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阿尔茨海默病和额颞叶痴呆患者中不存在TREM2基因多态性。

Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration.

作者信息

Fenoglio Chiara, Galimberti Daniela, Piccio Laura, Scalabrini Diego, Panina Paola, Buonsanti Cecilia, Venturelli Eliana, Lovati Carlo, Forloni Gianluigi, Mariani Claudio, Bresolin Nereo, Scarpini Elio

机构信息

Department of Neurological Sciences, "Dino Ferrari" Center, University of Milan, IRCCS Fondazione Ospedale Maggiore Policlinico, Milan, Italy.

出版信息

Neurosci Lett. 2007 Jan 10;411(2):133-7. doi: 10.1016/j.neulet.2006.10.029. Epub 2006 Nov 7.

Abstract

Triggering Receptor Expressed on Myeloid cells (TREM)2 deficiency originates a genetic syndrome characterized by bone cysts and presenile dementia, named Nasu-Hakola disease (NHD). Early onset dementia and marked involvement of frontal regions are features characterizing both NHD and other kinds of neurodegenerative disorders, such as Frontotemporal Lobar Degeneration (FTLD), and, in some cases, Alzheimer's disease (AD). Three Single Nucleotide Polymorphisms (SNPs) in TREM2 coding region were screened by allelic discrimination in a population of probable AD patients as well as FTLD patients as compared with age-matched controls. In addition, mutation scanning of the coding region of TREM2 gene was carried out in 7 patients with early onset AD (EOAD), 16 FTLD, and 20 controls. None of the SNPs analyzed was present, either in patients or controls. Moreover, mutation scanning of the five exons of TREM2 failed to detect the presence of novel polymorphisms. These data demonstrate that TREM2 coding region is highly conserved, implying a crucial role of this receptor. Further studies, including a functional analysis, are certainly required to clarify the role of TREM2 in neurodegenerative processes.

摘要

髓系细胞表达触发受体(TREM)2缺乏会引发一种以骨囊肿和早老性痴呆为特征的遗传综合征,称为纳苏 - 哈科拉病(NHD)。早发性痴呆和额叶区域的明显受累是NHD以及其他类型神经退行性疾病(如额颞叶痴呆(FTLD))的特征,在某些情况下,也是阿尔茨海默病(AD)的特征。通过等位基因鉴别,在一群可能患有AD的患者以及FTLD患者中,与年龄匹配的对照组相比,筛查了TREM2编码区域中的三个单核苷酸多态性(SNP)。此外,对7例早发性AD(EOAD)患者、16例FTLD患者和20例对照进行了TREM2基因编码区域的突变扫描。分析的SNP在患者或对照中均未出现。此外,TREM2五个外显子的突变扫描未能检测到新的多态性。这些数据表明TREM2编码区域高度保守,这意味着该受体具有关键作用。当然,需要进一步的研究,包括功能分析,以阐明TREM2在神经退行性过程中的作用。

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