM, Fertility and sterility, 69(2), 1998, pp. 24-27
Citations number
4
Categorie Soggetti
Obsetric & Gynecology
Journal title
ISSN journal
00150282
Volume
69
Issue
2
Year of publication
1998
Supplement
1
Pages
24 - 27
Database
ISI
SICI code
0015-0282(1998)69:2<24:SHCDTW>2.0.ZU;2-H
Abstract
Objective: To study increases of serum FSH and gonadal response in gon adotropin-deficient men treated with recombinant FSH (Puregon; NV Orga non, Oss, the Netherlands). Design: An open, prospective, multiple ris ing dose study in which volunteers received single daily IM doses of r ecombinant FSH for 3 weeks. The dose administered was increased at wee kly intervals: the first 7 days, 75 IU/d; the subsequent 7 days, 150 I U/d; and the last 7 days, 225 IU/d. Participant(s): Nine men suffering from isolated gonadotropin deficiency or panhypopituitarism. Main Out come Measurement(s): Immunoreactive FSH, LH, inhibin, T, and androsten edione. Result(s): Serum immunoreactive FSH (median) rose in accordanc e with the recombinant FSH doses administered from 0.5 mIU/mL (range < 0.05 to 1.9 mIU/mL) at baseline to 4.3 mIU/mL (range 2.0 to 8.5 mIU/mL ), 8.4 mIU/mL (range 4.9 to 17.8 mIU/mL), and 13.6 mIU/mL (5.6 to 28.4 mIU/mL) after 1, 2, and 3 weeks of medication, respectively. The elim ination half-life of recombinant FSH was 48 +/- 5 hours (mean +/- SD), which was slightly longer than that reported after single dose admini stration of recombinant FSH (32 +/- 12 hours). The bioactivity of reco mbinant FSH was reflected by serum inhibin levels, which rose from 116 U/L (range 34 to 356 U/L) at baseline to 350 U/L (range 63 to 1,109 U /L) at day 22. However, serum FSH and inhibin levels did not correlate when compared after 1, 2, and 3 weeks of recombinant FSH administrati on. Serum immunoreactive LH, T, androstenedione, and E-2 were 0.2 mIU/ mL (range <0.05 to 0.7 mIU/mL [conversion factor to SI unit, 1.0]), 58 ng/dL (range <12 to 222 ng/dL [conversion factor to SI unit, 0.0347]) , 14 ng/dL (range 6 to 115 ng/dL [conversion factor to SI unit, 0.0349 ]), and 14 pg/mL (range <14 to 16 pg/mL [conversion factor to SI unit, 3.67]), respectively, at baseline and remained unchanged during the e ntire treatment period. Conclusion(s): These data indicate that recomb inant FSH treatment increases serum FSH in a dose-proportional fashion , increases inhibin secretion, and lacks intrinsic LH activity. (C) 19 96 by American Society for Reproductive Medicine.