The catechol-O-methyltransferase (COMT) inhibitor entacapone enhances the pharmacokinetic and clinical response to Sinemet CR in Parkinson's disease

被引:56
作者
Piccini, P
Brooks, DJ
Korpela, K
Pavese, N
Karlsson, M
Gordin, A
机构
[1] Hammersmith Hosp, Sch Med, Imperial Coll, Dept Neurol, London, England
[2] Orion Pharma, Res Ctr, Espoo, Finland
关键词
Parkinson's disease; entacapone; controlled release levodopa;
D O I
10.1136/jnnp.68.5.589
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives-Entacapone is a specific, potent, peripherally acting catechol-O-methyltransferase (COMT) inhibitor. It has been shown to improve the bioavailability of plasma levodopa and extend its clinical effect when used as an adjunct to standard levodopa preparations, but there is little experience of the effect of entacapone on controlled release levodopa preparations. Methods-A double blind, placebo controlled, single dose, randomised, cross over trial was performed in 14 patients with Parkinson's disease with motor fluctuations to investigate the clinical effect of a single dose of entacapone (200 mg) when administered with either standard levodopa-carbidopa (Sinemet(TM)) or controlled release levodopa-carbidopa preparations (Sinemet CRTM). Results-When entacapone was administered with standard Sinemet(TM) the duration of the clinical response to standard Sinemet(TM) was longer in comparison with the response after placebo (p=0.02). Moreover, in the same patients, entacapone significantly increased the duration of the clinical response to Sinemet CRTM (p=0.05) without prolonging the latency of response or enhancing dyskinesias. Conclusions-These data confirm the clinical efficacy of entacapone-standard Sinemet(TM) combination. They also indicate that adding entacapone to controlled release levodopa preparations might provide a useful treatment option in patients with Parkinson's disease with motor fluctuations. A double blind clinical. trial with a chronically administered entacapone-Sinemet CRTM combination is, however, required to verify this viewpoint.
引用
收藏
页码:589 / 594
页数:6
相关论文
共 38 条
[1]   EFFECT OF ENTACAPONE, A COMT INHIBITOR, ON THE PHARMACOKINETICS AND METABOLISM OF LEVODOPA AFTER ADMINISTRATION OF CONTROLLED-RELEASE LEVODOPA-CARBIDOPA IN VOLUNTEERS [J].
AHTILA, S ;
KAAKKOLA, S ;
GORDIN, A ;
KORPELA, K ;
HEINAVAARA, S ;
KARLSSON, M ;
WIKBERG, T ;
TUOMAINEN, P ;
MANNISTO, PT .
CLINICAL NEUROPHARMACOLOGY, 1995, 18 (01) :46-57
[2]  
BRANNAN T, 1981, NEUROLOGY, V41, P2596
[3]   STRIATAL D2 RECEPTOR STATUS IN PATIENTS WITH PARKINSONS-DISEASE, STRIATONIGRAL DEGENERATION, AND PROGRESSIVE SUPRANUCLEAR PALSY, MEASURED WITH C-11 RACLOPRIDE AND POSITRON EMISSION TOMOGRAPHY [J].
BROOKS, DJ ;
IBANEZ, V ;
SAWLE, GV ;
PLAYFORD, ED ;
QUINN, N ;
MATHIAS, CJ ;
LEES, AJ ;
MARSDEN, CD ;
BANNISTER, R ;
FRACKOWIAK, RSJ .
ANNALS OF NEUROLOGY, 1992, 31 (02) :184-192
[4]   CONTROLLED-RELEASE LEVODOPA CARBIDOPA .2. SINEMET CR4 TREATMENT OF RESPONSE FLUCTUATIONS IN PARKINSONS-DISEASE [J].
CEDARBAUM, JM ;
BRECK, L ;
KUTT, H ;
MCDOWELL, FH .
NEUROLOGY, 1987, 37 (10) :1607-1612
[5]  
ESTEGUY M, 1985, REV NEUROL, V141, P413
[6]   LEVODOPA PHARMACOKINETIC MECHANISMS AND MOTOR FLUCTUATIONS IN PARKINSONS-DISEASE [J].
FABBRINI, G ;
JUNCOS, J ;
MOURADIAN, MM ;
SERRATI, C ;
CHASE, TN .
ANNALS OF NEUROLOGY, 1987, 21 (04) :370-376
[7]  
Fahn S., RECENT DEV PARKINSON, V2, P153, DOI DOI 10.1002/ANA.410220556
[8]  
FRIEDHOFF AJ, 1977, RES COMMUN CHEM PATH, V16, P411
[9]  
Gibaldi M. P., 1982, PHARMACOKINETICS
[10]   A COMPARISON OF STANDARD MADOPAR AND CONTROLLED RELEASE MADOPAR IN PARKINSONS-DISEASE [J].
GRAHAM, JS ;
HENDERSON, JM ;
MORRIS, JGL ;
YIANNIKAS, C .
AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE, 1991, 21 (01) :11-15