Pola Roberto, Flex Andrea, Gaetani Eleonora, Proia Anna S, Papaleo Pierangelo, Di Giorgio Angela, Straface Giuseppe, Pecorini Giovanni, Serricchio Michele, Pola Paolo
Laboratory of Vascular Biology and Genetics, Department of Medicine, A. Gemelli University Hospital, Università Cattolica del Sacro Cuore School of Medicine, Rome, Italy.
Exp Gerontol. 2004 Aug;39(8):1249-52. doi: 10.1016/j.exger.2004.05.001.
Monocyte chemoattractant protein-1 (MCP-1) is a key molecule for monocyte chemotaxis and tissue extravasation and for the modulation of leukocyte function during inflammation. Upregulation of MCP-1 may occur in the brain of subjects affected by Alzheimer's disease (AD) and MCP-1 levels in plasma and cerebrospinal fluid have been proposed as biological markers for the inflammatory process that accompanies AD pathogenesis. Importantly, serum levels and biological activity of MCP-1 protein are strongly influenced by a single nucleotide polymorphism occurring at position -2518 of the MCP-1 gene promoter. A recent study has investigated the possible association between this gene polymorphism and AD in a Spanish population, with negative results. Here, we performed a case-control study to test whether the risk for AD might be influenced by the -2518 A/G polymorphism of the MCP-1 gene in an ethnically homogeneous Italian population. The GG genotype and the G allele of the MCP-1 gene polymorphism were significantly more common in the AD group than in control individuals (P<0.0001) A logistic regression analysis indicated that the GG genotype was an independent risk factor for AD in our population. This effect was not influenced by the presence of the APOE 4 high-risk allele, nor by the presence of other gene variations associated with a pro-inflammatory phenotype. These findings indicate that the -2518 A/G polymorphism of the MCP-1 gene is associated with AD in Italians and confirm that inflammatory gene variations may be important contributors in the development and progression of neurodegenerative disorders.
单核细胞趋化蛋白-1(MCP-1)是单核细胞趋化和组织外渗以及炎症期间白细胞功能调节的关键分子。阿尔茨海默病(AD)患者大脑中可能会出现MCP-1上调,血浆和脑脊液中的MCP-1水平已被提议作为伴随AD发病机制的炎症过程的生物学标志物。重要的是,MCP-1蛋白的血清水平和生物学活性受到MCP-1基因启动子-2518位单个核苷酸多态性的强烈影响。最近一项研究调查了西班牙人群中该基因多态性与AD之间的可能关联,结果为阴性。在此,我们进行了一项病例对照研究,以测试在种族同质的意大利人群中,AD风险是否可能受到MCP-1基因-2518 A/G多态性的影响。MCP-1基因多态性的GG基因型和G等位基因在AD组中比对照组个体显著更常见(P<0.0001)。逻辑回归分析表明,GG基因型是我们人群中AD的独立危险因素。这种效应不受APOE 4高风险等位基因的存在影响,也不受与促炎表型相关的其他基因变异的存在影响。这些发现表明,MCP-1基因的-2518 A/G多态性与意大利人的AD相关,并证实炎症基因变异可能是神经退行性疾病发生和发展的重要因素。