What is carnitine deficiency?

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    Last Updated: May 16, 2025

    Carnitine deficiency is rare and can occur in children with genetic metabolic disorders, with use of certain medications, or in people who are undergoing dialysis for chronic kidney disease. Although people who are on strict plant-based diets typically synthesize enough carnitine from other amino acids, supplementation may be used to treat symptoms in the case of deficiency, though more research is needed to confirm its effectiveness.

    Although the main dietary source of carnitine is meat,[1][2] people who follow a strict plant-based diet typically do not have a higher risk of carnitine deficiency because sufficient amounts of carnitine can be synthesized in the body from other amino acids (e.g., lysine and methionine).[3][4]

    In rare cases, carnitine deficiency can occur in children with inborn errors of metabolism (i.e., genetic defects affecting metabolic function) in carnitine biosynthetic or carnitine transport pathways.[5][6] Carnitine deficiency can also be caused by some drugs, including pivalic-acid-containing antibiotics and valproic acid, and it can occur in response to dialysis in people with chronic kidney disease.[5][6] In such cases, supplementation with carnitine is sometimes used to help treat the symptoms, but high-quality randomized controlled trials are needed to confirm its efficacy.[7][5][6]