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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
2020 pubmed

Plasma kisspeptin levels in boys with hypogonadotropic delayed puberty.

Nikitina. Irina L IL; Yukhlina. Yulia N YN; Vasilieva. Elena Y EY; Nagornaya. Irena I II; Grineva. Elena N EN; Kelmanson. Igor A IA

Key Findings

  • Boys with hypogonadotropic delayed puberty had significantly higher plasma kisspeptin (median 45.0 pg/mL) than normal pubertal or pre‑pubertal boys (median 13.8 pg/mL).
  • A kisspeptin level above 16.9 pg/mL predicted delayed puberty with 72.7% sensitivity and 92.0% specificity.
  • Kisspeptin levels did not differ between delayed‑puberty boys who responded or did not respond to a Triptorelin stimulation test.

Practical Outcomes

  • For biohackers and self‑experimenters, this research does not provide actionable guidance on using kisspeptin for performance, longevity, or metabolic health. It is primarily a diagnostic insight for a specific pediatric endocrine disorder, so it has little direct relevance to everyday self‑optimization protocols.

Summary

The study measured kisspeptin levels in the blood of teenage boys with delayed puberty caused by low hormone production, comparing them to normal teens and younger pre‑pubertal boys. It found that boys with this type of delayed puberty had higher kisspeptin levels, and a cutoff value could help diagnose the condition.

Abstract

In hypogonadotropic forms of delayed puberty (DP), hypophyseal follicle-stimulating (FSH) and luteinizing (LH) hormones, normally released with GnRH stimulation, are detected low. Since kisspeptin (KP) is a strong stimulant of GnRH neurons, it is considered to have a role in DP etiology. It may be hypothesized that abnormal plasma levels of KP are indicative of DP. The study aimed at evaluation and comparison of plasma KP levels in boys of pre-pubertal age, with normal puberty and diagnosed primary hypogonadotropic forms of DP. The study comprised 22 boys with verified hypogonadotropic DP (age 14-17 years), 25 boys with normal puberty (age 14-17 years), and 28 pre-pubertal boys (age 6-9 years). Triprorelin stimulation test was performed in DP patients. Plasma KP values were compared between three groups. Statistically significant difference was found for the overall distribution of the plasma KP values across different groups (Kruskal-Wallis H=21.95, P<0.001). The highest values were found in the DP group (median: 45.0 pg/mL). Median values in the pre-pubertal boys and in the normal pubertal adolescents were equal to 13.8 pg/mL. No statistically significant difference was found for plasma KP levels in the DP boys who had either positive or negative response to Triptorelin stimulation test. Plasma KP level exceeding 16.9 pg/mL was a reliable predictor of hypoganadotropic DP (sensitivity 72.7%, specificity 92.0%). Plasma KP levels are elevated in hypogonadotropic DP cases and may serve as a useful diagnostic tool in evaluating boys with DP.

Study Information

Provider

pubmed

Year

2020

Date

2020-01-24T00:00:00.000Z

DOI

10.23736/s0391-1977.20.03101-6