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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 3
2015 pubmed 132 citations

Efficacy of Kisspeptin-54 to Trigger Oocyte Maturation in Women at High Risk of Ovarian Hyperstimulation Syndrome (OHSS) During In Vitro Fertilization (IVF) Therapy.

Abbara. Ali A; Jayasena. Channa N CN; Christopoulos. Georgios G; Narayanaswamy. Shakunthala S; Izzi-Engbeaya. Chioma C; Nijher. Gurjinder M K GM; Comninos. Alexander N AN; Peters. Deborah D; Buckley. Adam A; Ratnasabapathy. Risheka R; Prague. Julia K JK; Salim. Rehan R; Lavery. Stuart A SA; Bloom. Stephen R SR; Szigeti. Matyas M; Ashby. Deborah A DA; Trew. Geoffrey H GH; Dhillo. Waljit S WS

Key Findings

  • Kisspeptin‑54 induced oocyte maturation in 95% of women at high OHSS risk
  • The highest oocyte yield (121%) was seen at 12.8 nmol/kg, outperforming lower doses
  • No moderate, severe, or critical OHSS occurred, and pregnancy/live‑birth rates were good, especially at 9.6 nmol/kg

Practical Outcomes

  • Kisspeptin‑54 could replace traditional triggers like hCG in IVF protocols to lower OHSS risk, with doses around 9.6–12.8 nmol/kg showing the best results. Implementation requires a medical setting and professional monitoring, so it’s not a DIY option but offers a safer clinical pathway for fertility treatments.

Summary

A clinical trial showed that a single injection of kisspeptin‑54 can safely trigger egg maturation in women undergoing IVF who are at high risk for a dangerous condition called ovarian hyperstimulation syndrome (OHSS). The drug worked in 95% of participants, gave the best egg‑retrieval numbers at the highest dose, and led to solid pregnancy and live‑birth rates without any cases of moderate or severe OHSS.

Abstract

In vitro fertilization (IVF) treatment is an effective therapy for infertility, but can result in the potentially life-threatening complication, ovarian hyperstimulation syndrome (OHSS). This study aimed to investigate whether kisspeptin-54 can be used to effectively and safely trigger oocyte maturation in women undergoing IVF treatment at high risk of developing OHSS. This was a phase 2, multi-dose, open-label, randomized clinical trial of 60 women at high risk of developing OHSS carried out during 2013-2014 at Hammersmith Hospital IVF unit, London, United Kingdom. Following a standard recombinant FSH/GnRH antagonist protocol, patients were randomly assigned to receive a single injection of kisspeptin-54 to trigger oocyte maturation using an adaptive design for dose allocation (3.2 nmol/kg, n = 5; 6.4 nmol/kg, n = 20; 9.6 nmol/kg, n = 15; 12.8 nmol/kg, n = 20). Oocytes were retrieved 36 h after kisspeptin-54 administration, assessed for maturation, and fertilized by intracytoplasmic sperm injection with subsequent transfer of one or two embryos. Women were routinely screened for the development of OHSS. Oocyte maturation was measured by oocyte yield (percentage of mature oocytes retrieved from follicles ≥ 14 mm on ultrasound). Secondary outcomes include rates of OHSS and pregnancy. Oocyte maturation occurred in 95% of women. Highest oocyte yield (121%) was observed following 12.8 nmol/kg kisspeptin-54, which was +69% (confidence interval, -16-153%) greater than following 3.2 nmol/kg. At all doses of kisspeptin-54, biochemical pregnancy, clinical pregnancy, and live birth rates per transfer (n = 51) were 63, 53, and 45%, respectively. Highest pregnancy rates were observed following 9.6 nmol/kg kisspeptin-54 (85, 77, and 62%, respectively). No woman developed moderate, severe, or critical OHSS. Kisspeptin-54 is a promising approach to effectively and safely trigger oocyte maturation in women undergoing IVF treatment at high risk of developing OHSS.

Study Information

Provider

pubmed

Year

2015

Date

2015-07-20T00:00:00.000Z

DOI

10.1210/jc.2015-2332

Citations

132

References

29