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MMP-9 与帕金森病和肌萎缩性侧索硬化症的关联研究。

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

机构信息

Department of Neurology, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China.

出版信息

PLoS One. 2013 Sep 9;8(9):e73777. doi: 10.1371/journal.pone.0073777. eCollection 2013.

Abstract

Parkinson's disease (PD) and amyotrophic lateral sclerosis (ALS) share several clinical and neuropathologic features, and studies suggest that several gene mutations and polymorphisms are involved in both conditions. Matrix metalloproteinase-9 (MMP-9) is implicated in the pathogenesis of PD and ALS, and the C(-1562)T polymorphism in the MMP-9 gene leads to higher promoter activity. We therefore investigated whether this polymorphism predisposes to both PD and sporadic ALS (sALS). Samples from 351 subjects with PD and 351 healthy controls from two major cities in China were compared, while samples from 226 subjects with sALS were compared to the same number of controls from three centers in China. A possible association between the C(-1562)T polymorphism in the MMP-9 gene and PD or sALS was assessed by restriction fragment length polymorphism (RFLP) analysis. Our results show a significant association between the C(-1562)T polymorphism in the MMP-9 gene and risk of PD (odds ratio = 2.268, 95% CI 1.506-3.416, p<0.001) as well as risk of sALS (odds ratio = 2.163, 95% CI 1.233-3.796, p = 0.006), supporting a role for MMP-9 polymorphism in the risk for PD and sALS.

摘要

帕金森病(PD)和肌萎缩侧索硬化症(ALS)具有一些相似的临床和神经病理学特征,研究表明,几种基因突变和多态性与这两种疾病都有关。基质金属蛋白酶-9(MMP-9)参与了 PD 和 ALS 的发病机制,MMP-9 基因中的 C(-1562)T 多态性导致启动子活性增加。因此,我们研究了这种多态性是否会导致 PD 和散发性 ALS(sALS)。我们比较了来自中国两个主要城市的 351 名 PD 患者和 351 名健康对照者的样本,同时还比较了来自中国三个中心的 226 名 sALS 患者与相同数量的对照者的样本。通过限制性片段长度多态性(RFLP)分析评估 MMP-9 基因 C(-1562)T 多态性与 PD 或 sALS 之间的可能关联。我们的结果显示,MMP-9 基因中的 C(-1562)T 多态性与 PD (比值比=2.268,95%可信区间 1.506-3.416,p<0.001)和 sALS (比值比=2.163,95%可信区间 1.233-3.796,p=0.006)的风险显著相关,这支持 MMP-9 多态性在 PD 和 sALS 风险中的作用。

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本文引用的文献

1
Investigation of c9orf72 in 4 neurodegenerative disorders.
Arch Neurol. 2012 Dec;69(12):1583-90. doi: 10.1001/archneurol.2012.2016.
2
Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases.
Neurology. 2012 Aug 28;79(9):878-82. doi: 10.1212/WNL.0b013e3182661d14. Epub 2012 Jul 25.
4
Large C9orf72 repeat expansions are not a common cause of Parkinson's disease.
Neurobiol Aging. 2012 Oct;33(10):2527.e1-2. doi: 10.1016/j.neurobiolaging.2012.05.007. Epub 2012 Jun 20.
5
Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis.
Ann Neurol. 2011 Dec;70(6):964-73. doi: 10.1002/ana.22611.
6
Dysregulation of iron metabolism in Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis.
Adv Pharmacol Sci. 2011;2011:378278. doi: 10.1155/2011/378278. Epub 2011 Oct 12.
7
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.
Neurogenetics. 2011 Aug;12(3):203-9. doi: 10.1007/s10048-011-0288-3. Epub 2011 Jun 11.
8
Ataxin-2 repeat-length variation and neurodegeneration.
Hum Mol Genet. 2011 Aug 15;20(16):3207-12. doi: 10.1093/hmg/ddr227. Epub 2011 May 24.
9
EMMPRIN levels in serum of patients with amyotrophic lateral sclerosis.
Acta Neurol Scand. 2011 Dec;124(6):424-8. doi: 10.1111/j.1600-0404.2011.01519.x. Epub 2011 May 7.
10
Intracellular substrate cleavage: a novel dimension in the biochemistry, biology and pathology of matrix metalloproteinases.
Crit Rev Biochem Mol Biol. 2010 Oct;45(5):351-423. doi: 10.3109/10409238.2010.501783.

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