Serum levels of kisspeptin are elevated in critically ill patients

PLoS One. 2018 Oct 17;13(10):e0206064. doi: 10.1371/journal.pone.0206064. eCollection 2018.

Abstract

Introduction: Members of the adipokine family such as resistin, adiponectin and omentin have recently been described as novel biomarkers with a diagnostic and prognostic role in the context of critically ill patients during intensive care unit (ICU) treatment. Kisspeptin represent another member of this family and has been shown to be closely correlated to different members of the adipokine family in manifold diseases. However, its role in critical illness and sepsis is currently unknown.

Materials and methods: Kisspeptin serum concentrations were measured in 133 ICU patients admitted to the medical ICU. Results were compared with 36 healthy controls.

Results: Kisspeptin serum levels were elevated in the serum of critically ill patients at admission to the ICU, when compared to healthy controls, and remained increased after 72 hours of ICU treatment. Notably, kisspeptin levels were independent of the presence of sepsis and etiology of critical illness. In line, serum concentrations of kisspeptin were not correlated to concentrations of inflammatory cytokines or established sepsis markers. Serum kisspeptin correlated inversely with the glomerular filtration rate. In contrast to the reported role of other members of the adipokine family, serum levels of kisspeptin were neither predictive for short term survival during ICU treatment nor for patients' overall survival. Kisspeptin levels did not correlate with other adipokines measured in serum, including leptin, resistin, ghrelin, or adiponectin.

Conclusions: Although circulating kisspeptin levels were strongly elevated in ICU-patients, elevated kisspeptin levels were not predictive for an impaired patients' survival.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • Critical Illness*
  • Female
  • Humans
  • Intensive Care Units
  • Kidney / injuries
  • Kidney / pathology
  • Kisspeptins / blood*
  • Male
  • Middle Aged
  • Renal Replacement Therapy
  • Sepsis / blood
  • Survival Analysis
  • Young Adult

Substances

  • Biomarkers
  • Kisspeptins

Grants and funding

This work was supported by project grants from the German Research Foundation (DFG RO 4317/4-1; SFB-TRR57 / P06) and a START grant from the medical faculty RWTH Aachen to C.R. and S.R. as well as a project grant of the German Center for Cardiovascular Disease (DZHK, B18-005Ext) to M.L., M.S. and C.R.