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NOS2A and the modulating effect of cigarette smoking in Parkinson's disease
被引:29
作者:

Hancock, Dana B.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Martin, Eden R.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Fujiwara, Kenichiro
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Stacy, Mark A.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Scott, Burton L.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Stajich, Jeffrey M.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Jewett, Rita
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Li, Yi-Ju
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Hauser, Michael A.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Vance, Jeffery M.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA

Scott, William K.
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机构: Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
机构:
[1] Duke Univ, Med Ctr, Ctr Human Genet, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
关键词:
D O I:
10.1002/ana.20915
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Objective: Inducible nitric oxide synthase, a protein product of NOS2A, generates nitric oxide as a defense mechanism, but excessive levels threaten cellular survival. NOS2A is a candidate gene for Parkinson's disease (PD) that potentially interacts with cigarette smoking. We examined NOS2A for association with PD risk and age at onset (AAO) and for interaction with smoking. Methods: We genotyped 13 NOS2A single nucleotide polymorphisms (SNPs) in 466 singleton families and in a validation set of 286 multiplex families. We tested allelic and haplotypic association using the association in the presence of linkage test, genotypic associations using the genotype pedigree disequilibrium test, AAO effects using the quantitative transmission disequilibrium test, and interactions using generalized estimating equations. Results: Among the pooled earliest onset families, rs2255929 and rs1060826 generated significant allelic (p = 0.000059 and 0.0062, respectively) and genotypic (p = 0.0039 and 0.0014, respectively) associations with risk and AAO (p = 0.00070 and 0.0073, respectively); the two-SNP haplotype generated even stronger association with PD (p = 0.000013). Significant interactions with smoking (p = 0.0015 for rs 2255929 and p < 0.0001 for rs 1060826) were detected in a subset of the families; smoking was inversely associated with PD among risk allele noncarriers, but significance diminished among carriers. Interpretation: Our findings support NOS2A as a genetic risk factor in PD, potentially by influencing AAO and by modifying the inverse association between PD and smoking.
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页码:366 / 373
页数:8
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