CYP1A1 and GSTM1 genes polymorphism and its association with endometriosis : A pilot study

Shikha Sachan, Rohini R. Nair, Anuradha Khanna, Kiran Singh
In: Asian Pacific Journal of Reproduction · 2013 · vol. 2(4) , pp. 297–300 · doi:10.1016/s2305-0500(13)60165-7 · W2082683471
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⚙ AI-generated summary by claude@2026-06, 2026-06-06 ⓘ

This pilot study investigated CYP1A1 and GSTM1 gene polymorphisms in relation to endometriosis, finding GSTM1 null genotype and CYP1A1 C allele are associated with increased risk in the North Indian population.

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Abstract

To study the genetic association between Cytochrome P450 family 1 (CYP1A1) T6235C polymorphism and glutathione S-transferase M1 (GSTM1) null mutations and endometriosis. A total of 121 unrelated women having complaints of pelvic pain, dysmenorrhea, dysuria, dyschezia, dysparenuia and infertility were enrolled. Out of these 71 consented for laparoscopy, 66 were diagnosed as endometriosis as per operative. Genomic DNA isolated from endometriosis patients and controls were subjected to polymerase chain reactions to determine the GSTM1 null genotypes whereas polymorphism of CYP1A1 T6235C was determined through PCR-RFLP. The GSTM1 null genotype was found to be associated with endometriosis however there was no significant difference in the frequencies of the CYP1A1 6235 CC genotype between endometriosis patients and controls. The homozygous mutant and allele frequency of CYP1A1 T6235C differed significantly between patients having endometriosis and healthy control. The data of the present study clearly suggests that GSTM1 null allele and CYP1A1 C allele is a genetic risk factor for endometriosis in North Indian population.

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endometriosisdysmenorrheainfertility

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