• 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

一种基于自收缩映射神经网络和图论定义散发性肌萎缩侧索硬化症中赋予风险或保护作用的基因/单核苷酸多态性的新型数学方法。

A Novel Mathematical Approach to Define the Genes/SNPs Conferring Risk or Protection in Sporadic Amyotrophic Lateral Sclerosis Based on Auto Contractive Map Neural Networks and Graph Theory.

作者信息

Buscema Massimo, Penco Silvana, Grossi Enzo

机构信息

Semeion Research Center, Via Sersale 117, 00128 Rome, Italy.

出版信息

Neurol Res Int. 2012;2012:478560. doi: 10.1155/2012/478560. Epub 2012 Aug 9.

DOI:10.1155/2012/478560
PMID:22934166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3425858/
Abstract

Background. Complex diseases like amyotrophic lateral sclerosis (ALS) implicate phenotypic and genetic heterogeneity. Therefore, multiple genetic traits may show differential association with the disease. The Auto Contractive Map (AutoCM), belonging to the Artificial Neural Network (ANN) architecture, "spatializes" the correlation among variables by constructing a suitable embedding space where a visually transparent and cognitively natural notion such as "closeness" among variables reflects accurately their associations. Results. In this pilot case-control study single nucleotide polymorphism (SNP) in several genes has been evaluated with a novel data mining approach based on an AutoCM. We have divided the ALS dataset into two dataset: Cases and Control dataset; we have applied to each one, independently, the AutoCM algorithm. Six genetic variants were identified which differently contributed to the complexity of the system: three of the above genes/SNPs represent protective factors, APOA4, NOS3, and LPL, since their contribution to the whole complexity resulted to be as high as 0.17. On the other hand ADRB3, LIPC, and MMP3, whose hub relevancies contribution resulted to be as high as 0.13, seem to represent susceptibility factors. Conclusion. The biological information available on these six polymorphisms is consistent with possible pathogenetic pathways related to ALS.

摘要

背景。像肌萎缩侧索硬化症(ALS)这样的复杂疾病涉及表型和遗传异质性。因此,多种遗传特征可能与该疾病呈现不同的关联。自动收缩映射(AutoCM)属于人工神经网络(ANN)架构,通过构建一个合适的嵌入空间来“空间化”变量之间的相关性,在这个空间中,诸如变量之间“接近度”这样视觉上透明且认知上自然的概念能准确反映它们之间的关联。结果。在这项初步的病例对照研究中,使用了基于AutoCM的新型数据挖掘方法对多个基因中的单核苷酸多态性(SNP)进行了评估。我们将ALS数据集分为两个数据集:病例数据集和对照数据集;我们分别独立地对每个数据集应用了AutoCM算法。鉴定出六个对系统复杂性有不同贡献的基因变异:上述三个基因/SNP代表保护因素,即载脂蛋白A4(APOA4)、一氧化氮合酶3(NOS3)和脂蛋白脂肪酶(LPL),因为它们对整体复杂性的贡献高达0.17。另一方面,β3肾上腺素能受体(ADRB3)、肝脂酶(LIPC)和基质金属蛋白酶3(MMP3),其中心相关性贡献高达0.13,似乎代表易感性因素。结论。关于这六种多态性的生物学信息与ALS可能的致病途径一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/ff76e044daa6/NRI2012-478560.alg.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/5e43fdf525b1/NRI2012-478560.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/93337143c3ce/NRI2012-478560.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/13d7394c988a/NRI2012-478560.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/ff76e044daa6/NRI2012-478560.alg.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/5e43fdf525b1/NRI2012-478560.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/93337143c3ce/NRI2012-478560.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/13d7394c988a/NRI2012-478560.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27b4/3425858/ff76e044daa6/NRI2012-478560.alg.001.jpg

相似文献

1
A Novel Mathematical Approach to Define the Genes/SNPs Conferring Risk or Protection in Sporadic Amyotrophic Lateral Sclerosis Based on Auto Contractive Map Neural Networks and Graph Theory.一种基于自收缩映射神经网络和图论定义散发性肌萎缩侧索硬化症中赋予风险或保护作用的基因/单核苷酸多态性的新型数学方法。
Neurol Res Int. 2012;2012:478560. doi: 10.1155/2012/478560. Epub 2012 Aug 9.
2
Gene-gene and gene - clinical factors interaction in acute myocardial infarction: a new detailed risk chart.基因-基因和基因-临床因素相互作用与急性心肌梗死:一个新的详细风险图表。
Curr Pharm Des. 2010;16(7):783-8. doi: 10.2174/138161210790883543.
3
Artificial neural networks help to identify disease subsets and to predict lymphoma in primary Sjögren's syndrome.人工神经网络有助于识别疾病亚群并预测原发性干燥综合征中的淋巴瘤。
Clin Exp Rheumatol. 2018 May-Jun;36 Suppl 112(3):137-144. Epub 2018 Aug 14.
4
New application of intelligent agents in sporadic amyotrophic lateral sclerosis identifies unexpected specific genetic background.智能代理在散发性肌萎缩侧索硬化症中的新应用识别出意外的特定遗传背景。
BMC Bioinformatics. 2008 May 30;9:254. doi: 10.1186/1471-2105-9-254.
5
Data Mining of Determinants of Intrauterine Growth Retardation Revisited Using Novel Algorithms Generating Semantic Maps and Prototypical Discriminating Variable Profiles.使用生成语义图和原型判别变量概况的新算法对宫内生长迟缓的决定因素进行再数据挖掘。
PLoS One. 2015 Jul 9;10(7):e0126020. doi: 10.1371/journal.pone.0126020. eCollection 2015.
6
Whole-genome analysis of sporadic amyotrophic lateral sclerosis.散发性肌萎缩侧索硬化症的全基因组分析
N Engl J Med. 2007 Aug 23;357(8):775-88. doi: 10.1056/NEJMoa070174. Epub 2007 Aug 1.
7
Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.肌萎缩侧索硬化症中的拷贝数变异:通过系统生物学方法拼凑马赛克。
Mol Neurobiol. 2018 Feb;55(2):1299-1322. doi: 10.1007/s12035-017-0393-x. Epub 2017 Jan 24.
8
Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosis.全基因组分析显示,患肌萎缩侧索硬化症不一致的同卵双胞胎之间不存在致病的单核苷酸或结构差异。
Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(5-6):385-92. doi: 10.3109/21678421.2015.1040029. Epub 2015 May 11.
9
Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen.散发性肌萎缩侧索硬化症中的拷贝数变异:全基因组筛查
Lancet Neurol. 2008 Apr;7(4):319-26. doi: 10.1016/S1474-4422(08)70048-6. Epub 2008 Mar 3.
10
Difficulty in determining the association of a single nucleotide polymorphism in the ZNF512B gene with the risk and prognosis of amyotrophic lateral sclerosis.确定ZNF512B基因中的单核苷酸多态性与肌萎缩侧索硬化症的风险和预后之间的关联存在困难。
Rinsho Shinkeigaku. 2017 Aug 31;57(8):417-424. doi: 10.5692/clinicalneurol.cn-001032. Epub 2017 Jul 22.

引用本文的文献

1
Apolipoprotein A (ApoA) in Neurological Disorders: Connections and Insights.载脂蛋白A(ApoA)在神经系统疾病中的关联与见解
Int J Mol Sci. 2025 Aug 16;26(16):7908. doi: 10.3390/ijms26167908.
2
Networks in Coronary Heart Disease Genetics As a Step towards Systems Epidemiology.冠心病遗传学中的网络:迈向系统流行病学的一步
PLoS One. 2015 May 7;10(5):e0125876. doi: 10.1371/journal.pone.0125876. eCollection 2015.
3
Biomarkers in autism spectrum disorder: the old and the new.自闭症谱系障碍中的生物标志物:新旧之辨。

本文引用的文献

1
In vitro effects of cholesterol β-D-glucoside, cholesterol and cycad phytosterol glucosides on respiration and reactive oxygen species generation in brain mitochondria.胆固醇 β-D-葡萄糖苷、胆固醇和苏铁植物固醇葡萄糖苷对脑线粒体呼吸和活性氧生成的体外影响。
J Membr Biol. 2010 Oct;237(2-3):71-7. doi: 10.1007/s00232-010-9307-9. Epub 2010 Oct 12.
2
Lipid molecules induce the cytotoxic aggregation of Cu/Zn superoxide dismutase with structurally disordered regions.脂质分子诱导具有结构无序区域的铜/锌超氧化物歧化酶发生细胞毒性聚集。
Biochim Biophys Acta. 2011 Jan;1812(1):41-8. doi: 10.1016/j.bbadis.2010.09.003. Epub 2010 Sep 15.
3
Psychopharmacology (Berl). 2014 Mar;231(6):1201-16. doi: 10.1007/s00213-013-3290-7. Epub 2013 Oct 6.
4
Application of artificial neural networks to investigate one-carbon metabolism in Alzheimer's disease and healthy matched individuals.应用人工神经网络研究阿尔茨海默病患者和健康匹配个体的一碳代谢。
PLoS One. 2013 Aug 12;8(8):e74012. doi: 10.1371/journal.pone.0074012. eCollection 2013.
Amyotrophic lateral sclerosis.
肌萎缩侧索硬化症。
Adv Exp Med Biol. 2010;685:9-20. doi: 10.1007/978-1-4419-6448-9_2.
4
The role of oxidative stress in amyotrophic lateral sclerosis and Parkinson's disease.氧化应激在肌萎缩侧索硬化症和帕金森病中的作用。
Neurochem Res. 2010 Oct;35(10):1530-7. doi: 10.1007/s11064-010-0212-5. Epub 2010 Jun 10.
5
Amyotrophic lateral sclerosis, physical exercise, trauma and sports: results of a population-based pilot case-control study.肌萎缩侧索硬化症、体育锻炼、创伤与运动:一项基于人群的试点病例对照研究结果
Amyotroph Lateral Scler. 2010 May 3;11(3):289-92. doi: 10.3109/17482960903384283.
6
Lower serum lipid levels are related to respiratory impairment in patients with ALS.较低的血脂水平与肌萎缩侧索硬化症患者的呼吸功能损害有关。
Neurology. 2009 Nov 17;73(20):1681-5. doi: 10.1212/WNL.0b013e3181c1df1e.
7
Implication of beta3-adrenoceptors in the antidepressant-like effects of amibegron using Adrb3 knockout mice in the chronic mild stress.β3-肾上腺素能受体在慢性轻度应激中阿米贝隆抗抑郁样作用中的意义:利用 Adrb3 基因敲除小鼠的研究
Behav Brain Res. 2010 Jan 20;206(2):310-2. doi: 10.1016/j.bbr.2009.09.003. Epub 2009 Sep 8.
8
Hepatic lipase promoter C-480T polymorphism is associated with serum lipids levels, but not subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study.肝脂肪酶启动子C-480T多态性与血脂水平相关,但与亚临床动脉粥样硬化无关:芬兰青年人心血管风险研究
Clin Genet. 2009 Jul;76(1):46-53. doi: 10.1111/j.1399-0004.2009.01180.x. Epub 2009 Jun 22.
9
Trp64Arg polymorphism in ADRB3 gene is associated with elite endurance performance.ADRB3 基因中的 Trp64Arg 多态性与精英耐力表现有关。
Br J Sports Med. 2011 Feb;45(2):147-9. doi: 10.1136/bjsm.2009.061366. Epub 2009 Jun 23.
10
Genetic studies of amyotrophic lateral sclerosis: controversies and perspectives.肌萎缩侧索硬化症的遗传学研究:争议与展望
Amyotroph Lateral Scler. 2009 Feb;10(1):1-14. doi: 10.1080/17482960802585469.