慢性阻塞性肺病患者的肠道微生物群因 CT 验证的肺气肿状态而异。

IF 1.8 Q3 RESPIRATORY SYSTEM
European Clinical Respiratory Journal Pub Date : 2025-02-26 eCollection Date: 2025-01-01 DOI:10.1080/20018525.2025.2470499
Anders Ørskov Rotevatn, Tomas Mikal Eagan, Solveig Tangedal, Gunnar Reksten Husebø, Kristoffer Ostridge, Rune Nielsen
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引用次数: 0

摘要

背景和目的:肠道微生物群与慢性阻塞性肺病(COPD)表型的关系尚未得到充分探索。我们旨在比较慢性阻塞性肺病患者和非慢性阻塞性肺病患者的粪便样本,并将研究结果与肺气肿状态、恶化率、血液中嗜酸性粒细胞水平、症状评分和肺功能联系起来:我们报告了一项单中心病例对照研究的结果,研究对象包括 62 名慢性阻塞性肺病患者和 49 名非慢性阻塞性肺病患者。我们从粪便样本中提取了 DNA,并对细菌 16S-rRNA 基因的 V3V4 区域进行了测序。根据胸部计算机断层扫描(CT 胸部)低衰减区≥/结果界定肺气肿:与未患慢性阻塞性肺病的对照组相比,慢性阻塞性肺病患者的 Veillonella 属减少,而属于梭状芽孢杆菌类的一个属增加。与对照组相比,肺气肿患者的微生物组成(β多样性)有所不同,有27个属在肺气肿与对照组中的含量不同。其中九个属属于漆树科。肺功能、血细胞计数和慢性阻塞性肺病评估测试得分与一些属的相对丰富度相关。结论:慢性阻塞性肺病患者的肠道微生物群与肺功能密切相关:结论:慢性阻塞性肺病患者的肠道微生物群与健康人不同,在肺气肿患者中更是如此。结论:慢性阻塞性肺病患者的肠道微生物群与健康人不同,在肺气肿患者中更是如此。未来的研究应特别关注影响漆树科菌群失调的机制和治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gut microbiota in chronic obstructive pulmonary disease varies by CT-verified emphysema status.

Background and aim: The association of the gut microbiota to chronic obstructive pulmonary disease (COPD) phenotypes is underexplored. We aimed to compare stool samples from patients with COPD and subjects without COPD and relate findings to emphysema status, exacerbation rate, blood eosinophil levels, symptom score, and lung function.

Methods: We report findings from a single-centre case-control study with 62 current and former smoking patients with COPD and 49 subjects without COPD. DNA was extracted from stool samples, and the V3V4-region of the bacterial 16S-rRNA gene was sequenced. Emphysema was defined based on thoracic computed tomography (CT thorax) low attenuating areas ≥/<10% at threshold -950 and -910 hounsfield units, respectively. Differential abundance of taxa was evaluated using Analysis of Composition of Microbes with Bias Correction (ANCOM-BC). Beta diversity was compared using a distance-based permanova-test.

Results: The genus Veillonella was decreased and a genus belonging to class Clostridia was increased in COPD compared with controls without COPD. The composition of microbes (beta diversity) differed in emphysema compared to controls, and 27 genera were differentially abundant in emphysema vs. controls. Nine of these genera belonged to the family Lachnospiraceae. Lung function, blood counts and COPD assessment test score correlated with several genera's relative abundance. Of the genera showing significant correlation to lung function, nine belonged to the family Lachnospiraceae.

Conclusion: The gut microbiota in COPD differs from that in healthy individuals, even more so in emphysema. In particular, future studies should look into the mechanisms and therapeutic potential of dysbiosis affecting the family Lachnospiraceae.

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来源期刊
CiteScore
3.80
自引率
0.00%
发文量
15
审稿时长
16 weeks
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