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本文引用的文献

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Role of cyclooxygenase-2 and 5-lipoxygenase polymorphisms in Alzheimer's disease in a population from northern Italy: implication for pharmacogenomics.环氧化酶-2 和 5-脂氧合酶多态性在意大利北部人群阿尔茨海默病中的作用:对药物基因组学的启示。
J Alzheimers Dis. 2010;19(2):551-7. doi: 10.3233/JAD-2010-1260.
2
Association of plasma leptin levels with incident Alzheimer disease and MRI measures of brain aging.血浆瘦素水平与阿尔茨海默病发病及脑老化 MRI 测量指标的相关性。
JAMA. 2009 Dec 16;302(23):2565-72. doi: 10.1001/jama.2009.1836.
3
Phenomics: the systematic study of phenotypes on a genome-wide scale.表型组学:在全基因组范围内对表型进行系统研究。
Neuroscience. 2009 Nov 24;164(1):30-42. doi: 10.1016/j.neuroscience.2009.01.027. Epub 2009 Jan 20.
4
Arrowsmith two-node search interface: a tutorial on finding meaningful links between two disparate sets of articles in MEDLINE.阿罗史密斯双节点搜索界面:关于在医学在线数据库(MEDLINE)中两组不同文章之间寻找有意义联系的教程。
Comput Methods Programs Biomed. 2009 May;94(2):190-7. doi: 10.1016/j.cmpb.2008.12.006. Epub 2009 Jan 30.
5
Increased 5-lipoxygenase immunoreactivity in the hippocampus of patients with Alzheimer's disease.阿尔茨海默病患者海马体中5-脂氧合酶免疫反应性增加。
J Histochem Cytochem. 2008 Dec;56(12):1065-73. doi: 10.1369/jhc.2008.951855. Epub 2008 Aug 4.
6
Identification of ALOX5 as a gene regulating adiposity and pancreatic function.鉴定ALOX5作为一种调节肥胖和胰腺功能的基因。
Diabetologia. 2008 Jun;51(6):978-88. doi: 10.1007/s00125-008-1002-3. Epub 2008 Apr 18.
7
5-Lipoxygenase gene disruption reduces amyloid-beta pathology in a mouse model of Alzheimer's disease.5-脂氧合酶基因敲除可减轻阿尔茨海默病小鼠模型中的β-淀粉样蛋白病理改变。
FASEB J. 2008 Apr;22(4):1169-78. doi: 10.1096/fj.07-9131.com. Epub 2007 Nov 12.

神经精神疾病表型组学的益处:以5-脂氧合酶-瘦素-阿尔茨海默病关联为例。

Benefits of neuropsychiatric phenomics: example of the 5-lipoxygenase-leptin-Alzheimer connection.

作者信息

Manev Hari, Manev Radmila

机构信息

Department of Psychiatry, University of Illinois at Chicago, Chicago, IL 60612, USA.

出版信息

Cardiovasc Psychiatry Neurol. 2010;2010:838164. doi: 10.1155/2010/838164. Epub 2010 Jun 27.

DOI:10.1155/2010/838164
PMID:20672007
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2905908/
Abstract

Phenomics is a systematic study of phenotypes on a genomewide scale that is expected to unravel, as of yet, unsuspected functional roles of the genome. It remains to be determined how to optimally approach and analyze the available phenomics databases to spearhead innovation in neuropsychiatry. By serendipitously connecting two unrelated phenotypes of increased blood levels of the adipokine leptin, a molecule that regulates appetite, in 5-lipoxygenase- (5-LOX) deficient mice and patients with a lower risk for Alzheimer's disease (AD), we postulated a leptin-mediated basis for beneficial effects of ALOX5 (a gene encoding 5-LOX) gene-deficiency in AD. We suggest that it might be possible to avoid relying on serendipity and develop data-mining tools capable of extracting from phenomics databases indications for such novel hypotheses. Hence, we provide an example of using a free-access Arrowsmith two-node search interface to identify ALOX5 as unsuspected putative mechanisms for the previously described clinical association between increased plasma levels of leptin and a lower risk of incident dementia and AD.

摘要

表型组学是在全基因组范围内对表型进行的系统研究,有望揭示基因组尚未被怀疑的功能作用。如何以最佳方式处理和分析现有的表型组学数据库以引领神经精神病学的创新仍有待确定。通过意外地将两种不相关的表型联系起来,即脂肪因子瘦素(一种调节食欲的分子)血液水平升高在5-脂氧合酶(5-LOX)缺陷小鼠和患阿尔茨海默病(AD)风险较低的患者中的表现,我们推测了ALOX5(一种编码5-LOX的基因)基因缺陷在AD中产生有益作用的瘦素介导基础。我们认为有可能避免依赖偶然性,开发能够从表型组学数据库中提取此类新假设线索的数据挖掘工具。因此,我们提供了一个使用免费访问的Arrowsmith双节点搜索界面的例子,以确定ALOX5是先前描述的瘦素血浆水平升高与痴呆症和AD发病风险降低之间临床关联的未被怀疑的潜在机制。