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Dementia and geriatric cognitive disorders · 2004

Association of the Neprilysin gene with susceptibility to late-onset Alzheimer's disease.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
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Sakai Ayumu, Ujike Hiroshi, Nakata Kenji, Takehisa Yasushi, Imamura Takaki, Uchida Naohiko, Kanzaki Akihiro, Yamamoto Mitsutoshi, Fujisawa Yoshikatsu, Okumura Kazuya, Kuroda Shigetoshi

Аннотация

Neprilysin (NEP), also known as neutral endopeptidase, enkephalinase, CD 10, and common acute lymphoblastic leukemia antigen, is a 97-kD protein. NEP can degrade amyloid beta peptides, and its mRNA and protein levels are known to be reduced in the brains of patients with Alzheimer's disease (AD), making the NEP gene a substantial candidate for an AD risk factor. We examined the genetic association of three NEP polymorphisms, a GT-repeat polymorphism and two single nucleotide polymorphisms (SNPs, -1075A>G and -1284G>C) in its promoter region, with AD in a Japanese case-control sample (240 patients and 163 controls). The GT-repeat polymorphism, but not the SNPs, was significantly associated with late-onset AD (p = 0.0007). Our findings suggest that the GT-repeat polymorphism in the promoter region of the NEP gene or some other unknown polymorphisms, which are in a linkage disequilibrium, confer a susceptibility to late-onset AD.

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