2022
DOI: 10.1016/j.bcp.2022.115242
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Mineral metabolism and ferroptosis in non-alcoholic fatty liver diseases

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Cited by 36 publications
(20 citation statements)
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“… 43 A plethora of research work has explored the role and mechanism of iron metabolism, iron deposition, and ferroptosis in MAFLD, and researchers have reviewed and discussed this in considerable detail. 44–46 Biopsies confirm poorer long-term outcomes in patients with NAFLD and iron overload, 47 which may be due to elevated insulin resistance, excess hepatic lipid peroxidation, and iron overload contributing to the progression of liver fibrosis. GPX4-reduced ferroptosis is a crucial trigger for MAFLD progression to NASH.…”
Section: Ferroptosis In Metabolism-related Fatty Liver Diseasementioning
confidence: 99%
“… 43 A plethora of research work has explored the role and mechanism of iron metabolism, iron deposition, and ferroptosis in MAFLD, and researchers have reviewed and discussed this in considerable detail. 44–46 Biopsies confirm poorer long-term outcomes in patients with NAFLD and iron overload, 47 which may be due to elevated insulin resistance, excess hepatic lipid peroxidation, and iron overload contributing to the progression of liver fibrosis. GPX4-reduced ferroptosis is a crucial trigger for MAFLD progression to NASH.…”
Section: Ferroptosis In Metabolism-related Fatty Liver Diseasementioning
confidence: 99%
“…Because of the lack of efficient diagnostic methods and therapeutic targets, early detection and treatment of NAFLD still face many challenges. The underlying mechanism for the pathogenesis and progression of NAFLD is complex, and disturbance in trace element and mineral metabolism and interactions have been identified as one of the key risk factors of this disease ( 169 , 170 ). As NAFLD is closely associated with the components of MetS, obesity, and T2DM, a change in nomenclature from NAFLD to metabolic-associated fatty liver disease (MAFLD) has been recently proposed, which may better reflect the underlying pathophysiology of this disease ( 171 ).…”
Section: Recent Progress In Ionomics Of Metabolic Diseasesmentioning
confidence: 99%
“…Copper is an indispensable trace element that serves as a structural and enzymatic cofactor for various antioxidant proteins, including cytochrome c oxidase (COX), superoxide dismutase (SOD), and ceruloplasmin ( 7 ). Excessive or deficient copper can lead to mitochondrial dysfunction or dyslipidemia ( 8 ). A typical example is Wilson's disease, an overloaded hepatic copper accumulation and insufficient ceruloplasmin with liver steatosis, inflammation, and cuprotosis ( 9 ).…”
Section: Introductionmentioning
confidence: 99%
“…Whereas, the relationship between serum/hepatic copper levels and NAFLD is still unclear. What's more, it is reported that lower hepatic copper is associated with NAFLD, but excessive copper also impairs hepatocytes ( 8 , 13 ). Lan, et al find that blood copper concentration is lower in NAFLD patients ( 14 ).…”
Section: Introductionmentioning
confidence: 99%