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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 1
2006 pubmed

Plasma kisspeptin is raised in patients with gestational trophoblastic neoplasia and falls during treatment.

Dhillo. Waljit S WS; Savage. Philip P; Murphy. Kevin G KG; Chaudhri. Owais B OB; Patterson. Michael M; Nijher. Gurjinder M GM; Foggo. Vanessa M VM; Dancey. Garin S GS; Mitchell. Hugh H; Seckl. Michael J MJ; Ghatei. Mohammad A MA; Bloom. Stephen R SR

Key Findings

  • Non‑pregnant women have almost no detectable kisspeptin (<2 pmol/l).
  • Pregnant women show a huge rise in kisspeptin (≈800 pmol/l in the first trimester, ≈2,500 pmol/l in the third trimester).
  • Patients with malignant GTN have elevated kisspeptin (~1,363 pmol/l) that falls to <2 pmol/l after successful chemotherapy, tightly correlating with hCG levels.

Practical Outcomes

  • For biohackers, the main takeaway is that kisspeptin isn’t a useful supplement or biomarker for general longevity, metabolism, or performance. Its relevance is limited to monitoring a rare pregnancy‑related cancer, so it doesn’t inform everyday health protocols.

Summary

The study shows that the hormone‑like peptide kisspeptin spikes a lot during pregnancy and is also high in a rare placental cancer called gestational trophoblastic neoplasia (GTN), then drops back to almost zero after chemotherapy, matching changes in the pregnancy hormone hCG. This mainly tells doctors that kisspeptin could be used to track this specific cancer, but it doesn’t give everyday health or performance advice for most people.

Abstract

Kisspeptin is a 54-amino acid peptide, encoded by the anti-metastasis gene KiSS-1, that activates G protein-coupled receptor 54 (GPR54). The kisspeptin-GPR54 system is critical to normal reproductive development. KiSS-1 gene expression is increased in the human placenta in normal and molar pregnancies. Circulating kisspeptin is dramatically increased in normal pregnancy, but levels in GTN have not previously been reported. The present study was designed to determine whether plasma kisspeptin levels are altered in patients with malignant GTN. Thirty-nine blood samples were taken from 11 patients with malignant GTN at presentation during and after chemotherapy. Blood was also sampled from nonpregnant and pregnant volunteers. Plasma kisspeptin IR and hCG concentrations were measured. Plasma kisspeptin IR concentration in nonpregnant (n = 16) females was &lt;2 pmol/l. Plasma kisspeptin IR in females was 803 +/- 125 pmol/l in the first trimester of pregnancy (n = 13), 2,483 +/- 302 pmol/l in the third trimester of pregnancy (n = 7), and &lt;2 pmol/l on day 15 postpartum (n = 7). Plasma kisspeptin IR and hCG concentrations in patients with malignant GTN were elevated at presentation and fell during and after treatment with chemotherapy in each patient (mean plasma kisspeptin IR: prechemotherapy 1,363 +/- 1,076 pmol/l vs. post-chemotherapy &lt;2 pmol/l, P &lt; 0.0001; mean plasma hCG: prechemotherapy 227,191 +/- 152,354 U/l vs. postchemotherapy 2 U/l, P &lt; 0.0001). Plasma kisspeptin IR strongly positively correlated with plasma hCG levels (r(2) = 0.99, P &lt; 0.0001). Our results suggest that measurement of plasma kisspeptin IR may be a novel tumor marker in patients with malignant GTN.

Study Information

Provider

pubmed

Year

2006

Date

2006-06-06T00:00:00.000Z

DOI

10.1152/ajpendo.00555.2005