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阿尔茨海默病和路易体痴呆中的一氧化氮合酶基因多态性。

Nitric oxide synthase gene polymorphisms in Alzheimer's disease and dementia with Lewy bodies.

作者信息

Singleton A B, Gibson A M, McKeith I G, Ballard C G, Edwardson J A, Morris C M

机构信息

CAMRC Building, Institute for the Health of the Elderly, Newcastle General Hospital, Westgate Road, Newcastle upon Tyne, UK.

出版信息

Neurosci Lett. 2001 Apr 27;303(1):33-6. doi: 10.1016/s0304-3940(01)01694-9.

Abstract

Evidence suggests that vascular and inflammatory components may be important in the aetiology of dementia and genetic risk factors affecting these processes may therefore influence disease development. Recently, polymorphisms in the endothelial constitutive nitric oxide synthase 3 (NOS3) and also the inducible nitric oxide synthase gene (NOS2A) have been suggested to lead to increased risk of Alzheimer's disease (AD) or dementia with Lewy bodies. We have studied the relationship of both these NOS gene polymorphisms to development of AD and dementia with Lewy bodies and find no evidence for association with either condition. We conclude that NOS gene polymorphisms do not alter disease risk in the majority of late-onset dementia cases.

摘要

有证据表明,血管和炎症成分在痴呆症的病因中可能起重要作用,因此影响这些过程的遗传风险因素可能会影响疾病的发展。最近,有人提出内皮型一氧化氮合酶3(NOS3)和诱导型一氧化氮合酶基因(NOS2A)的多态性会导致患阿尔茨海默病(AD)或路易体痴呆的风险增加。我们研究了这两种NOS基因多态性与AD和路易体痴呆发展之间的关系,未发现与任何一种疾病相关的证据。我们得出结论,在大多数晚发性痴呆病例中,NOS基因多态性不会改变疾病风险。

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