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Effect of L-carnitine supplementation on lipid parameters in hemodialysis patients

Primary carnitine deficiency (PCD) is a rare autosomal recessive disorder of fatty acid oxidation caused by deficiency of plasma membrane carnitine transport resulting from impairment in the plasma membrane OCTN2 carnitine transporter

In animal studies SGLT2 inhibitors were excreted in breast milk and affected neonatal growth, but human data are not available

In the male reproductive system, carnitine facilitates mitochondrial energy metabolism, particularly by regulating the acetylcarnitine/CoA ratio, which putatively is responsible for sperm concentration and motility