Serum klotho as a novel biomarker for metabolic syndrome: findings from a large national cohort

Front Endocrinol (Lausanne). 2024 Mar 4:15:1295927. doi: 10.3389/fendo.2024.1295927. eCollection 2024.

Abstract

Background: Metabolic syndrome is a cluster of metabolic abnormalities that significantly increase the risk of cardiovascular disease and mortality. The identification of novel biomarkers associated with mortality in patients with metabolic syndrome could facilitate early risk stratification and targeted interventions.

Methods: We conducted a large prospective cohort study using data from five cycles (2009-2016) of the National Health and Nutrition Examination Survey (NHANES) database, including a total of 40,439 participants. Logistic regression analysis was used to assess the association between serum klotho protein levels and metabolic syndrome, while Cox regression analysis was employed to examine the correlation between serum klotho levels and all-cause mortality. Mortality data were updated until December 31, 2019.

Results: After adjusting for demographic and socioeconomic confounders, the logistic regression model demonstrated that higher serum klotho levels were significantly associated with a decreased prevalence of metabolic syndrome (OR [95% CI] Highest vs. lowest quartile: 0.84 [0.70-0.99], P=0.038). In the Cox regression model, elevated klotho levels were found to significantly reduce the risk of all-cause mortality among individuals with metabolic syndrome (HR [95% CI] Highest vs. lowest quartile: 0.68 [0.51-0.90], P=0.006).

Conclusion: Serum klotho levels were found to be inversely associated with the prevalence of metabolic syndrome, independent of potential confounding factors such as demographics, socioeconomic status, and lifestyle factors. Furthermore, higher klotho levels strongly indicated a lower risk of all-cause mortality in individuals with metabolic syndrome.

Keywords: NHANES; biomarkers; klotho; metabolic syndrome; mortality.

MeSH terms

  • Biomarkers
  • Humans
  • Metabolic Syndrome* / diagnosis
  • Metabolic Syndrome* / epidemiology
  • Nutrition Surveys
  • Prospective Studies
  • Risk Factors

Substances

  • Biomarkers
  • KL protein, human

Grants and funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.