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本文引用的文献

1
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Cureus. 2024 May 21;16(5):e60779. doi: 10.7759/cureus.60779. eCollection 2024 May.
2
Association between modifiable lifestyle pattern and periodontitis: a cross-sectional study based on NHANES.基于 NHANES 的横断面研究:生活方式可调节模式与牙周炎的关系。
BMC Oral Health. 2024 May 21;24(1):591. doi: 10.1186/s12903-024-04207-8.
3
Associated factors of periodontitis and predicted study among young man in China: a population-based cross-sectional study.中国年轻人牙周炎的相关因素及预测研究:一项基于人群的横断面研究。
BMC Public Health. 2024 May 4;24(1):1235. doi: 10.1186/s12889-024-18732-2.
4
Exploring the bi-directional relationship between periodontitis and dyslipidemia: a comprehensive systematic review and meta-analysis.探讨牙周炎与血脂异常的双向关系:全面的系统评价和荟萃分析。
BMC Oral Health. 2024 Apr 29;24(1):508. doi: 10.1186/s12903-023-03668-7.
5
Lipotoxicity: The missing link between diabetes and periodontitis?脂毒性:糖尿病与牙周炎之间缺失的环节?
J Periodontal Res. 2024 Jun;59(3):431-445. doi: 10.1111/jre.13242. Epub 2024 Feb 28.
6
The expression levels of chemotaxis-related molecules CXC chemokine receptor 1, interleukin-8, and pro-platelet basic protein in gingival tissues.牙龈组织中趋化相关分子CXC趋化因子受体1、白细胞介素-8和前血小板碱性蛋白的表达水平。
J Dent Sci. 2024 Jan;19(1):58-63. doi: 10.1016/j.jds.2023.05.031. Epub 2023 Jun 14.
7
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8
Systemic Metabolic Signatures of Oral Diseases.口腔疾病的系统性代谢特征。
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9
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基于机器学习和生物信息学分析的脂肪酸代谢相关基因在牙周炎中的作用。

Role of fatty acid metabolism-related genes in periodontitis based on machine learning and bioinformatics analysis.

机构信息

Stomatological Hospital of Kunming Medical University, Kunming 650000, China.

Yunnan Provincial Key Laboratory of Stomatology, Kunming 650000, China.

出版信息

Hua Xi Kou Qiang Yi Xue Za Zhi. 2024 Dec 1;42(6):735-747. doi: 10.7518/hxkq.2024.2024214.

DOI:10.7518/hxkq.2024.2024214
PMID:39610070
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11669931/
Abstract

OBJECTIVES

This study aims to investigate the role of genes related to fatty acid metabolism in periodontitis through machine learning and bioinformatics methods.

METHODS

Periodontitis datasets GSE10334 and GSE-16134 were downloaded from the GEO database, and the fatty acid metabolism-related gene sets were obtained from the GeneCards database. Differentially expressed fatty acid metabolism-related genes (DEFAMRGs) in periodontitis were screened using the "limma" R package. Functional enrichment and pathway analyses were conducted. Recursive Feature Elimination, Least Absolute Shrinkage and Selection Operator, and Boruta algorithm were used to determine hub DEFAMRGs and construct diagnostic models with internal and external validation. Subtypes of periodontitis related to hub DEFAMRGs were constructed using consistency clustering analysis. CIBERSORT was used to analyze immune cell infiltration in gingival tissues and explore the correlation between hub DEFAMRGs and immune cells.

RESULTS

A total of 113 periodontitis DEFAMRGs were screened out as a result. The enrichment analysis results indicate that DEFAMRGs are mainly associated with immune inflammatory responses and immune cell chemotaxis.Finally, 8 hub DEFAMRGs (BTG2, CXCL12, FABP4, CLDN10, PPBP, RGS1, LGALSL, and RIF1) were identified and a diagnostic model (AUC=0.967) was constructed, based on which periodontitis was divided into two subtypes. In addition, there is a significant correlation between hub DEFAMRGs and different immune cell populations, with mast cells and dendritic cells showing higher correlation.

CONCLUSIONS

This study provides new insights and ideas for the occurrence and development mechanism of periodontitis and proposes a diagnostic model based on hub DEFAMRGs to provide new directions for diagnosis and treatment.

摘要

目的

本研究旨在通过机器学习和生物信息学方法研究与脂肪酸代谢相关的基因在牙周炎中的作用。

方法

从 GEO 数据库中下载牙周炎数据集 GSE10334 和 GSE-16134,从 GeneCards 数据库中获取脂肪酸代谢相关基因集。使用“limma”R 包筛选牙周炎中差异表达的脂肪酸代谢相关基因(DEFAMRGs)。进行功能富集和通路分析。采用递归特征消除、最小绝对值收缩和选择算子以及 Boruta 算法确定枢纽 DEFAMRGs,并进行内部和外部验证构建诊断模型。使用一致性聚类分析构建与枢纽 DEFAMRGs 相关的牙周炎亚型。使用 CIBERSORT 分析牙龈组织中的免疫细胞浸润情况,并探讨枢纽 DEFAMRGs 与免疫细胞的相关性。

结果

共筛选出 113 个牙周炎 DEFAMRGs。富集分析结果表明,DEFAMRGs 主要与免疫炎症反应和免疫细胞趋化有关。最后,确定了 8 个枢纽 DEFAMRGs(BTG2、CXCL12、FABP4、CLDN10、PPBP、RGS1、LGALSL 和 RIF1),并构建了一个诊断模型(AUC=0.967),基于该模型将牙周炎分为两个亚型。此外,枢纽 DEFAMRGs 与不同的免疫细胞群之间存在显著相关性,其中肥大细胞和树突状细胞相关性更高。

结论

本研究为牙周炎的发生发展机制提供了新的见解和思路,提出了基于枢纽 DEFAMRGs 的诊断模型,为诊断和治疗提供了新的方向。