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Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
Score 2
2020 pubmed 7 citations

Relevance of <i>KISS1</i> gene polymorphisms in susceptibility to polycystic ovary syndrome and its associated endocrine and metabolic disturbances.

Daghestani. M H MH; Daghestani. M H MH; Daghistani. M M; Ambreen. K K; Almuammar. M N MN; Al Neghery. L M LM; Warsy. A S AS

Key Findings

  • Three new KISS1 gene variants were discovered, but only one (rs1213704663C>G) showed a strong link to PCOS
  • The rs1213704663C>G variant’s GG genotype is associated with higher LH and estradiol and a higher LH/FSH ratio in PCOS women
  • The same variant does not affect circulating kisspeptin levels

Practical Outcomes

  • If you’re doing personal genetic testing, spotting the rs1213704663C>G variant could flag a higher risk for PCOS‑related hormone imbalances. It suggests you might want to monitor LH, FSH, and estrogen levels more closely, but there’s no direct dosage or treatment change based on this finding.

Summary

A study found a specific genetic change in the KISS1 gene (rs1213704663C>G) that’s linked to a higher chance of polycystic ovary syndrome (PCOS) and to higher LH and estrogen levels, but it doesn’t change kisspeptin levels. This isn’t a treatment, just a genetic risk marker.

Abstract

<b>Background</b>: Variations in <i>KISS1</i> may be an emerging factor in polycystic ovary syndrome (PCOS) We hypothesised links between <i>KISS1</i> polymorphisms in PCOS and its associated endocrine and metabolic disturbances. <b>Methods</b>: The study included 104 PCOS women and 109 controls. Endocrine (kisspeptin, LH, FSH, LH-FSH ratio, oestradiol) and metabolic (cholesterol, triglycerides, HDL, LDL, insulin and glucose) parameters were measured. PCR and nucleotide sequencing were carried out to screen single nucleotide polymorphisms (SNPs) of <i>KISS1</i>. Endocrine and metabolic parameters of PCOS women were compared in the genotypes. <b>Results</b>: Three novel SNPs (rs1213704663C&gt;G, rs1481572212T&gt;G and rs775770652G&gt;A) were detected in <i>KISS1</i>. Of these SNPs, the genotype and allele frequencies of rs1213704663C&gt;G were all significantly associated p&lt;0.001 with PCOS. The LH and oestradiol hypersecretion, and increased LH-FSH ratio of PCOS women were significantly influenced by the GG genotype of rs1213704663, but, this SNP did not influence kisspeptin levels. The other two SNPs rs1481572212T&gt;G and rs775770652G&gt;A exhibited no clinical significance. <b>Conclusion</b>: rs1213704663C&gt;G variation in <i>KISS1</i> is linked to PCOS and its associated endocrine and metabolic disturbances (LH and oestradiol hypersecretion, and increased LH/FSH).

Study Information

Provider

pubmed

Year

2020

Date

2020-06-08T00:00:00.000Z

DOI

10.1080/09674845.2020.1726662

Citations

7

References

32