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doi: 10.3164/jcbn.19-87 110

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Evidence supports an association between the diseases, but the exact underlying mechanisms behind the connection are still under investigation

Historical considerations and treatment]

Inborn errors Congenital defects involve enzyme deficiencies in the carnitine transport or metabolic pathways, such as CPT II deficiency, which affects the function of the carnitine transporter CPT II and leads to impaired fatty acid -oxidation, and CACT deficiency, which affects the function of the carnitine transporter CACT and results in carnitine shuttle dysfunction

It has the ability to scavenge free radicals, which helps to delay the aging process