No association between Glu298Asp endothelial nitric oxide synthase polymorphism and Italian sporadic Alzheimer's disease

被引:22
作者
Monastero, R
Cefalù, AB
Camarda, C
Buglino, CM
Mannino, M
Barbagallo, CM
Lopez, G
Camarda, LKC
Travali, S
Camarda, R [1 ]
Averna, MR
机构
[1] Univ Palermo, Inst Neuropsychiat, Ctr Aging Brain & Dementia, Dept Neurol & Rehabil, Palermo, Italy
[2] Univ Palermo, Dept Internal Med, I-90129 Palermo, Italy
[3] Univ Catania, Dept Biomed Sci, Sect Clin Pathol & Mol Oncol, Catania, Italy
关键词
Alzheimer's disease; nitric oxide synthase 3 (NOS3); polymorphism; apolipoprotein E; case-control study;
D O I
10.1016/S0304-3940(03)00210-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A great amount of evidence suggests that neuroinflammation may be a major pathogenetic mechanism in the pathophysiology of sporadic Alzheimer's Disease (sAD). Recently, polymorphisms in the endothelial nitric oxide synthase (NOS3) gene have been associated to late onset Alzheimer's Disease in a British population. However, other groups failed to replicate this finding in Asiatic and Caucasian populations. We conducted a case-control study including a clinically well-defined group of 149 sAD patients and 149 age and sex matched controls to test the association between NOS3 Glu298Asp polymorphism and sAD in an ethnically homogenous Italian population. All subjects were genotyped at NOS3 and apolipoprotein E. No significant difference was found in either allele or genotype frequencies between cases and controls, even after stratification for Apolipoprotein E4 carrier status. The NOS3 Glu298Asp polymorphism does not appear to influence the risk of developing sAD in an Italian population. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:229 / 232
页数:4
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