脂肪生成
胰岛素抵抗
非诺贝特
脂肪肝
医学
血脂异常
脂肪变性
内科学
内分泌学
脂质代谢
脂肪性肝炎
非酒精性脂肪肝
甘油三酯
胆固醇
胰岛素
疾病
作者
Shima Dowla Anwar,Christy Foster,Ambika P. Ashraf
标识
DOI:10.1016/j.ecl.2023.01.003
摘要
Dyslipidemia has been linked metabolic-associated fatty liver disease (MAFLD). Several genes and transcription factors involved in lipid metabolism can increase susceptibility to MAFLD. Multiple parallel ‘hits’ have been proposed for developing hepatic steatosis, NASH , and MAFLD, including insulin resistance and subsequent free fatty acid excess, de novo lipogenesis , and excessive hepatic triglyceride and cholesterol deposition in the liver. This lead to defective beta-oxidation in the mitochondria and VLDL export and increased inflammation. Given the significant cardiovascular risk, dyslipidemia associated with MAFLD should be managed by lifestyle changes and lipid-lowering agents such as statins, fenofibrate , and omega-3 fatty acids, with judicious use of insulin-sensitizing agents, and adequate control of dysglycemia .
科研通智能强力驱动
Strongly Powered by AbleSci AI