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阿尔茨海默病中胆固醇相关基因的关联研究。

Association study of cholesterol-related genes in Alzheimer's disease.

作者信息

Wollmer M Axel, Sleegers Kristel, Ingelsson Martin, Zekanowski Cezary, Brouwers Nathalie, Maruszak Aleksandra, Brunner Fabienne, Huynh Kim-Dung, Kilander Lena, Brundin Rose-Marie, Hedlund Marie, Giedraitis Vilmantas, Glaser Anna, Engelborghs Sebastiaan, De Deyn Peter P, Kapaki Elisabeth, Tsolaki Magdalini, Daniilidou Makrina, Molyva Dimitra, Paraskevas George P, Thal Dietmar R, Barcikowska Maria, Kuznicki Jacek, Lannfelt Lars, Van Broeckhoven Christine, Nitsch Roger M, Hock Christoph, Papassotiropoulos Andreas

机构信息

Division of Psychiatry Research, University of Zürich, August Forel Str. 1, 8008 Zurich, Switzerland.

出版信息

Neurogenetics. 2007 Aug;8(3):179-88. doi: 10.1007/s10048-007-0087-z. Epub 2007 Mar 27.

Abstract

Alzheimer's disease (AD) is a genetically complex disorder, and several genes related to cholesterol metabolism have been reported to contribute to AD risk. To identify further AD susceptibility genes, we have screened genes that map to chromosomal regions with high logarithm of the odds scores for AD in full genome scans and are related to cholesterol metabolism. In a European screening sample of 115 sporadic AD patients and 191 healthy control subjects, we analyzed single nucleotide polymorphisms in 28 cholesterol-related genes for association with AD. The genes HMGCS2, FDPS, RAFTLIN, ACAD8, NPC2, and ABCG1 were associated with AD at a significance level of P < or = 0.05 in this sample. Replication trials in five independent European samples detected associations of variants within HMGCS2, FDPS, NPC2, or ABCG1 with AD in some samples (P = 0.05 to P = 0.005). We did not identify a marker that was significantly associated with AD in the pooled sample (n = 2864). Stratification of this sample revealed an APOE-dependent association of HMGCS2 with AD (P = 0.004). We conclude that genetic variants investigated in this study may be associated with a moderate modification of the risk for AD in some samples.

摘要

阿尔茨海默病(AD)是一种基因复杂的疾病,据报道,一些与胆固醇代谢相关的基因会增加患AD的风险。为了进一步确定AD易感基因,我们筛选了在全基因组扫描中与AD的优势对数得分高的染色体区域相关且与胆固醇代谢有关的基因。在一个由115名散发性AD患者和191名健康对照者组成的欧洲筛查样本中,我们分析了28个胆固醇相关基因中的单核苷酸多态性与AD的关联性。在该样本中,基因HMGCS2、FDPS、RAFTLIN、ACAD8、NPC2和ABCG1与AD的关联达到了P≤0.05的显著水平。在五个独立的欧洲样本中进行的重复试验在一些样本中检测到HMGCS2、FDPS、NPC2或ABCG1内的变体与AD有关联(P = 0.05至P = 0.005)。我们在合并样本(n = 2864)中未发现与AD显著相关的标记。对该样本进行分层分析发现HMGCS2与AD存在载脂蛋白E(APOE)依赖性关联(P = 0.004)。我们得出结论,本研究中调查的基因变异可能在某些样本中与AD风险的适度改变有关。

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