PMID- 17963454 OWN - NLM STAT- MEDLINE DCOM- 20080401 LR - 20161018 IS - 1434-6621 (Print) IS - 1434-6621 (Linking) VI - 45 IP - 12 DP - 2007 TI - Management of L-Dopa related hyperhomocysteinemia: catechol-O-methyltransferase (COMT) inhibitors or B vitamins? Results from a review. PG - 1607-13 AB - In recent years, L-Dopa treatment has been indicated as an acquired cause of hyperhomocysteinemia (HHcy). The mechanism underlying L-Dopa-related HHcy is the O-methylation of the drug catalyzed by the enzyme catechol-O-methyltransferase (COMT). Folate and cobalamin status also influences the effects of L-Dopa on plasma homocysteine (Hcy) levels. Although clinical correlations of HHcy in Parkinson's disease still remain uncertain, management of elevated plasma Hcy levels has been advocated, due to multiple cytotoxic effects of Hcy on neurons. This review summarizes data available in the literature concerning the two main therapeutic approaches to L-Dopa-related HHcy (use of COMT inhibitors or B vitamins diet supplementation). FAU - Zoccolella, Stefano AU - Zoccolella S AD - Department of Neurological Sciences, University of Bari, Bari, Italy. FAU - Iliceto, Giovanni AU - Iliceto G FAU - deMari, Michele AU - deMari M FAU - Livrea, Paolo AU - Livrea P FAU - Lamberti, Paolo AU - Lamberti P LA - eng PT - Journal Article PT - Review PL - Germany TA - Clin Chem Lab Med JT - Clinical chemistry and laboratory medicine JID - 9806306 RN - 0 (Catechol O-Methyltransferase Inhibitors) RN - 0 (Enzyme Inhibitors) RN - 12001-76-2 (Vitamin B Complex) RN - 46627O600J (Levodopa) SB - IM MH - *Catechol O-Methyltransferase Inhibitors MH - Enzyme Inhibitors/*pharmacology MH - Humans MH - Hyperhomocysteinemia/*chemically induced MH - Levodopa/*adverse effects MH - Vitamin B Complex/*pharmacology RF - 49 EDAT- 2007/10/30 09:00 MHDA- 2008/04/02 09:00 CRDT- 2007/10/30 09:00 PHST- 2007/10/30 09:00 [pubmed] PHST- 2008/04/02 09:00 [medline] PHST- 2007/10/30 09:00 [entrez] AID - 10.1515/CCLM.2007.337 [doi] PST - ppublish SO - Clin Chem Lab Med. 2007;45(12):1607-13. doi: 10.1515/CCLM.2007.337.