AI Article Synopsis

  • Parkinson's disease (PD) is a prevalent neurodegenerative disorder primarily affecting the elderly, leading to significant movement difficulties due to reduced dopamine levels in the brain.
  • * One major challenge in managing PD is the absence of specific early diagnostic biomarkers and effective treatments that can slow down the degeneration of dopaminergic neurons.
  • * This article discusses the role of microRNAs (miRNAs) as epigenetic regulators that contribute to mitochondrial dysfunction in PD and explores their potential as both diagnostic tools and therapeutic targets.

Article Abstract

Parkinson's disease (PD) is the second most common neurodegenerative disease, affecting the elderly worldwide and causing significant movement impairments. The goal of PD treatment is to restore dopamine levels in the striatum and regulate movement symptoms. The lack of specific biomarkers for early diagnosis, as well as medication aimed at addressing the pathogenic mechanisms to decelerate the progression of dopaminergic neurodegeneration, are key roadblocks in the management of PD. Various pathogenic processes have been identified to be involved in the progression of PD, with mitochondrial dysfunction being a major contributor to the disease's pathogenesis. The regulation of mitochondrial functions is influenced by a variety of factors, including epigenetics. microRNAs (miRNAs) are epigenetic modulators involved in the regulation of gene expression and regulate a variety of proteins that essential for proper mitochondrial functioning. They are found to be dysregulated in PD, as evidenced by biological samples from PD patients and in vitro and in vivo research. In this article, we attempt to provide an overview of several miRNAs linked to mitochondrial dysfunction and their potential as diagnostic biomarkers and therapeutic targets in PD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473154PMC
http://dx.doi.org/10.3233/JAD-220449DOI Listing

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