全基因组差异气道基因表达分析鉴定与COPD合并症相关的基因

IF 4.6 2区 医学 Q1 RESPIRATORY SYSTEM
Lung Pub Date : 2025-04-26 DOI:10.1007/s00408-025-00814-6
Alen Faiz, Else A M D Ter Haar, Jorine E Hartman, Corry-Anke Brandsma, Wim Timens, Janette K Burgess, David F Choy, Michele A Grimbaldeston, Lowie E G W Vanfleteren, Dirk-Jan Slebos, Maarten van den Berge, Simon D Pouwels
{"title":"全基因组差异气道基因表达分析鉴定与COPD合并症相关的基因","authors":"Alen Faiz, Else A M D Ter Haar, Jorine E Hartman, Corry-Anke Brandsma, Wim Timens, Janette K Burgess, David F Choy, Michele A Grimbaldeston, Lowie E G W Vanfleteren, Dirk-Jan Slebos, Maarten van den Berge, Simon D Pouwels","doi":"10.1007/s00408-025-00814-6","DOIUrl":null,"url":null,"abstract":"<p><p>Chronic obstructive pulmonary disease (COPD) is often associated with the co-occurrence of extra-pulmonary diseases, yet the underlying pathophysiology of comorbidities is poorly understood. In COPD patients, the bronchial epithelium often displays cellular damage and is chronically inflamed. The current study aimed to identify differentially expressed genes in bronchial epithelium of COPD patients with and without comorbidities. To this end, a genome-wide differential gene expression analysis was performed on bronchial epithelial samples of 123 severe COPD patients with and without the following comorbidities: anxiety, atherosclerosis, depression, hypercholesterolemia, hypertension, muscle wasting, osteoporosis, and low BMI. COPD patients with osteoporosis displayed higher expression of COL6A3 and lower expression of PHEX. Furthermore, COPD patients with hypercholesterolemia displayed a distinct bronchial epithelial gene expression profile, with 162 differentially expressed genes. No differentially expressed genes were identified for the other comorbidities. This study identified differentially expressed bronchial epithelial genes associated with osteoporosis and hypercholesterolemia in COPD patients.</p>","PeriodicalId":18163,"journal":{"name":"Lung","volume":"203 1","pages":"58"},"PeriodicalIF":4.6000,"publicationDate":"2025-04-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12033178/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genome-Wide Differential Airway Gene Expression Analysis Identifies Genes Associated with COPD Comorbidities.\",\"authors\":\"Alen Faiz, Else A M D Ter Haar, Jorine E Hartman, Corry-Anke Brandsma, Wim Timens, Janette K Burgess, David F Choy, Michele A Grimbaldeston, Lowie E G W Vanfleteren, Dirk-Jan Slebos, Maarten van den Berge, Simon D Pouwels\",\"doi\":\"10.1007/s00408-025-00814-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Chronic obstructive pulmonary disease (COPD) is often associated with the co-occurrence of extra-pulmonary diseases, yet the underlying pathophysiology of comorbidities is poorly understood. In COPD patients, the bronchial epithelium often displays cellular damage and is chronically inflamed. The current study aimed to identify differentially expressed genes in bronchial epithelium of COPD patients with and without comorbidities. To this end, a genome-wide differential gene expression analysis was performed on bronchial epithelial samples of 123 severe COPD patients with and without the following comorbidities: anxiety, atherosclerosis, depression, hypercholesterolemia, hypertension, muscle wasting, osteoporosis, and low BMI. COPD patients with osteoporosis displayed higher expression of COL6A3 and lower expression of PHEX. Furthermore, COPD patients with hypercholesterolemia displayed a distinct bronchial epithelial gene expression profile, with 162 differentially expressed genes. No differentially expressed genes were identified for the other comorbidities. This study identified differentially expressed bronchial epithelial genes associated with osteoporosis and hypercholesterolemia in COPD patients.</p>\",\"PeriodicalId\":18163,\"journal\":{\"name\":\"Lung\",\"volume\":\"203 1\",\"pages\":\"58\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-04-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12033178/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Lung\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s00408-025-00814-6\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"RESPIRATORY SYSTEM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lung","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00408-025-00814-6","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0

摘要

慢性阻塞性肺疾病(COPD)通常与肺外疾病的共发有关,但其潜在的病理生理机制尚不清楚。在COPD患者中,支气管上皮常表现为细胞损伤和慢性炎症。目前的研究旨在鉴定有或无合并症COPD患者支气管上皮中差异表达的基因。为此,研究人员对123例伴有或不伴有以下合并症的重度COPD患者的支气管上皮样本进行了全基因组差异基因表达分析:焦虑、动脉粥样硬化、抑郁、高胆固醇血症、高血压、肌肉萎缩、骨质疏松和低BMI。COPD合并骨质疏松患者COL6A3表达升高,PHEX表达降低。此外,COPD合并高胆固醇血症患者表现出明显的支气管上皮基因表达谱,有162个差异表达基因。其他合并症未发现差异表达基因。本研究确定了COPD患者与骨质疏松症和高胆固醇血症相关的差异表达支气管上皮基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome-Wide Differential Airway Gene Expression Analysis Identifies Genes Associated with COPD Comorbidities.

Chronic obstructive pulmonary disease (COPD) is often associated with the co-occurrence of extra-pulmonary diseases, yet the underlying pathophysiology of comorbidities is poorly understood. In COPD patients, the bronchial epithelium often displays cellular damage and is chronically inflamed. The current study aimed to identify differentially expressed genes in bronchial epithelium of COPD patients with and without comorbidities. To this end, a genome-wide differential gene expression analysis was performed on bronchial epithelial samples of 123 severe COPD patients with and without the following comorbidities: anxiety, atherosclerosis, depression, hypercholesterolemia, hypertension, muscle wasting, osteoporosis, and low BMI. COPD patients with osteoporosis displayed higher expression of COL6A3 and lower expression of PHEX. Furthermore, COPD patients with hypercholesterolemia displayed a distinct bronchial epithelial gene expression profile, with 162 differentially expressed genes. No differentially expressed genes were identified for the other comorbidities. This study identified differentially expressed bronchial epithelial genes associated with osteoporosis and hypercholesterolemia in COPD patients.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Lung
Lung 医学-呼吸系统
CiteScore
9.10
自引率
10.00%
发文量
95
审稿时长
6-12 weeks
期刊介绍: Lung publishes original articles, reviews and editorials on all aspects of the healthy and diseased lungs, of the airways, and of breathing. Epidemiological, clinical, pathophysiological, biochemical, and pharmacological studies fall within the scope of the journal. Case reports, short communications and technical notes can be accepted if they are of particular interest.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信