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Meta-Analysis
. 2024 May 8:15:1407439.
doi: 10.3389/fimmu.2024.1407439. eCollection 2024.

The alterations of oral, airway and intestine microbiota in chronic obstructive pulmonary disease: a systematic review and meta-analysis

Affiliations
Meta-Analysis

The alterations of oral, airway and intestine microbiota in chronic obstructive pulmonary disease: a systematic review and meta-analysis

Ziwei Kou et al. Front Immunol. .

Abstract

Background: Increasing evidence indicates the microbial ecology of chronic obstructive pulmonary disease (COPD) is intricately associated with the disease's status and severity, and distinct microbial ecological variations exist between COPD and healthy control (HC). This systematic review and meta-analysis aimed to summarize microbial diversity indices and taxa relative abundance of oral, airway, and intestine microbiota of different stages of COPD and HC to make comparisons.

Methods: A comprehensive systematic literature search was conducted in PubMed, Embase, the Web of Science, and the Cochrane Library databases to identify relevant English articles on the oral, airway, and intestine microbiota in COPD published between 2003 and 8 May 2023. Information on microbial diversity indices and taxa relative abundance of oral, airway, and intestine microbiota was collected for comparison between different stages of COPD and HC.

Results: A total of 20 studies were included in this review, involving a total of 337 HC participants, 511 COPD patients, and 154 AECOPD patients. We observed that no significant differences in alpha diversity between the participant groups, but beta diversity was significantly different in half of the included studies. Compared to HC, Prevotella, Streptococcus, Actinomyces, and Veillonella of oral microbiota in SCOPD were reduced at the genus level. Most studies supported that Haemophilus, Lactobacillus, and Pseudomonas were increased, but Veillonella, Prevotella, Actinomyces, Porphyromonas, and Atopobium were decreased at the genus level in the airway microbiota of SCOPD. However, the abundance of Haemophilus, Lactobacillus and Pseudomonas genera exhibited an increase, whereas Actinomyces and Porphyromonas showed a decrease in the airway microbiota of AECOPD compared to HC. And Lachnospira of intestine microbiota in SCOPD was reduced at the genus level.

Conclusion: The majority of published research findings supported that COPD exhibited decreased alpha diversity compared to HC. However, our meta-analysis does not confirm it. In order to further investigate the characteristics and mechanisms of microbiome in the oral-airway- intestine axis of COPD patients, larger-scale and more rigorous studies are needed.

Systematic review registration: PROSPERO (https://www.crd.york.ac.uk/prospero/), identifier CRD42023418726.

Keywords: alpha-diversity; beta-diversity; chronic obstructive respiratory disease; human airway microbiome; human intestine microbiome; human oral microbiome; meta-analysis; relative abundance.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Quality score of included articles calculated using the NOS.
Figure 2
Figure 2
PRISMA flow diagram of selected studies for inclusion.
Figure 3
Figure 3
Forest plot of randomized controlled trials comparing the oral microbial alpha-diversity between HC and SCOPD. (A) Chao 1 index; (B) Shannon index.
Figure 4
Figure 4
Forest plot of randomized controlled trials comparing the airway microbial alpha-diversity among HC, SCOPD and AECOPD. (A) Chao 1 index; (B) Richness; (C) Shannon index; (D) Simpson index.
Figure 5
Figure 5
Taxa relative abundance changes in microbiota between SCOPD and AECOPD compared to HC. (A) The oral genus comparison of taxa relative abundance between HC and SCOPD. (B) The intestinal genus comparison of taxa relative abundance between HC and SCOPD. (C) The airway phyla comparison of taxa relative abundance between SCOPD and AECOPD compared to HC. (D) The airway genus comparison of taxa relative abundance between SCOPD and AECOPD compared to HC.

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References

    1. Adeloye D, Song P, Zhu Y, Campbell H, Sheikh A, Rudan I. Global, regional, and national prevalence of, and risk factors for, chronic obstructive pulmonary disease (COPD) in 2019: a systematic review and modelling analysis. Lancet Respir Med. (2022) 10:447–58. doi: 10.1016/S2213-2600(21)00511-7 - DOI - PMC - PubMed
    1. Wang C, Xu J, Yang L, Xu Y, Zhang X, Bai C, et al. . Prevalence and risk factors of chronic obstructive pulmonary disease in China (the China Pulmonary Health [CPH] study): a national cross-sectional study. Lancet. (2018) 391:1706–17. doi: 10.1016/S0140-6736(18)30841-9 - DOI - PubMed
    1. Belkaid Y, Harrison OJ. Homeostatic immunity and the microbiota. Immunity. (2017) 46:562–76. doi: 10.1016/j.immuni.2017.04.008 - DOI - PMC - PubMed
    1. Belkaid Y, Hand TW. Role of the microbiota in immunity and inflammation. Cell. (2014) 157:121–41. doi: 10.1016/j.cell.2014.03.011 - DOI - PMC - PubMed
    1. Wang L, Cai Y, Garssen J, Henricks PAJ, Folkerts G, Braber S. The bidirectional gut-lung axis in chronic obstructive pulmonary disease. Am J Respir Crit Care Med. (2023) 207:1145–60. doi: 10.1164/rccm.202206-1066TR - DOI - PMC - PubMed