The sparteine/debrisoquine (CYP2D6) oxidation polymorphism and the risk ofParkinson's disease: a meta-analysis

Citation
Pm. Christensen et al., The sparteine/debrisoquine (CYP2D6) oxidation polymorphism and the risk ofParkinson's disease: a meta-analysis, PHARMACOGEN, 8(6), 1998, pp. 473-479
Citations number
35
Categorie Soggetti
Pharmacology & Toxicology
Journal title
PHARMACOGENETICS
ISSN journal
0960314X → ACNP
Volume
8
Issue
6
Year of publication
1998
Pages
473 - 479
Database
ISI
SICI code
0960-314X(199812)8:6<473:TS(OPA>2.0.ZU;2-5
Abstract
The association between the sparteine/debrisoquine (CYP2D6) oxidation polym orphism and the risk of Parkinson's disease was examined in a meta-analysis of case-control studies. The odds ratio was calculated for the risk of Par kinson's disease among poor metabolisers compared with extensive metabolise rs. Twenty-one studies were identified of which six were excluded because t hey were not reported as full papers (n = 3), used incomplete genotype anal ysis (n = 2) or used Parkinson patients as both control individuals and cas es (n = 1). The overall odds ratio was 1.48 (95% confidence interval 1.10-1 .99). The odds ratio was 1.05 (95% confidence interval 0.63-1.77) in studie s discriminating extensive and poor metabolisers by phenotyping (n = 8) and 1.67 (95% confidence interval 1.11-2.50) in studies using genotyping (n = 7). This difference was caused by a single large study using genotyping. We conclude that there is no convincing evidence of an association between th e debrisoquine/sparteine polymorphism and Parkinson's disease. However, it could prove worthwhile to perform another large study using genotyping. Pha rmacogenetics 8:473-479. (C) 1998 Lippincott Williams & Wilkins.