Case-control study of the α-synuclein interacting protein gene and Parkinson's disease

被引:14
作者
Maraganore, DM
Farrer, MJ
Lesnick, TG
de Andrade, M
Bower, JH
Hernandez, D
Hardy, JA
Rocca, WA
机构
[1] Mayo Clin & Mayo Fdn, Dept Neurol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Hlth Sci Res, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Neurosci, Jacksonville, FL 32224 USA
[4] NIA, Neurogenet Lab, Bethesda, MD 20892 USA
关键词
Parkinson's disease; synphilin-1; alphasynuclein; parkin; susceptibility genes; association; interactions; SYNPHILIN-1; GENE; ASSOCIATION; SUSCEPTIBILITY; POLYMORPHISMS; MUTATIONS; HAPLOTYPES; SCREEN;
D O I
10.1002/mds.10547
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We conducted a case-control study of the alpha-synuclein-interacting protein gene (SNCAIP, also known as synphilin-1) and Parkinson's disease (PD). A total of 319 PD cases and 195 controls were genotyped for four SNCAIP variants, including a microsatellite repeat in intron 4 and three restriction fragment length polymorphisms (RFLP) proximal to the 5' terminal of exons 1, 4, and 6. None of the variants were found associated with PD, overall. Global score statistics were not significant for four, three, and two loci haplotypes. All four loci were in linkage disequilibrium for cases, controls, or both groups combined (P < 0.0001). Recursive partitioning showed no interactions between variants of the SNCAIP gene and variants of the alpha-synuclein gene (SNCA) or the parkin (PARK2) gene. (C) 2003 Movement Disorder Society.
引用
收藏
页码:1233 / 1239
页数:7
相关论文
共 41 条
  • [1] No pathogenic mutations in the synphilin-1 gene in Parkinson's disease
    Bandopadhyay, R
    de Silva, R
    Khan, N
    Graham, E
    Vaughan, J
    Engelender, S
    Ross, C
    Morris, H
    Morris, C
    Wood, NW
    Daniel, S
    Lees, A
    [J]. NEUROSCIENCE LETTERS, 2001, 307 (02) : 125 - 127
  • [2] Incidence and distribution of parkinsonism in Olmsted County, Minnesota, 1976-1990
    Bower, JH
    Maraganore, DM
    McDonnell, SK
    Rocca, WA
    [J]. NEUROLOGY, 1999, 52 (06) : 1214 - 1220
  • [3] Bower JH, 2000, MOVEMENT DISORD, V15, P819, DOI 10.1002/1531-8257(200009)15:5<819::AID-MDS1009>3.0.CO
  • [4] 2-P
  • [5] Breslow N E, 1980, IARC Sci Publ, P5
  • [6] Parkin ubiquitinates the α-synuclein-interacting protein, synphilin-1:: implications for Lewy-body formation in Parkinson disease
    Chung, KKK
    Zhang, Y
    Lim, KL
    Tanaka, Y
    Huang, H
    Gao, J
    Ross, CA
    Dawson, VL
    Dawson, TM
    [J]. NATURE MEDICINE, 2001, 7 (10) : 1144 - 1150
  • [7] Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions
    Engelender, S
    Kaminsky, Z
    Guo, X
    Sharp, AH
    Amaravi, RK
    Kleiderlein, JJ
    Margolis, RL
    Troncoso, JC
    Lanahan, AA
    Worley, PF
    Dawson, VL
    Dawson, TM
    Ross, CA
    [J]. NATURE GENETICS, 1999, 22 (01) : 110 - 114
  • [8] Organization of the human synphilin-1 gene, a candidate for Parkinson's disease
    Engelender, S
    Wanner, T
    Kleiderlein, JJ
    Wakabayashi, K
    Tsuji, S
    Takahashi, H
    Ashworth, R
    Margolis, RL
    Ross, CA
    [J]. MAMMALIAN GENOME, 2000, 11 (09) : 763 - 766
  • [9] Genetic analysis of synphilin-1 in familial Parkinson's disease
    Farrer, M
    Destée, A
    Levecque, C
    Singleton, A
    Engelender, S
    Becquet, E
    Mouroux, V
    Richard, F
    Defebvre, L
    Crook, R
    Hernandez, D
    Ross, CA
    Hardy, J
    Amouyel, P
    Chartier-Harlin, MC
    [J]. NEUROBIOLOGY OF DISEASE, 2001, 8 (02) : 317 - 323
  • [10] α-synuclein gene haplotypes are associated with Parkinson's disease
    Farrer, M
    Maraganore, DM
    Lockhart, P
    Singleton, A
    Lesnick, TG
    de Andrade, M
    West, A
    de Silva, R
    Hardy, J
    Hernandez, D
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (17) : 1847 - 1851