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DOI 10.1016/j.ejogrb.2015.11.002

Медицинская библиотека · European journal of obstetrics, gynecology, and reproductive biology · 2015

Analysis of Connexin37 gene C1019T polymorphism and PCOS susceptibility in South Indian population: case-control study.

Guruvaiah Praveen, Govatati Suresh, Reddy Tumu Venkat, Beeram Himabindu, Deenadayal Mamata, Shivaji Sisinthy, Bhanoori Manjula

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

Polycystic ovarian syndrome (PCOS) is a complex and multifactorial disorder believed to be the consequence of a complex interaction between genetic, immunological, and environmental factors. The main aim of this study was to investigate the association of Connexin37 (Cx37)/Gap junction alpha 4 (GJA4) gene C1019T single nucleotide polymorphism (SNP) with the susceptibility to polycystic ovarian syndrome (PCOS) in South Indian women.

STUDY

DESIGN

This study comprises 98 PCOS patients and 100 healthy women without PCOS of South Indian origin. We genotyped total of seventeen selected Cx37 SNPs including C1019T (rs1764391) by polymerase chain reaction and sequencing analysis. The genotype frequency and allele distributions of cases and controls were analyzed using Fisher's exact test.

RESULTS

The genotype and allele frequencies of the C1019T polymorphism significantly differ between cases and controls. The frequencies of C/C genotype (P=0.009) and 'C' allele (P=0.002) of the C1019T polymorphism showed a significant prevalence in cases compared to controls.

CONCLUSION

Our findings suggest that the Cx37 C1019T variation may contribute to the risk of PCOS in the South Indian women.

Для цитирования: Guruvaiah Praveen, Govatati Suresh, Reddy Tumu Venkat, Beeram Himabindu, Deenadayal Mamata, Shivaji Sisinthy, Bhanoori Manjula. Analysis of Connexin37 gene C1019T polymorphism and PCOS susceptibility in South Indian population: case-control study.. European journal of obstetrics, gynecology, and reproductive biology. 2015. DOI: 10.1016/j.ejogrb.2015.11.002.

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