从糖尿病到痴呆症:识别认知障碍发展过程中的关键基因》(From Diabetes to Dementia: Identifying Key Genes in the Progression of Cognitive Impairment)。

IF 2.7 3区 医学 Q3 NEUROSCIENCES
Zhaoming Cao, Yage Du, Guangyi Xu, He Zhu, Yinchao Ma, Ziyuan Wang, Shaoying Wang, Yanhui Lu
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引用次数: 0

摘要

研究目的采用两种生物信息学方法筛选参与轻度认知障碍(MCI)和2型糖尿病进展的关键基因,为进一步研究2型糖尿病相关轻度认知障碍(DCI)的分子机制提供依据:方法:从GEO数据库下载MCI组和正常认知组的RNA测序数据,以及GSE63060(包含160个MCI样本和104个正常样本)的临床特征数据的表达谱和样本信息数据。利用加权基因共表达网络分析(WGCNA)确定了枢纽基因。蛋白质-蛋白质相互作用(PPI)分析结合最小绝对收缩和选择算子(LASSO)和接收者操作特征曲线(ROC)分析用于验证基因。此外,我们还从 GEO 数据库中下载了 13 例 2 型糖尿病样本和 13 例正常对照的 GSE166502 RNA 测序和临床特征数据,并通过差异和 ROC 曲线分析验证了筛选出的基因与 2 型糖尿病之间的相关性。此外,我们还收集了临床活检样本以验证结果:结果:基于WGCNA,我们整合了10个模块,其中6个模块与MCI相关。使用 LASSO 算法确定了 6 个与 MCI 相关的中心基因(TOMM7、SNRPG、COX7C、UQCRQ、RPL31 和 RPS24)。通过整合 GEO 数据库筛选出的 ROC 曲线显示,COX7C、SNRPG、TOMM7 和 RPS24 是 2 型糖尿病进展的关键基因:结论:COX7C、SNRPG、TOMM7和RPS24参与了MCI和2型糖尿病的进展。结论:COX7C、SNRPG、TOMM7 和 RPS24 参与了 MCI 和 2 型糖尿病的进展,因此,应研究这四个基因在 2 型糖尿病相关 MCI 发展过程中的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Diabetes to Dementia: Identifying Key Genes in the Progression of Cognitive Impairment.

Objectives: To provide a basis for further research on the molecular mechanisms underlying type 2 diabetes-associated mild cognitive impairment (DCI) using two bioinformatics methods to screen key genes involved in the progression of mild cognitive impairment (MCI) and type 2 diabetes.

Methods: RNA sequencing data of MCI and normal cognition groups, as well as expression profile and sample information data of clinical characteristic data of GSE63060, which contains 160 MCI samples and 104 normal samples, were downloaded from the GEO database. Hub genes were identified using weighted gene co-expression network analysis (WGCNA). Protein-protein interaction (PPI) analysis, combined with least absolute shrinkage and selection operator (LASSO) and receiver operating characteristic (ROC) curve analyses, was used to verify the genes. Moreover, RNA sequencing and clinical characteristic data for GSE166502 of 13 type 2 diabetes samples and 13 normal controls were downloaded from the GEO database, and the correlation between the screened genes and type 2 diabetes was verified by difference and ROC curve analyses. In addition, we collected clinical biopsies to validate the results.

Results: Based on WGCNA, 10 modules were integrated, and six were correlated with MCI. Six hub genes associated with MCI (TOMM7, SNRPG, COX7C, UQCRQ, RPL31, and RPS24) were identified using the LASSO algorithm. The ROC curve was screened by integrating the GEO database, and revealed COX7C, SNRPG, TOMM7, and RPS24 as key genes in the progression of type 2 diabetes.

Conclusions: COX7C, SNRPG, TOMM7, and RPS24 are involved in MCI and type 2 diabetes progression. Therefore, the molecular mechanisms of these four genes in the development of type 2 diabetes-associated MCI should be studied.

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来源期刊
Brain Sciences
Brain Sciences Neuroscience-General Neuroscience
CiteScore
4.80
自引率
9.10%
发文量
1472
审稿时长
18.71 days
期刊介绍: Brain Sciences (ISSN 2076-3425) is a peer-reviewed scientific journal that publishes original articles, critical reviews, research notes and short communications in the areas of cognitive neuroscience, developmental neuroscience, molecular and cellular neuroscience, neural engineering, neuroimaging, neurolinguistics, neuropathy, systems neuroscience, and theoretical and computational neuroscience. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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