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(Etiology) Carnitine Deficiency Syndrome is a metabolic muscle disease that is characterized by an interference with fat processing needed for the production of energy (fat metabolism that turns fat into energy) Carnitine Deficiency Syndrome can be either primary or secondary: This condition is caused by a genetic defect in the protein (carnitine transporter protein) that is responsible for transporting carnitine into the cell

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Mechanistically, the peptide perturbs the FOXO4 interaction with p53, which selectively causes p53 nuclear exclusion and cell-intrinsic apoptosis (Baar et al., 2017)

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I also think that people who haven't battled with their weight, they can also sympathize or empathize as well, but I think maybe a little more difficult