4.7 Article

Alterations of nasal microbiome in eosinophilic chronic rhinosinusitis

期刊

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
卷 151, 期 5, 页码 1286-+

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MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2022.11.031

关键词

Chronic rhinosinusitis; eosinophilic chronic rhinosinusitis with nasal polyps; microbiota; nasal microbiome; predictive classifier

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This study aimed to investigate the dysbiosis of nasal microbiome in patients with eosinophilic chronic rhinosinusitis with nasal polyps (eCRSwNP). The results show that the nasal microbiome of eCRSwNP patients has higher a-diversity and a distinct composition of microbes. These differences can be used to distinguish eCRSwNP patients from healthy controls, suggesting the potential of using the nasal microbiota as a noninvasive predictive classifier for the diagnosis of eCRSwNP.
Background: Exposure to microbes may be important in the development of chronic rhinosinusitis (CRS). Dysbiosis of the nasal microbiome is considered to be related to CRS with nasal polyps (CRSwNP). The link between the nasal microbiota and eosinophilic CRSwNP (eCRSwNP) has rarely been studied.Objective: The aim of this study was to rigorously characterize nasal dysbiosis in a cohort of patients with eCRSwNP and compare the nasal microbiomes of these patients with those of healthy controls (HCs). Methods: We performed a cross-sectional study of 34 patients with eCRSwNP, 10 patients without CRSwNP, and 44 HCs by using 16S rRNA gene sequencing. An independent cohort of 14 patients with eCRSwNP, 9 patients without CRSwNP, and 11 HCs was used to validate the results.Results: Compared with the nasal microbiome of healthy controls, the nasal microbiome of patients with eCRSwNP was characterized by higher a-diversity (Shannon and Chao1 index) and a distinct composition of microbes. Notably, the distinct differences in microbial composition between patients with eCRSwNP and HCs were significantly correlated with eCRSwNP disease status. Furthermore, in a diagnostic model generated by using these differences, a combination of 15 genera could be used to distinguish patients with eCRSwNP from HCs, with an area under the curve of approximately 0.8 in both the exploration and validation cohorts. Conclusion: Our study establishes the compositional alterations in the nasal microbiome in eCRSwNP and suggests the potential for using the nasal microbiota as a noninvasive predictive classifier for the diagnosis of eCRSwNP. (J Allergy Clin Immunol 2023;151:1286-95.)

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