We found a match
Your institution may have access to this item. Find your institution then sign in to continue.
- Title
CAG repeat length in the androgen receptor gene and gonadotrophin suppression influence the effectiveness of hormonal male contraception.
- Authors
Eckardstein, Sigrid v.; Schmidt, Anja; Kamischke, Axel; Simoni, Manuela; Gromoll, Jörg; Nieschlag, Eberhard
- Abstract
Summary objective Nonuniformity in suppression of spermatogenesis induced by various hormones or hormone combinations has impeded the development of an effective hormonal male contraceptive. The basis for this heterogeneity in response remained unresolved to date; however, the presence of ethnic differences points to an involvement of genetic factors. patients and measurements In a retrospective analysis we investigated the impact of a CAG repeat polymorphism in the androgen receptor and polymorphic sites in the oestrogen and FSH receptor genes on spermatogenic suppression in 85 Caucasian men treated with different regimens of hormonal contraception. results Failure to reduce sperm concentrations below 3 million/ml was significantly associated with insufficient suppression of gonadotrophins. The extent of gonadotrophin suppression was not explained by any polymorphism but was primarily pharmacological, resulting from addition of gestagens to testosterone. When LH and FSH suppression was rapid and persistent none of the polymorphisms studied explained why some men failed to achieve azoospermia. In cases with incomplete gonadotrophin suppression the chances of becoming azoospermic were 2·5 times higher in men having more than 22 CAG repeats. conclusions In summary, our analysis shows that in a subset of men, effective hormonal male contraception can be achieved even in the absence of complete gonadotrophin suppression.
- Subjects
MALE contraception; REGULATION of spermatogenesis; GONADOTROPIN
- Publication
Clinical Endocrinology, 2002, Vol 57, Issue 5, p647
- ISSN
0300-0664
- Publication type
Article
- DOI
10.1046/j.1365-2265.2002.01652.x