Association analysis of KISS1 polymorphisms and haplotypes with polycystic ovary syndrome

Br J Biomed Sci. 2021 Oct;78(4):201-205. doi: 10.1080/09674845.2020.1864109. Epub 2021 Jan 22.

Abstract

Introduction: KISS1 play an essential role in human reproductive functions by regulating the hypothalamic-pituitary-gonadal axis. Loss-of-function mutations in this gene have been frequently identified in patients with different reproductive disorders. We hypothesised links between KISS1 polymorphisms and polycystic ovary syndrome (PCOS).

Materials and methods: In order to find links between KISS1 polymorphisms rs4889 C > G, rs12998 G > A, and rs35431622 A > G with PCOS, 770 blood samples were obtained from 385 control and 385 PCOS women. DNA was extracted, and genotyped for KISS1 variants by PCR.

Results: rs12998 G > A was linked to PCOS in dominant (p < 0.001), recessive (p < 0.001), co-dominant (p < 0.001), and allelic models (p < 0.001). In addition, rs4889 C > G was linked in recessive, dominant, co-dominant, and allelic models (p < 0.001). rs35431622 A > G was not linked to PCOS. Further analysis indicated that C-G-G haplotype was more common and G-A-G haplotype was less prevalent in cases compared with controls.

Conclusion: KISS1 variants rs12998 G > A and rs4889 C > G may be linked to the pathophysiology of PCOS.

Keywords: Polycystic ovary syndrome; kiss1 gene; polymorphism.

MeSH terms

  • Alleles
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease
  • Haplotypes
  • Humans
  • Kisspeptins* / genetics
  • Polycystic Ovary Syndrome* / genetics
  • Polymorphism, Single Nucleotide

Substances

  • KISS1 protein, human
  • Kisspeptins