Emerging role of α-Klotho in energy metabolism and cardiometabolic diseases

Diabetes Metab Syndr. 2023 Oct;17(10):102854. doi: 10.1016/j.dsx.2023.102854. Epub 2023 Sep 14.

Abstract

Background and aim: Klotho was first identified as a gene associated with aging and longevity in 1997. α-Klotho is an anti-aging protein and its role in energy metabolism, various cardiovascular diseases (CVDs), and metabolic disorders is increasingly being recognized. In this review, we aimed to outline the potential protective role and therapeutic prospects of α-Klotho in energy metabolism and cardiometabolic diseases (CMDs).

Methods: We comprehensively reviewed the relevant literature in PubMed using the keywords 'Klotho', 'metabolism', 'cardiovascular', 'diabetes', 'obesity', 'metabolic syndrome', and 'nonalcoholic fatty liver disease'.

Results: α-Klotho can be divided into membrane-bound Klotho, secreted Klotho, and the most studied circulating soluble Klotho that can act as a hormone. Klotho gene polymorphisms have been implicated in energy metabolism and CMDs. α-Klotho can inhibit insulin/insulin growth factor-1 signaling and its overexpression can lead to a 'healthy insulin resistance' and may exert beneficial effects on the regulation of glycolipid metabolism and central energy homeostasis. α-Klotho, mainly serum Klotho, has been revealed to be protective against CVDs, diabetes and its complications, obesity, and nonalcoholic fatty liver disease. Human recombinant Klotho protein/Klotho gene delivery, multiple drugs, or natural products, and exercise can increase α-Klotho expression.

Conclusion: Overall, α-Klotho has demonstrated its potential as a promising target for modulating energy metabolism and CMDs, and further research is needed to explore its utilization in clinical practice in the future.

Keywords: Cardiovascular disease; Energy metabolism; Klotho; Metabolic disorder; α-Klotho.

Publication types

  • Review

MeSH terms

  • Aging / metabolism
  • Cardiovascular Diseases* / etiology
  • Cardiovascular Diseases* / prevention & control
  • Energy Metabolism
  • Glucuronidase* / genetics
  • Glucuronidase* / metabolism
  • Humans
  • Insulin / metabolism
  • Obesity

Substances

  • Glucuronidase
  • Insulin