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Genetic and epigenetic determinants of non-alcoholic fatty liver disease (NAFLD) in lean individuals: a systematic review. | LitMetric

AI Article Synopsis

  • - The study focuses on non-alcoholic fatty liver disease (NAFLD) in lean individuals, aiming to review genetic and epigenetic factors influencing its occurrence, as this area is not well understood.
  • - A total of 18 peer-reviewed studies were analyzed, revealing moderate quality with variations in risk of bias; several genetic variants linked to lipid metabolism and inflammation were identified, alongside some epigenetic changes like histone depletion.
  • - The findings emphasize the need for more research to clarify the genetic and epigenetic mechanisms of NAFLD in lean individuals and suggest that both genetic variants and epigenetic factors may play a significant role.

Article Abstract

Background: Non-alcoholic fatty liver disease (NAFLD) is common in obese individuals, but its occurrence in lean individuals and the underlying mechanisms are not well understood. This study aimed to systematically review the literature on the genetic and epigenetic factors influencing NAFLD in lean individuals.

Methods: A comprehensive search was conducted on April 2, 2023, in seven databases using specific criteria. Only peer-reviewed studies in English, focusing on genetic or epigenetic effects on NAFLD in lean individuals, were included for qualitative synthesis. The Newcastle Ottawa Scale (NOS) was used for quality assessment. This study is registered with PROSPERO (CRD42023413809).

Results: Following PRISMA guidelines, 18 studies were included in this review. The studies were conducted globally, with varying sample sizes and study designs. The NOS quality assessment revealed a moderate overall quality with variations in risk of bias and limitations in comparability and ascertainments of exposure among contributing studies. Genetic determinants related to lipid metabolism, inflammation, and oxidative stress pathways were identified, including and gene variants associated with increased NAFLD risk in lean individuals. Epigenetic modifications, particularly depletion of histone variants, were also implicated. However, some studies found no significant associations between genetic or clinical characteristics and lean NAFLD. Less frequent genetic risk factors, such as and gene variants, were reported.

Conclusions: This systematic review underscores the importance of investigating genetic and epigenetic factors in lean NAFLD. The findings highlight the role of and gene variants and suggest potential epigenetic contributions. Further research is needed to fully understand the genetic and epigenetic mechanisms underlying NAFLD in lean individuals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10838615PMC
http://dx.doi.org/10.21037/tgh-23-31DOI Listing

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