AI Article Synopsis

  • Polycystic ovary syndrome (PCOS) is a common hormonal disorder affecting women, and the study investigated the relationship between the CYP19 gene and PCOS in Karnataka, India.
  • The research involved 300 women (150 with PCOS and 150 controls), using various genetic and hormonal tests to explore the connection between the CYP19 gene variant (rs2414096) and hormonal levels.
  • Findings revealed that the GG genotype was more prevalent in PCOS patients, but the CYP19 variant itself was not significantly linked to PCOS, although the GG genotype might result in lower aromatase activity, leading to increased androgen levels.

Article Abstract

Background: Polycystic ovary syndrome is a common multifactorial endocrinopathy disorder affecting 5-15% of reproductive women worldwide. The CYP19 gene encodes key enzyme aromatase involved in androgen-to-estrogen conversion which plays a crucial role in the pathophysiology of the syndrome. Very few studies have been done in the Indian population; hence, we investigated whether CYP19 gene rs2414096 SNP is associated with PCOS and hyperandrogenism susceptibility in Karnataka women.

Methods: Three-hundred subjects including 150 PCOS and 150 age-matched controls were involved in the current case-control study. Sex hormones and biochemical estimation were performed by ELISA. Sanger sequencing and PCR-RFLP were used to genotype the SNP rs2414096. Genotypic-phenotypic association was studied. Statistical analysis was performed.

Results: The GG genotype was more common in patients, while the GA genotype was more common in control women. LH/FSH was significantly increased in GG genotype in PCOS when compared with AA and GA genotypes. Variations of CYP19 rs2414096 were not statistically significant with PCOS.

Conclusion: CYP19 rs2414096 polymorphism was not associated with PCOS; however, the homozygous wild GG genotype may exhibit reduced aromatase activity with subsequent hyperandrogenism implicating endocrine abnormalities.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441965PMC
http://dx.doi.org/10.1186/s43141-023-00540-7DOI Listing

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