Key result
Genetic variants including PNPLA3 rs738409, TM6SF2 rs58542926, MBOAT7 rs641738, and GCKR are significantly associated with susceptibility to and progression of non-alcoholic fatty liver disease.
Why the study?
Non-alcoholic fatty liver disease has a rising global prevalence, and genetic predisposition plays a key role in its development and progression.
Specific genetic variants, notably PNPLA3 rs738409, play a significant role in NAFLD susceptibility and may serve as future noninvasive biomarkers.
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Background Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease showing a rising prevalence globally. Genetic predisposition plays a key role in the development and progression of the disease pathogenicity. Main body This paper summarizes genetic associations based on their influence on several metabolic aspects such as lipid metabolism, glucose metabolism, hepatic iron accumulation and cholesterol metabolism toward the NAFLD pathogenicity. Furthermore, we present variations in some epigenetic characters and the microRNA profile with regard to NAFLD. Conclusion As reported in many studies, the PNPLA3 rs738409 variant seems to be significantly associated with NAFLD susceptibility. Other gene variants like TM6SF2 rs58542926, MBOAT7 rs641738 and GCKR variants also appear to be more prevalent among NAFLD patients. We believe these genetic variants may provide insights into new trends in developing noninvasive biomarkers and identify their suitability in clinical practice in the future.
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Genetic summaries of NAFLD metabolic pathways support hypothesis generation; leaves open clinical translation pending validation studies.
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Samarasinghe et al. (2023) conducted a review in Non-alcoholic fatty liver disease (NAFLD). Genetic variants (PNPLA3, TM6SF2, MBOAT7, GCKR) was evaluated. Genetic variants including PNPLA3 rs738409, TM6SF2 rs58542926, MBOAT7 rs641738, and GCKR are significantly associated with susceptibility to and progression of non-alcoholic fatty liver disease.
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