Abstract
Objective
Endometriosis is an immune-related, chronic inflammatory disease with polygenic predisposition. Cell adhesion molecules are expressed in endometriotic lesions, and in cells and tissues that are involved in the development and progression of the disease. In this study, we investigated the possible association between endometriosis and the G241R and K469E polymorphisms in the intercellular adhesion molecule-1 (ICAM-l) gene in a fapanese population.
Methods
We compared the distribution of the G241R and K469E polymorphisms in the ICAM-l gene in 126 endometriosis patients and 172 controls using polymerase chain reaction—restriction fragment length polymorphism (PCR-RFLP) analysis in a fapanese population.
Results
There were no significant differences between the cases and controls in the allele frequencies or genotype distributions of either the G241R or K469E polymorphisms in the ICAM-l gene. The endometriosis patients were divided into a subgroup of women with severe disease only. However, no significant differences were observed in the allele frequencies and genotype distributions of the ICAM-1 K469E polymorphisms between this subgroup and the controls. In contrast, only one in 169 controls was heterozygous (G/A genotype), and the A allele in the G2 41R polymorphism was not found in any of the 126 endometriosis patients.
Conclusion
Our findings suggest that the G241R and K469E polymorphisms in the ICAM-1 gene are unlikely to be associated with an increased risk of endometriosis in the fapanese population.
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This work was supported by a Grant-in-Aid for Scientific Research 05390506 from the Japanese Ministry of Education, Science and Culture and the Japan Association of Obstetricians and Gynecologists Ogyaa-Donation Foundation (JODF).
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Yamashita, M., Yoshida, S., Kennedy, S. et al. Association Study of Endometriosis and Intercellular Adhesion Molecule-1 (ICAM-1) Gene Polymorphisms in a Japanese Population. Reprod. Sci. 12, 267–271 (2005). https://doi.org/10.1016/j.jsgi.2005.03.002
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DOI: https://doi.org/10.1016/j.jsgi.2005.03.002