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Abstract The global epidemic of non-alcoholic fatty liver disease (NAFLD) and steatohepatitis (NASH) and the high prevalence among individuals with type 2 diabetes has attracted the attention of clinicians specialising in liver disorders

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Based on these findings, clinical trials, particularly those involving Exenatide and Lixisenatide, have explored their potential to modify the course of PD, however, recent findings have been less promising than anticipated

54,55 By doing so, the resulting product has a higher similarity or homology to the amino acid sequence of human GLP-1