A systematic review of variations in circadian rhythm genes and type 2 diabetes

Nutr Health. 2024 Mar;30(1):61-75. doi: 10.1177/02601060231179777. Epub 2023 Jun 6.

Abstract

Background: Type 2 diabetes is a chronic disease that has severe individual and societal consequences, which is forecast to worsen in the future. A new field of investigation is variations in circadian rhythm genes, in conjunction with diet and sleep variables, associations with, and effects on, type 2 diabetes development.

Objective: This systematic review aimed to analyse all current literature regarding circadian rhythm gene variations and type 2 diabetes, and explore their interplay with diet and sleep variables on type 2 diabetes outcomes. This review was registered with PROSPERO (CRD42021259682).

Methodology: Embase and Pubmed were searched on 6/8/2021/11/8/2021 for studies of all designs, including participants from both sexes, all ethnicities, ages, and geographic locations. Participants with risk alleles/genotypes were compared with the wildtype regarding type 2 diabetes outcomes. Studies risk of bias were scored according to the risk of bias in non-randomised studies - interventions/exposures criteria.

Results: In total, 31 studies were found (association n = 29/intervention n = 2) including >600,000 participants from various ethnicities, sexes, and ages. Variations in the melatonin receptor 1B, brain and muscle arnt-like 1 and period circadian regulator (PER) genes were consistently associated with type 2 diabetes outcomes.

Conclusions: Individuals with variations in melatonin receptor 1B, brain and muscle arnt-like 1 and PER may be at higher risk of type 2 diabetes. Further research is needed regarding other circadian rhythm genes. More longitudinal studies and randomised trials are required before clinical recommendations can be made.

Keywords: Type 2 diabetes; circadian rhythm; diet; genetics; sleep.

Publication types

  • Systematic Review
  • Review

MeSH terms

  • Circadian Rhythm / genetics
  • Diabetes Mellitus, Type 2* / genetics
  • Female
  • Humans
  • Male
  • Melatonin*
  • Receptors, Melatonin
  • Sleep / genetics

Substances

  • Melatonin
  • Receptors, Melatonin