Modest increase in plasma homocysteine follows levodopa initiation in Parkinson's disease
Levodopa, typically ingested chronically at high daily doses, is predictably methylated by means of a series of reactions using B vitamins, which convert methionine to homocysteine. Elevated total plasma homocysteine (tHcy), a risk factor for dementia, has been found in PD patients using levodopa. W...
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description | Levodopa, typically ingested chronically at high daily doses, is predictably methylated by means of a series of reactions using B vitamins, which convert methionine to homocysteine. Elevated total plasma homocysteine (tHcy), a risk factor for dementia, has been found in PD patients using levodopa. We prospectively measured the effects on plasma tHcy and B vitamins of levodopa initiation, and measured the effects of dose changes and of treatment with dopamine agonists and entacapone. We collected paired plasma samples, at baseline and again after several months treatment, from patients initiating levodopa (n = 30), from patients whose levodopa dose was doubled (n = 15), halved or stopped (n = 14), from patients starting or stopping entacapone (n = 15) and from patients initiating or doubling dopamine agonist monotherapy (n = 16). Vitamin B12, folate, and tHcy concentrations were measured. Baseline tHcy concentration of 8.7 (2.8) μmol/L increased to 10.1 (3.1) μmol/L (P = 0.004) an average of 94 (range 36 to 200) days after initiation of 604 (240 to 1050) mg/day of L‐dopa. Average concentration of vitamin B12 fell from 380 to 291 pmol/ L (P = 0.01). Patients who doubled their daily levodopa dose experienced tHcy elevations from 9.5 to 11.1 μmol/L (P = 0.05). Levodopa reduction, agonist treatment, and entacapone treatment did not have significant effects. Levodopa elevates tHcy and lowers vitamin B12 concentration to modest degrees. The clinical implications, if any, have not yet been determined. © 2004 Movement Disorder Society |
doi_str_mv | 10.1002/mds.20253 |
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Elevated total plasma homocysteine (tHcy), a risk factor for dementia, has been found in PD patients using levodopa. We prospectively measured the effects on plasma tHcy and B vitamins of levodopa initiation, and measured the effects of dose changes and of treatment with dopamine agonists and entacapone. We collected paired plasma samples, at baseline and again after several months treatment, from patients initiating levodopa (n = 30), from patients whose levodopa dose was doubled (n = 15), halved or stopped (n = 14), from patients starting or stopping entacapone (n = 15) and from patients initiating or doubling dopamine agonist monotherapy (n = 16). Vitamin B12, folate, and tHcy concentrations were measured. Baseline tHcy concentration of 8.7 (2.8) μmol/L increased to 10.1 (3.1) μmol/L (P = 0.004) an average of 94 (range 36 to 200) days after initiation of 604 (240 to 1050) mg/day of L‐dopa. Average concentration of vitamin B12 fell from 380 to 291 pmol/ L (P = 0.01). Patients who doubled their daily levodopa dose experienced tHcy elevations from 9.5 to 11.1 μmol/L (P = 0.05). Levodopa reduction, agonist treatment, and entacapone treatment did not have significant effects. Levodopa elevates tHcy and lowers vitamin B12 concentration to modest degrees. The clinical implications, if any, have not yet been determined. © 2004 Movement Disorder Society</description><identifier>ISSN: 0885-3185</identifier><identifier>EISSN: 1531-8257</identifier><identifier>DOI: 10.1002/mds.20253</identifier><identifier>PMID: 15390053</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Antiparkinson Agents - adverse effects ; Antiparkinson Agents - therapeutic use ; Biological and medical sciences ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; dopamine agonists ; Drug toxicity and drugs side effects treatment ; Folic Acid - metabolism ; homocysteine ; Humans ; Hyperhomocysteinemia - chemically induced ; Hyperhomocysteinemia - epidemiology ; levodopa ; Levodopa - adverse effects ; Levodopa - therapeutic use ; Medical sciences ; Middle Aged ; Neurology ; Parkinson Disease - blood ; Parkinson Disease - drug therapy ; Parkinson's disease ; Pharmacology. 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Disord</addtitle><description>Levodopa, typically ingested chronically at high daily doses, is predictably methylated by means of a series of reactions using B vitamins, which convert methionine to homocysteine. Elevated total plasma homocysteine (tHcy), a risk factor for dementia, has been found in PD patients using levodopa. We prospectively measured the effects on plasma tHcy and B vitamins of levodopa initiation, and measured the effects of dose changes and of treatment with dopamine agonists and entacapone. We collected paired plasma samples, at baseline and again after several months treatment, from patients initiating levodopa (n = 30), from patients whose levodopa dose was doubled (n = 15), halved or stopped (n = 14), from patients starting or stopping entacapone (n = 15) and from patients initiating or doubling dopamine agonist monotherapy (n = 16). Vitamin B12, folate, and tHcy concentrations were measured. Baseline tHcy concentration of 8.7 (2.8) μmol/L increased to 10.1 (3.1) μmol/L (P = 0.004) an average of 94 (range 36 to 200) days after initiation of 604 (240 to 1050) mg/day of L‐dopa. Average concentration of vitamin B12 fell from 380 to 291 pmol/ L (P = 0.01). Patients who doubled their daily levodopa dose experienced tHcy elevations from 9.5 to 11.1 μmol/L (P = 0.05). Levodopa reduction, agonist treatment, and entacapone treatment did not have significant effects. Levodopa elevates tHcy and lowers vitamin B12 concentration to modest degrees. The clinical implications, if any, have not yet been determined. © 2004 Movement Disorder Society</description><subject>Aged</subject><subject>Antiparkinson Agents - adverse effects</subject><subject>Antiparkinson Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>dopamine agonists</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Folic Acid - metabolism</subject><subject>homocysteine</subject><subject>Humans</subject><subject>Hyperhomocysteinemia - chemically induced</subject><subject>Hyperhomocysteinemia - epidemiology</subject><subject>levodopa</subject><subject>Levodopa - adverse effects</subject><subject>Levodopa - therapeutic use</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Parkinson Disease - blood</subject><subject>Parkinson Disease - drug therapy</subject><subject>Parkinson's disease</subject><subject>Pharmacology. Drug treatments</subject><subject>Prospective Studies</subject><subject>Toxicity: nervous system and muscle</subject><subject>Vitamin B 12 - metabolism</subject><issn>0885-3185</issn><issn>1531-8257</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kE1v1DAQhi0EokvhwB9AuQDikNZjx3FyRFsoqFuoVD7KyZrYjjA48TazS9l_j5dd2hOnmcPzvqN5GHsK_Ag4F8eDoyPBhZL32AyUhLIRSt9nM940qpTQqAP2iOgH5wAK6ofsIEMt50rO2Lfz5DytijDaySP5vBTLiDRg8T0NyW5o5cPoiz7FmG6oiP5XcmmJmQurgKuQxm3kAqefYaQ0vqTCBdo2PWYPeozkn-znIfv89s2n-bty8fH0_fz1orSVELJ0vlJOayuEbxuonOiU5B1o3yIKy61uqrrv2kpgbXtA0KqrOo41uI63PbbykL3Y9S6ndL3Ov5ghkPUx4ujTmowAqKTUIoOvdqCdEtHke7OcwoDTxgA3W48mezR_PWb22b503Q3e3ZF7cRl4vgeQLMZ-wtEGuuNqqSvRbrnjHXcTot_8_6I5P7n8d7rcJUJW__s2kQWbWkutzNcPp2a--HJ5dXEG5kr-Ad4Rmbk</recordid><startdate>200412</startdate><enddate>200412</enddate><creator>O'Suilleabhain, Padraig E.</creator><creator>Bottiglieri, Teodoro</creator><creator>Dewey Jr, Richard B.</creator><creator>Sharma, Shailja</creator><creator>Diaz-Arrastia, Ramon</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope></search><sort><creationdate>200412</creationdate><title>Modest increase in plasma homocysteine follows levodopa initiation in Parkinson's disease</title><author>O'Suilleabhain, Padraig E. ; Bottiglieri, Teodoro ; Dewey Jr, Richard B. ; Sharma, Shailja ; Diaz-Arrastia, Ramon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4223-de45d77c22e9814d2b530b17e9aa2c0c7846fb942a6cf1a175b4b0a61db09fa93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aged</topic><topic>Antiparkinson Agents - adverse effects</topic><topic>Antiparkinson Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</topic><topic>dopamine agonists</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Folic Acid - metabolism</topic><topic>homocysteine</topic><topic>Humans</topic><topic>Hyperhomocysteinemia - chemically induced</topic><topic>Hyperhomocysteinemia - epidemiology</topic><topic>levodopa</topic><topic>Levodopa - adverse effects</topic><topic>Levodopa - therapeutic use</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Parkinson Disease - blood</topic><topic>Parkinson Disease - drug therapy</topic><topic>Parkinson's disease</topic><topic>Pharmacology. Drug treatments</topic><topic>Prospective Studies</topic><topic>Toxicity: nervous system and muscle</topic><topic>Vitamin B 12 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>O'Suilleabhain, Padraig E.</creatorcontrib><creatorcontrib>Bottiglieri, Teodoro</creatorcontrib><creatorcontrib>Dewey Jr, Richard B.</creatorcontrib><creatorcontrib>Sharma, Shailja</creatorcontrib><creatorcontrib>Diaz-Arrastia, Ramon</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><jtitle>Movement disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>O'Suilleabhain, Padraig E.</au><au>Bottiglieri, Teodoro</au><au>Dewey Jr, Richard B.</au><au>Sharma, Shailja</au><au>Diaz-Arrastia, Ramon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modest increase in plasma homocysteine follows levodopa initiation in Parkinson's disease</atitle><jtitle>Movement disorders</jtitle><addtitle>Mov. Disord</addtitle><date>2004-12</date><risdate>2004</risdate><volume>19</volume><issue>12</issue><spage>1403</spage><epage>1408</epage><pages>1403-1408</pages><issn>0885-3185</issn><eissn>1531-8257</eissn><abstract>Levodopa, typically ingested chronically at high daily doses, is predictably methylated by means of a series of reactions using B vitamins, which convert methionine to homocysteine. Elevated total plasma homocysteine (tHcy), a risk factor for dementia, has been found in PD patients using levodopa. We prospectively measured the effects on plasma tHcy and B vitamins of levodopa initiation, and measured the effects of dose changes and of treatment with dopamine agonists and entacapone. We collected paired plasma samples, at baseline and again after several months treatment, from patients initiating levodopa (n = 30), from patients whose levodopa dose was doubled (n = 15), halved or stopped (n = 14), from patients starting or stopping entacapone (n = 15) and from patients initiating or doubling dopamine agonist monotherapy (n = 16). Vitamin B12, folate, and tHcy concentrations were measured. Baseline tHcy concentration of 8.7 (2.8) μmol/L increased to 10.1 (3.1) μmol/L (P = 0.004) an average of 94 (range 36 to 200) days after initiation of 604 (240 to 1050) mg/day of L‐dopa. Average concentration of vitamin B12 fell from 380 to 291 pmol/ L (P = 0.01). Patients who doubled their daily levodopa dose experienced tHcy elevations from 9.5 to 11.1 μmol/L (P = 0.05). Levodopa reduction, agonist treatment, and entacapone treatment did not have significant effects. Levodopa elevates tHcy and lowers vitamin B12 concentration to modest degrees. The clinical implications, if any, have not yet been determined. © 2004 Movement Disorder Society</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15390053</pmid><doi>10.1002/mds.20253</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Antiparkinson Agents - adverse effects Antiparkinson Agents - therapeutic use Biological and medical sciences Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases dopamine agonists Drug toxicity and drugs side effects treatment Folic Acid - metabolism homocysteine Humans Hyperhomocysteinemia - chemically induced Hyperhomocysteinemia - epidemiology levodopa Levodopa - adverse effects Levodopa - therapeutic use Medical sciences Middle Aged Neurology Parkinson Disease - blood Parkinson Disease - drug therapy Parkinson's disease Pharmacology. Drug treatments Prospective Studies Toxicity: nervous system and muscle Vitamin B 12 - metabolism |
title | Modest increase in plasma homocysteine follows levodopa initiation in Parkinson's disease |
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