Roles of clock genes in the pathogenesis of Parkinson's disease.

Ageing Res Rev

Novel Global Community Educational Foundation, Peterlee Place NSW2700, Australia; AFNP Med, Haidingergasse 29, 1030 Wien, Austria.

Published: February 2022

AI Article Synopsis

  • - Parkinson's disease (PD) is increasingly common in older adults, and recent research indicates that disruptions in circadian rhythms are prevalent among PD patients and may influence the disease's progression.
  • - This review summarizes findings on clock gene expression in both PD patients and animal models, highlighting the potential impact of these genes on PD development and symptoms, along with discussions on epigenetic analyses and gene variants.
  • - Furthermore, the review explores how clock genes affect mitochondrial function and hormone secretion, which could be linked to PD, while also noting the limitations of current studies and suggesting directions for future research.

Article Abstract

Parkinson's disease (PD) is a common motor disorder that has become increasingly prevalent in the ageing population. Recent works have suggested that circadian rhythms disruption is a common event in PD patients. Clock genes regulate the circadian rhythm of biological processes in eukaryotic organisms, but their roles in PD remain unclear. Despite this, several lines of evidence point to the possibility that clock genes may have a significant impact on the development and progression of the disease. This review aims to consolidate recent understanding of the roles of clock genes in PD. We first summarized the findings of clock gene expression and epigenetic analyses in PD patients and animal models. We also discussed the potential contributory role of clock gene variants in the development of PD and/or its symptoms. We further reviewed the mechanisms by which clock genes affect mitochondrial dynamics as well as the rhythmic synthesis and secretion of endocrine hormones, the impairment of which may contribute to the development of PD. Finally, we discussed the limitations of the currently available studies, and suggested future potential studies to deepen our understanding of the roles of clock genes in PD pathogenesis.

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http://dx.doi.org/10.1016/j.arr.2021.101554DOI Listing

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