MUTANT DEBRISOQUINE HYDROXYLATION GENES IN PARKINSONS-DISEASE

被引:245
作者
ARMSTRONG, M
DALY, AK
CHOLERTON, S
BATEMAN, DN
IDLE, JR
机构
[1] MED SCH NEWCASTLE UPON TYNE,DEPT PHARMACOL SCI,PHARMACOGENET RES UNIT,FRAMLINGTON PL,NEWCASTLE TYNE NE2 4HH,ENGLAND
[2] MED SCH NEWCASTLE UPON TYNE,WOLFSON UNIT CLIN PHARMACOL,NEWCASTLE TYNE NE2 4HH,ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1016/0140-6736(92)90537-D
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The frequency of fifteen genotypes of CYP2D6 (debrisoquine 4-hydroxylase) in 53 patients with Parkinson's disease was determined by the polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) analyses and compared with the findings in 72 healthy controls. The commonest mutant allele, CYP2D6B, was twice as frequent among patients as in controls, with an approximate relative risk ratio of 2.70 (95% confidence interval 1.14-6.41; p = 0.0063) for subjects homozygous or heterozygous for this allele.
引用
收藏
页码:1017 / 1018
页数:2
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