载脂蛋白E基因型与老年挪威队列阿尔茨海默病

Benjamin R. , Leake A. , McArthur F.K. , Candy J.M. , Ince P.G. , Edwardson J.A. , Torvik A. , Morris C.M. , Bjertness E.
{"title":"载脂蛋白E基因型与老年挪威队列阿尔茨海默病","authors":"Benjamin R. ,&nbsp;Leake A. ,&nbsp;McArthur F.K. ,&nbsp;Candy J.M. ,&nbsp;Ince P.G. ,&nbsp;Edwardson J.A. ,&nbsp;Torvik A. ,&nbsp;Morris C.M. ,&nbsp;Bjertness E.","doi":"10.1006/neur.1996.0006","DOIUrl":null,"url":null,"abstract":"<div><p>Apolipoprotein E (Apo E) genotyping was performed on an autopsy cohort of neuropathologically verified non-demented controls and subjects with Alzheimer's disease (AD) resident in nursing homes in the Oslo area. AD was associated with a significantly increased frequency of the Apo E ϵ4 allele; the frequency of the ϵ2 and ϵ3 alleles was lower in AD but not significantly so. Age at death in the control group and the AD group did not differ significantly; neither did age at death nor age at onset of dementia in AD vary according to Apo E genotype, though tendencies towards an earlier age at death was seen in individuals with ϵ4/4 and earlier age at onset dementia in the presence of an ϵ4 allele and a later age of onset the presence of an ϵ3 allele were seen. Possession of an ϵ2 allele had no effect on age at onset of dementia or age at death. Among the possible genotypes there was a trend towards a progression of earliest onset ϵ4/4, ϵ2/4, ϵ3/4, ϵ3/3, ϵ2/3 latest onset of dementia and longest duration ϵ2/4, ϵ4/4, ϵ3/4, ϵ3/3, ϵ2/3 to shortest duration of dementia.</p></div>","PeriodicalId":19127,"journal":{"name":"Neurodegeneration","volume":"5 1","pages":"Pages 43-47"},"PeriodicalIF":0.0000,"publicationDate":"1996-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1006/neur.1996.0006","citationCount":"9","resultStr":"{\"title\":\"Apolipoprotein E Genotype and Alzheimer's Disease in an Elderly Norwegian Cohort\",\"authors\":\"Benjamin R. ,&nbsp;Leake A. ,&nbsp;McArthur F.K. ,&nbsp;Candy J.M. ,&nbsp;Ince P.G. ,&nbsp;Edwardson J.A. ,&nbsp;Torvik A. ,&nbsp;Morris C.M. ,&nbsp;Bjertness E.\",\"doi\":\"10.1006/neur.1996.0006\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Apolipoprotein E (Apo E) genotyping was performed on an autopsy cohort of neuropathologically verified non-demented controls and subjects with Alzheimer's disease (AD) resident in nursing homes in the Oslo area. AD was associated with a significantly increased frequency of the Apo E ϵ4 allele; the frequency of the ϵ2 and ϵ3 alleles was lower in AD but not significantly so. Age at death in the control group and the AD group did not differ significantly; neither did age at death nor age at onset of dementia in AD vary according to Apo E genotype, though tendencies towards an earlier age at death was seen in individuals with ϵ4/4 and earlier age at onset dementia in the presence of an ϵ4 allele and a later age of onset the presence of an ϵ3 allele were seen. Possession of an ϵ2 allele had no effect on age at onset of dementia or age at death. Among the possible genotypes there was a trend towards a progression of earliest onset ϵ4/4, ϵ2/4, ϵ3/4, ϵ3/3, ϵ2/3 latest onset of dementia and longest duration ϵ2/4, ϵ4/4, ϵ3/4, ϵ3/3, ϵ2/3 to shortest duration of dementia.</p></div>\",\"PeriodicalId\":19127,\"journal\":{\"name\":\"Neurodegeneration\",\"volume\":\"5 1\",\"pages\":\"Pages 43-47\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1996-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1006/neur.1996.0006\",\"citationCount\":\"9\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neurodegeneration\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1055833096900069\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurodegeneration","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1055833096900069","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 9

摘要

载脂蛋白E (Apo E)基因分型对奥斯陆地区养老院中经神经病理学证实的非痴呆对照组和阿尔茨海默病(AD)患者的尸检队列进行。AD与载脂蛋白E ϵ4等位基因频率显著增加有关;ϵ2和ϵ3等位基因的频率在AD患者中较低,但差异不显著。对照组与AD组死亡年龄差异无统计学意义;随着载脂蛋白E基因型的不同,AD患者的死亡年龄和痴呆发病年龄也没有变化,尽管在存在ϵ4等位基因的ϵ4/4和痴呆发病年龄较早的个体中发现了死亡年龄的趋势,并且在存在ϵ3等位基因的个体中发现了发病年龄较晚的趋势。拥有ϵ2等位基因对痴呆发病年龄或死亡年龄没有影响。可能的基因型之间有一个趋势发展的早期发病ϵ4/4,ϵ2/4,ϵ3/4,ϵ3/3,ϵ2/3最新出现痴呆和最长时间ϵ2/4,ϵ4/4,ϵ3/4,ϵ3/3,ϵ2/3痴呆的最短时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Apolipoprotein E Genotype and Alzheimer's Disease in an Elderly Norwegian Cohort

Apolipoprotein E (Apo E) genotyping was performed on an autopsy cohort of neuropathologically verified non-demented controls and subjects with Alzheimer's disease (AD) resident in nursing homes in the Oslo area. AD was associated with a significantly increased frequency of the Apo E ϵ4 allele; the frequency of the ϵ2 and ϵ3 alleles was lower in AD but not significantly so. Age at death in the control group and the AD group did not differ significantly; neither did age at death nor age at onset of dementia in AD vary according to Apo E genotype, though tendencies towards an earlier age at death was seen in individuals with ϵ4/4 and earlier age at onset dementia in the presence of an ϵ4 allele and a later age of onset the presence of an ϵ3 allele were seen. Possession of an ϵ2 allele had no effect on age at onset of dementia or age at death. Among the possible genotypes there was a trend towards a progression of earliest onset ϵ4/4, ϵ2/4, ϵ3/4, ϵ3/3, ϵ2/3 latest onset of dementia and longest duration ϵ2/4, ϵ4/4, ϵ3/4, ϵ3/3, ϵ2/3 to shortest duration of dementia.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Behavioural Problems in Dementia and Biochemistry: Clinical Aspects Neurochemical Correlates of Dementia Amyloid Precursor Protein mRNAs in Alzheimer's Disease Structural Correlates of Cognition in Dementia: Quantification and Assessment of Synapse Change Pyramidal Nerve Cell Loss in Alzheimer's Disease
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1