Abstract

PurposePolycystic ovary syndrome (PCOS) is a common endocrine disorder disease among women in reproductive-age. Since follicle stimulating hormone (FSH) exerts important biological functions, the association between PCOS and FSH receptor (FSHR) polymorphisms attracts wide attention. The aim of this study was to evaluate whether polymorphisms of FSHR at 307 and 680 codons are associated with PCOS patients in China.MethodsPatients with PCOS (n = 215) and controls (n = 205) were recruited from Shanxi Province in north China. They are Han ethnics. Genomic DNA was isolated from the venous blood. The Ala307Thr and Ser680Asn polymorphisms of FSHR were analyzed by polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP) and direct DNA sequencing.ResultsThe distributions of genotype and allele of Ala307Thr and Ser680Asn polymorphisms of FSHR were not statistically different between the PCOS patients and the controls. Analysis of the frequency of FSHR polymorphisms showed no statistical difference among the PCOS patients with different obesity standards. Although there were no statistical differences in the most of the endocrine parameters including LH, LH/FSH, E2, P and T as well as the clinical pregnancy rate, there were significant differences in the levels of FSH and PRL among PCOS patients carrying different genotypes of Ala307Thr and Ser680Asn polymorphisms.ConclusionThe Ala307Thr and Ser680Asn polymorphisms of FSHR are not associated with PCOS in Han ethnic Chinese women in north China. The FSHR polymorphisms was related to the levels of FSH and PRL but not other PCOS-associated endocrine hormones as well as clinical pregnancy rate in PCOS patients of Han Chinese ethnical population.

Highlights

  • Polycystic ovary syndrome (PCOS) is a common endocrine disorder disease among women of reproductive age

  • We found that the association between FSH receptor (FSHR) polymorphisms and PCOS in China was lack of consistency [15, 16]

  • It has been known that PCOS is a hereditary endocrine disease

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Summary

Introduction

Polycystic ovary syndrome (PCOS) is a common endocrine disorder disease among women of reproductive age. The prevalence of PCOS is 5–10 % and the clinical manifestation of the disease is diverse [1]. According to the 2003 Rotterdam criteria [2], the characteristics of PCOS mainly include oligomenorrhea or amenorrhea, hyperandrogenism and polycystic ovary morphology. The pathogenesis of PCOS is not fully understood. The influence of heredity and environment is considered to be the potential causative factors for the disease. Recent studies revealed that there are multiple susceptibility genes associated with PCOS, including growth hormone receptor exon 3 [3], CYP11A1 [4] and GnRH [5]

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