神经精神表型组学的益处:5-脂氧合酶-瘦素-阿尔茨海默病联系的例子。

Cardiovascular psychiatry and neurology Pub Date : 2010-01-01 Epub Date: 2010-06-27 DOI:10.1155/2010/838164
Hari Manev, Radmila Manev
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引用次数: 7

摘要

表型组学是一种在全基因组范围内对表型进行的系统研究,有望解开迄今为止未被怀疑的基因组功能角色。如何最佳地接近和分析可用的表型组学数据库,以引领神经精神病学的创新,仍有待确定。通过在5-脂氧合酶(5-LOX)缺陷小鼠和阿尔茨海默病(AD)风险较低的患者中偶然连接两种不相关的脂肪因子瘦素(一种调节食欲的分子)血液水平升高的表型,我们假设ALOX5(一种编码5-LOX的基因)基因缺乏在AD中有益作用的瘦素介导的基础。我们建议有可能避免依赖于意外发现,并开发能够从表型组学数据库中提取此类新假设适应症的数据挖掘工具。因此,我们提供了一个使用自由访问的Arrowsmith双节点搜索界面的例子,以确定ALOX5是先前描述的血浆瘦素水平升高与痴呆和AD发生率降低之间的临床关联的未经怀疑的假定机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benefits of neuropsychiatric phenomics: example of the 5-lipoxygenase-leptin-Alzheimer connection.

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.

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