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Differential role of triggering receptors expressed on myeloid cells 2 R47H in 3 neurodegenerative diseases based on a systematic review and meta-analysis.基于系统评价和Meta分析的髓系细胞触发受体2 R47H在3种神经退行性疾病中的差异作用
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本文引用的文献

1
The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.罕见的TREM2 R47H变体对阿尔茨海默病风险仅产生适度影响。
Neurology. 2014 Oct 7;83(15):1353-8. doi: 10.1212/WNL.0000000000000855. Epub 2014 Sep 3.
2
Investigation of TREM2, PLD3, and UNC5C variants in patients with Alzheimer's disease from mainland China.中国大陆阿尔茨海默病患者中TREM2、PLD3和UNC5C基因变异的研究。
Neurobiol Aging. 2014 Oct;35(10):2422.e9-2422.e11. doi: 10.1016/j.neurobiolaging.2014.04.025. Epub 2014 May 1.
3
Lack of genetic association between TREM2 and late-onset Alzheimer's disease in a Japanese population.在日本人群中,TREM2与晚发型阿尔茨海默病之间缺乏基因关联。
J Alzheimers Dis. 2014;41(4):1031-8. doi: 10.3233/JAD-140225.
4
Association study of TREM2 polymorphism rs75932628 with late-onset Alzheimer's disease in Chinese Han population.中国汉族人群中TREM2基因多态性rs75932628与晚发型阿尔茨海默病的关联研究
Neurol Res. 2014 Oct;36(10):894-6. doi: 10.1179/1743132814Y.0000000376. Epub 2014 Apr 13.
5
Exome array study did not identify novel variants in Alzheimer's disease.外显子组芯片研究未发现阿尔茨海默病的新变异。
Neurobiol Aging. 2014 Aug;35(8):1958.e13-4. doi: 10.1016/j.neurobiolaging.2014.03.007. Epub 2014 Mar 11.
6
Evidence of trem2 variant associated with triple risk of Alzheimer's disease.与阿尔茨海默病三重风险相关的TREM2变体证据。
PLoS One. 2014 Mar 24;9(3):e92648. doi: 10.1371/journal.pone.0092648. eCollection 2014.
7
Missense variant in TREML2 protects against Alzheimer's disease.TREML2基因中的错义变异可预防阿尔茨海默病。
Neurobiol Aging. 2014 Jun;35(6):1510.e19-26. doi: 10.1016/j.neurobiolaging.2013.12.010. Epub 2013 Dec 21.
8
Triggering receptor expressed on myeloid cells 2 variant is rare in late-onset Alzheimer's disease in Han Chinese individuals.髓样细胞表达的触发受体2变体在汉族晚发性阿尔茨海默病患者中罕见。
Neurobiol Aging. 2014 Apr;35(4):937.e1-3. doi: 10.1016/j.neurobiolaging.2013.10.075. Epub 2013 Oct 11.
9
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia.研究罕见杂合性TREM2变异体在阿尔茨海默病和额颞叶痴呆中的作用。
Neurobiol Aging. 2014 Mar;35(3):726.e11-9. doi: 10.1016/j.neurobiolaging.2013.09.009. Epub 2013 Oct 9.
10
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia.评估TREM2基因p.R47H变体作为阿尔茨海默病和额颞叶痴呆风险因素的作用。
Neurobiol Aging. 2014 Feb;35(2):444.e1-4. doi: 10.1016/j.neurobiolaging.2013.08.011. Epub 2013 Sep 13.

东亚人群中TREM2与阿尔茨海默病之间缺乏基因关联:一项系统评价和荟萃分析。

Lack of genetic association between TREM2 and Alzheimer's disease in East Asian population: a systematic review and meta-analysis.

作者信息

Huang Man, Wang Dejun, Xu Zhijun, Xu Yongshan, Xu Xiaoping, Ma Yuefeng, Xia Zheng

机构信息

Department of General Intensive Care Unit, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Am J Alzheimers Dis Other Demen. 2015 Sep;30(6):541-6. doi: 10.1177/1533317515577128.

DOI:10.1177/1533317515577128
PMID:25852195
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10852690/
Abstract

PURPOSE

Large-scale genome-wide association studies have identified TREM2 variants to be significantly associated with Alzheimer's disease (AD) in caucasian population. The goal of this systematic study and meta-analysis was to assess the association between Triggering receptor expressed on myeloid cells 2 (TREM2) variants and AD in East Asian population.

METHODS

In this study, literatures were searched in PubMed, MEDLINE, EMBASE, and the Cochrane library to screen citations from January 1990 to June 2014. Data analysis was done by using the Stata 12 software.

RESULTS

Twelve studies were considered for analysis. A total of 13 535 patients with AD and 22 976 healthy controls were studied. The results showed that rs75932628 variant was significantly associated with AD in caucasian population (P < .001, odds ratio ¼ 3.17, 95% confidence interval 2.45-4.09). However, the association was not found in East Asian population.

CONCLUSION

In our study, we found that TREM2 variant is likely not associated with AD in East Asian population.

摘要

目的

大规模全基因组关联研究已确定髓系细胞触发受体2(TREM2)变异与白种人群中的阿尔茨海默病(AD)显著相关。本系统研究和荟萃分析的目的是评估东亚人群中髓系细胞触发受体2(TREM2)变异与AD之间的关联。

方法

在本研究中,检索了PubMed、MEDLINE、EMBASE和Cochrane图书馆中的文献,以筛选1990年1月至2014年6月的引文。使用Stata 12软件进行数据分析。

结果

共纳入12项研究进行分析。共研究了13535例AD患者和22976例健康对照。结果显示,rs75932628变异在白种人群中与AD显著相关(P <.001,比值比¼ 3.17,95%置信区间2.45 - 4.09)。然而,在东亚人群中未发现这种关联。

结论

在我们的研究中,我们发现TREM2变异在东亚人群中可能与AD无关。