• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

No association between DCP1 genotype and late-onset Alzheimer disease.

作者信息

Buss Svenja, Müller-Thomsen Tomas, Hock Cristoph, Alberici Antonella, Binetti Giuliano, Nitsch Roger M, Gal Andreas, Finckh Ulrich

机构信息

Department of Human Genetics, University Hospital Hamburg-Eppendorf, University of Hamburg, Hamburg, Germany.

出版信息

Am J Med Genet. 2002 May 8;114(4):440-5. doi: 10.1002/ajmg.10306.

DOI:10.1002/ajmg.10306
PMID:11992568
Abstract

In a study of 261 patients with Alzheimer disease (AD) and 306 cognitively normal control subjects from Germany, Switzerland, and Italy, we found no association between genotype counts or allelic frequencies of DCP1, the gene encoding angiotensin-converting enzyme. In accordance with several other studies, our data could not confirm previous association findings. Critical review about all studies available on DCP1 genotyping and AD, age-associated cognitive decline, longevity, and other conditions revealed remarkable inconsistencies. Several studies showed significant deviations of genotype counts from Hardy Weinberg equilibrium (HWE). Deviations from HWE may limit the comparability of study results and require clarification before drawing conclusions with respect to disease risk, health conditions, or longevity in association with DCP1 genotype.

摘要

相似文献

1
No association between DCP1 genotype and late-onset Alzheimer disease.
Am J Med Genet. 2002 May 8;114(4):440-5. doi: 10.1002/ajmg.10306.
2
Association between apolipoprotein E polymorphism and Alzheimer disease in Tehran, Iran.伊朗德黑兰载脂蛋白E基因多态性与阿尔茨海默病之间的关联。
Neurosci Lett. 2005 Feb 25;375(1):1-6. doi: 10.1016/j.neulet.2004.10.073. Epub 2004 Nov 26.
3
Angiotensin converting enzyme insertion/deletion polymorphism in sporadic and familial Alzheimer's disease and longevity.散发性和家族性阿尔茨海默病及长寿中的血管紧张素转换酶插入/缺失多态性
Arch Gerontol Geriatr. 2007 Sep-Oct;45(2):201-6. doi: 10.1016/j.archger.2006.10.011. Epub 2006 Dec 19.
4
Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease.编码血管紧张素转换酶(ACE)的DCP1基因变异与阿尔茨海默病易感性相关。
Nat Genet. 1999 Jan;21(1):71-2. doi: 10.1038/5009.
5
Implication of sex and SORL1 variants in italian patients with Alzheimer disease.性别及SORL1基因变异在意大利阿尔茨海默病患者中的意义
Arch Neurol. 2009 Oct;66(10):1260-6. doi: 10.1001/archneurol.2009.101.
6
APOE is associated with age-of-onset, but not cognitive functioning, in late-life depression.载脂蛋白E与老年抑郁症的发病年龄相关,但与认知功能无关。
Int J Geriatr Psychiatry. 2003 Dec;18(12):1075-81. doi: 10.1002/gps.1006.
7
Increased risk for Alzheimer disease with the interaction of MPO and A2M polymorphisms.MPO与A2M基因多态性相互作用会增加患阿尔茨海默病的风险。
Arch Neurol. 2004 Mar;61(3):341-4. doi: 10.1001/archneur.61.3.341.
8
Association analysis of brain-derived neurotrophic factor (BDNF) gene 196 A/G polymorphism with Alzheimer's disease (AD) in mainland Chinese.中国大陆人群脑源性神经营养因子(BDNF)基因196 A/G多态性与阿尔茨海默病(AD)的关联分析
Neurosci Lett. 2005 Oct 14;387(1):11-6. doi: 10.1016/j.neulet.2005.07.009.
9
Apolipoprotein E genotype and age-related myelin breakdown in healthy individuals: implications for cognitive decline and dementia.健康个体中载脂蛋白E基因型与年龄相关的髓鞘破坏:对认知衰退和痴呆症的影响。
Arch Gen Psychiatry. 2006 Jan;63(1):63-72. doi: 10.1001/archpsyc.63.1.63.
10
Association analysis of methionine synthase gene 2756 A>G polymorphism and Alzheimer disease in a Chinese population.中国人群中甲硫氨酸合成酶基因2756 A>G多态性与阿尔茨海默病的关联分析
Brain Res. 2008 Apr 14;1204:118-22. doi: 10.1016/j.brainres.2008.01.064. Epub 2008 Feb 5.

引用本文的文献

1
Angiotensin-converting enzyme polymorphisms AND Alzheimer's disease susceptibility: An updated meta-analysis.血管紧张素转化酶基因多态性与阿尔茨海默病易感性:一项更新的荟萃分析。
PLoS One. 2021 Nov 24;16(11):e0260498. doi: 10.1371/journal.pone.0260498. eCollection 2021.
2
Angiotensin-converting enzyme insertion/deletion polymorphism is not a major determining factor in the development of sporadic Alzheimer disease: evidence from an updated meta-analysis.血管紧张素转换酶插入/缺失多态性并非散发性阿尔茨海默病发生的主要决定因素:一项更新的荟萃分析证据
PLoS One. 2014 Oct 31;9(10):e111406. doi: 10.1371/journal.pone.0111406. eCollection 2014.
3
Lack of association between angiotensin-converting enzyme and dementia of the Alzheimer's type in an elderly Arab population in Wadi Ara, Israel.
在以色列 Wadi Ara 的老年阿拉伯人群中,血管紧张素转换酶与阿尔茨海默病型痴呆之间缺乏关联。
Neuropsychiatr Dis Treat. 2005 Mar;1(1):73-6. doi: 10.2147/nedt.1.1.73.52302.
4
C677T methylentetrahydrofulate reductase and angiotensin converting enzyme gene polymorphisms in patients with Alzheimer's disease in Iranian population.伊朗人群中阿尔茨海默病患者的C677T亚甲基四氢叶酸还原酶和血管紧张素转换酶基因多态性
Neurochem Res. 2006 Aug;31(8):1079-83. doi: 10.1007/s11064-006-9119-6. Epub 2006 Aug 12.
5
Apolipoprotein E, angiotensin-converting enzyme and kallikrein gene polymorphisms and the risk of Alzheimer's disease and vascular dementia.载脂蛋白E、血管紧张素转换酶和激肽释放酶基因多态性与阿尔茨海默病和血管性痴呆的风险
J Neural Transm (Vienna). 2006 Oct;113(10):1499-509. doi: 10.1007/s00702-005-0424-z. Epub 2006 Feb 9.
6
Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.转铁蛋白的C2等位基因与血色素沉着症基因(HFE)的C282Y等位基因之间的协同作用作为患阿尔茨海默病的风险因素。
J Med Genet. 2004 Apr;41(4):261-5. doi: 10.1136/jmg.2003.015552.
7
Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2.迟发性阿尔茨海默病与位于10q22.2染色体上编码尿激酶型纤溶酶原激活剂的PLAU基因的一种基因型的关联。
Neurogenetics. 2003 Aug;4(4):213-7. doi: 10.1007/s10048-003-0157-9. Epub 2003 Jul 24.