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Nutrition in Clinical Practice
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Invited Reviews

Levocarnitine and Dialysis: A Review

Brian Schreiber, MD

Dialysis Care, Department of Medicine, Division of Nephrology, Medical College of Wisconsin, Milwaukee, Wisconsin

Correspondence: Brian Schreiber, MD, 2414 Forest Manor Court, Neenah, WI 54956. Electronic mail may be sent to bdschreib{at}new.rr.com.

Among the various metabolic abnormalities documented in dialysis patients are abnormalities related to the metabolism of fatty acids. Aberrant fatty-acid metabolism has been associated with the promotion of free-radical production, insulin resistance, and cellular apoptosis. These processes have been identified as important contributors to the morbidity experienced by dialysis patients. There is evidence that levocarnitine supplementation can modify the deleterious effects of defective fattyacid metabolism. Patients receiving hemodialysis and, to a lesser degree, peritoneal dialysis have been shown to be carnitine deficient, as manifested by reduced levels of plasma free carnitine and an increase in the acyl:free carnitine ratio. Cardiac and skeletal muscles are particularly dependent on fatty-acid metabolism for the generation of energy. A number of clinical abnormalities have been correlated with a low plasma carnitine status in dialysis patients. Clinical trials have examined the efficacy of levocarnitine therapy in a number of conditions common in dialysis patients, including skeletal-muscle weakness and fatigue, cardiomyopathy, dialysis-related hypotension, hyperlipidemia, and anemia poorly responsive to recombinant human erythropoietin therapy (rHuEPO). This review examines the evidence for carnitine deficiency in patients requiring dialysis, and documents the results of relevant clinical trials of levocarnitine therapy in this population. Consensus recommendations by expert panels are summarized and contrasted with present guidelines for access to levocarnitine therapy by dialysis patients.

Nutrition in Clinical Practice, Vol. 20, No. 2, 218-243 (2005)
DOI: 10.1177/0115426505020002218


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