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Genetic study of Sardinian patients with Alzheimer's disease.

机译:撒丁岛阿尔茨海默氏病患者的遗传研究。

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摘要

We describe the genetic analysis of an Alzheimer's disease (AD) sample derived from a genetically isolated population. Genetic assessment included the analysis of genes involved in AD, such as the genes for amyloid precursor protein (APP), presenilin 1 (PSEN1) and presenilin 2 (PSEN2). We also assessed genes for some proteins that constitute the gamma-secretase complex: nicastrin (NCSTN), presenilin enhancer-2 (PEN2), in addition to the AD risk factor apolipoprotein E (APOE). Using polymerase chain reaction and single strand conformational polymorphism method, screens for APP, PSEN1 and PSEN2 genes revealed one mutation in PSEN1. Furthermore, we found an intronic +17G>C polymorphism in PEN2 which, in homozygous form, was greater in early onset Alzheimer's disease (EOAD) compared to controls, and one haplotype in the NCSTN gene which was linked to EOAD and familial AD (FAD). Finally, the genotyping of APOE confirmed that the varepsilon4 allele could be a risk factor for the onset of AD, in particular for FAD subjects. In conclusion, these results show the existence of Sardinian genetic peculiarities, essential in studies regarding genetically inherited and multifactorial disorders, as AD.
机译:我们描述了遗传分离人群中的阿尔茨海默氏病(AD)样本的遗传分析。遗传评估包括对AD相关基因的分析,例如淀粉样蛋白前体蛋白(APP),早老素1(PSEN1)和早老素2(PSEN2)的基因。我们还评估了构成γ-分泌酶复合物的某些蛋白质的基因:尼卡斯汀(NCSTN),早老素增强子2(PEN2),以及AD危险因子载脂蛋白E(APOE)。使用聚合酶链反应和单链构象多态性方法,对APP,PSEN1和PSEN2基因的筛选揭示了PSEN1中的一个突变。此外,我们在PEN2中发现内含+ 17G> C多态性,纯合型在早发性阿尔茨海默氏病(EOAD)中比对照组更大,并且在NCSTN基因中有一个单倍型与EOAD和家族性AD(FAD)相关)。最后,APOE的基因分型证实了varepsilon4等位基因可能是AD发作的危险因素,特别是对于FAD受试者。总之,这些结果表明了撒丁岛遗传特性的存在,这在有关遗传性遗传和多因素疾病(AD)研究中必不可少。

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