Results
PMID | 12042273 |
Gene Name | LHB |
Condition | Endometriosis |
Association |
Associated |
Population size | 230 |
Population details | 230 (85 women with endometriosis, 145 women without endometriosis) |
Sex | Female |
Associated genes | LH |
Other associated phenotypes |
Endometriosis |
Hum Reprod. 2002 Jun;17(6):1532-4. Gazvani, R| Pakarinen, P| Fowler, P| Logan, S| Huhtaniemi, I Department of Obstetrics and Gynaecology, University of Aberdeen, Aberdeen Maternity Hospital, Foresterhill, Aberdeen AB25 2ZD, UK. R.Gazvani@lwh-tr.nwest.nhs.uk BACKGROUND: Subfertile women with endometriosis have been reported to demonstrate impaired follicular growth, ovulatory dysfunction and disturbed LH patterns. In addition, abnormal LH and/or LH receptors have been linked with endometriosis-associated infertility. Carriers of a variant of the beta-subunit of luteinizing hormone (V-LH) are largely healthy; however, differences in their gonadal function such as alterations in gonadal steroidogenesis, ovarian reserve, pubertal development and predisposition to diseases such as infertility and polycystic ovarian disease have been found. METHODS AND RESULTS: To explore the possible relationship between endometriosis and V-LH, we examined its frequency in 230 women undergoing laparoscopic surgery for the investigation of infertility. For the entire study population, 185 (80.4%) were wild type; 42 (18.3%) were heterozygous; and three (1.3%) were homozygous for V-LH. No difference was found between women with (n = 85) and without (n = 145) endometriosis concerning the frequency of the type of LH. CONCLUSION: Our results do not support the hypothesis that the variant form of LH is associated with an altered risk of endometriosis in the population tested. Mesh Terms: Adult| Endometriosis/etiology/*genetics/*immunology| Female| Gene Frequency| *Genetic Variation| Heterozygote| Homozygote| Humans| Infertility, Female/etiology/genetics/immunology| Luteinizing Hormone, beta Subunit/*genetics/*immunology/physiolog |