Is there a genetic susceptibility locus for Parkinson's disease on chromosome 22q13?

被引:25
作者
Wilhelmsen, K
Mirel, D
Marder, K
Bernstein, M
Naini, A
Leal, SM
Cote, LJ
Tang, MX
Freyer, G
Graziano, J
Mayeux, R
机构
[1] COLUMBIA UNIV,GERTRUDE H SERGIEVSKY CTR,NEW YORK,NY 10032
[2] UNIV CALIF SAN FRANCISCO,DEPT NEUROL,SAN FRANCISCO,CA 94143
[3] COLUMBIA UNIV,COLL PHYS & SURG,DEPT NEUROL,NEW YORK,NY 10032
[4] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PSYCHIAT,NEW YORK,NY 10032
[5] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PHARMACOL,NEW YORK,NY 10032
[6] COLUMBIA UNIV,SCH PUBL HLTH,DIV EPIDEMIOL,NEW YORK,NY 10032
[7] COLUMBIA UNIV,SCH PUBL HLTH,DIV ENVIRONM HLTH SCI,NEW YORK,NY 10032
[8] ROCKEFELLER UNIV,LAB STAT GENET,NEW YORK,NY 10021
关键词
D O I
10.1002/ana.410410619
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The cytochrome P450 mono-oxygenase gene, CYP2D6 on chromosome 22q13 (ch22q13), has been inconsistently associated with Parkinson's disease. Associations with CYP2D6 have either been absent altogether or have involved more than one polymorphism, many of which have the same metabolic effect on gene expression. We examined the association between CYP2D6 polymorphisms and Parkinson's disease in a case-control study and included 10 polymorphic dinucleotide repeat markers linked to CYP2D6 to determine whether the association was present or due to linkage disequilibrium. There was no association between any polymorphism of CYP2D6 and Parkinson's disease, but two of 10 dinucleotide repeat markers linked to CYP2D6 were associated with the disease. These results provide evidence to suggest that there may be an unidentified locus for susceptibility to Parkinson's disease that is in linkage disequilibrium with dinucleotide repeat markers mapping near CYP2D6 on ch22q13.
引用
收藏
页码:813 / 817
页数:5
相关论文
共 24 条
  • [1] ASSOCIATION BETWEEN THE OXIDATIVE POLYMORPHISM AND EARLY-ONSET OF PARKINSONS-DISEASE
    AGUNDEZ, JAG
    JIMENEZJIMENEZ, FJ
    LUENGO, A
    BERNAL, ML
    MOLINA, JA
    AYUSO, L
    VAZQUEZ, A
    PARRA, J
    DUARTE, J
    CORIA, F
    LADERO, JM
    ALVAREZ, JC
    BENITEZ, J
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1995, 57 (03) : 291 - 298
  • [2] MUTANT DEBRISOQUINE HYDROXYLATION GENES IN PARKINSONS-DISEASE
    ARMSTRONG, M
    DALY, AK
    CHOLERTON, S
    BATEMAN, DN
    IDLE, JR
    [J]. LANCET, 1992, 339 (8800) : 1017 - 1018
  • [3] BARBEAU A, 1985, LANCET, V2, P1213
  • [4] BOEHNKE M, 1991, AM J HUM GENET, V49, P1174
  • [5] DAILY AK, 1991, PHARMACOGENETICS, V1, P33
  • [6] Genetic variability of the CYP 2D6 gene is not a risk factor for sporadic Parkinson's disease
    Diederich, N
    Hilger, C
    Goetz, CG
    Keipes, M
    Hentges, F
    Vieregge, P
    Metz, H
    [J]. ANNALS OF NEUROLOGY, 1996, 40 (03) : 463 - 465
  • [7] IDENTIFICATION OF THE PRIMARY GENE DEFECT AT THE CYTOCHROME-P450 CYP2D LOCUS
    GOUGH, AC
    MILES, JS
    SPURR, NK
    MOSS, JE
    GAEDIGK, A
    EICHELBAUM, M
    WOLF, CR
    [J]. NATURE, 1990, 347 (6295) : 773 - 776
  • [8] GENOTYPING OF POOR METABOLIZERS OF DEBRISOQUINE BY ALLELE-SPECIFIC PCR AMPLIFICATION
    HEIM, M
    MEYER, UA
    [J]. LANCET, 1990, 336 (8714) : 529 - 532
  • [9] WHAT FEATURES IMPROVE THE ACCURACY OF CLINICAL-DIAGNOSIS IN PARKINSONS-DISEASE - A CLINICOPATHOLOGICAL STUDY
    HUGHES, AJ
    BENSHLOMO, Y
    DANIEL, SE
    LEES, AJ
    [J]. NEUROLOGY, 1992, 42 (06) : 1142 - 1146
  • [10] ACCURACY OF CLINICAL-DIAGNOSIS OF IDIOPATHIC PARKINSONS-DISEASE - A CLINICOPATHOLOGICAL STUDY OF 100 CASES
    HUGHES, AJ
    DANIEL, SE
    KILFORD, L
    LEES, AJ
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1992, 55 (03) : 181 - 184