Functional promoter region polymorphism of the proinflammatory chemokine IL-80 gene associates with Parkinson's disease in the Irish

被引:57
作者
Ross, OA
O'Neill, C
Rea, IM
Lynch, T
Gosal, D
Wallace, A
Curran, MD
Middleton, D
Gibson, JM
机构
[1] Queens Univ Belfast, Sch Biol & Biochem, Ctr Med Biol, Belfast BT9 7BL, Antrim, North Ireland
[2] Queens Univ Belfast, Dept Geriatr Med, Belfast BT9 7BL, Antrim, North Ireland
[3] Belfast City Hosp, No Ireland Reg Histocompatibil & Immunogenet Lab, Belfast BT9 7AD, Antrim, North Ireland
[4] Royal Victoria Hosp, Dept Neurol, Belfast BT12 6BA, Antrim, North Ireland
[5] Univ Ulster, Sch Biomed Sci, Coleraine BT52 1SA, Londonderry, North Ireland
[6] Mater Misericordiae Hosp, Dept Neurol, Dublin 7, Ireland
[7] Univ Coll Dublin, Dublin 2, Ireland
关键词
proinflammatory; polymorphism; interleukin-8; Parkinson's disease;
D O I
10.1016/j.humimm.2004.01.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Parkinson's disease (PD) is one of the most prevalent neurodegenerative disorders and is characterized by the progressive loss of dopamine neurons in the substantia nigra. There is increasing evidence to suggest the inflammatory response of the brain contributes to the pathogenesis of PD. This study investigated the frequency of polymorphism located in the critical promoter region of the proinflammatory cytokine genes: interleukin (lL)-2, IL-6, IL-8, and tumor necrosis factor alpha (TNF-alpha) within a cohort of patients with PD in comparison to a group of healthy elderly individuals. No association was observed for single nucleotide polymorphism in the promoter regions of the IL-2, IL-6, and TNF-alpha genes. The single nucleotide polymorphism in the chemokine IL-8 gene was observed to associate with PD and appeared to be independent of age at onset. This association further supports the theory that the proinflammatory response in the brains of patients with PD plays a role in the pathogenesis of the disease and warrants further investigation into the role of chemokines in the brain, and a more detailed analysis of the genetics involved in the immune response of the brain.
引用
收藏
页码:340 / 346
页数:7
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