2023
DOI: 10.2147/rmhp.s416592
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Genetic Variations of AKT1 are Associated with Risk Screening for Non-Alcoholic Fatty Liver Disease

Abstract: Protein kinase B (PKB/AKT) has shown a high profile in the research of metabolic diseases. This research sought to determine whether the AKT1 gene's single nucleotide polymorphisms (SNPs) and the risk of developing non-alcoholic fatty liver disease (NAFLD) were related. Patients and Methods: Recruited in this case-control study were 2693 subjects, including 815 with NAFLD and 1878 without NAFLD. Three SNPs of AKT1 (rs2494732, rs2494752 and rs1130233) were genotyped. To examine the correlation between SNPs and … Show more

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“…Genetic variations in AKT1 have been associated with NAFLD risk. [ 33 ] Forkhead box protein O1 (FoxO1) is the main target of insulin action, possibly leading to lipid and glucose metabolism disorders after being activated. [ 34 ] Adiponectin can improve NAFLD by inhibiting the FoxO1 expression via AKT1/FoxO1 signaling pathway.…”
Section: Discussionmentioning
confidence: 99%
“…Genetic variations in AKT1 have been associated with NAFLD risk. [ 33 ] Forkhead box protein O1 (FoxO1) is the main target of insulin action, possibly leading to lipid and glucose metabolism disorders after being activated. [ 34 ] Adiponectin can improve NAFLD by inhibiting the FoxO1 expression via AKT1/FoxO1 signaling pathway.…”
Section: Discussionmentioning
confidence: 99%