Salivary microbiome and asthma risk in children with orofacial defects

Background Patients with congenital orofacial defects, cleft lip (CL), cleft palate (CP), and cleft lip and palate (CLP) have continuous exposure of the respiratory system to the microbiome from the oral environment, offering opportunities to develop mucosal immunity in the airway. This two‐part stu...

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Veröffentlicht in:Pediatric pulmonology 2023-10, Vol.58 (10), p.2777-2785
Hauptverfasser: Chen, I‐Lun, Huang, Faye, Li, Sung‐Chou, Huang, Hsin‐Chun
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container_issue 10
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container_title Pediatric pulmonology
container_volume 58
creator Chen, I‐Lun
Huang, Faye
Li, Sung‐Chou
Huang, Hsin‐Chun
description Background Patients with congenital orofacial defects, cleft lip (CL), cleft palate (CP), and cleft lip and palate (CLP) have continuous exposure of the respiratory system to the microbiome from the oral environment, offering opportunities to develop mucosal immunity in the airway. This two‐part study aims to analyze data on asthma occurrence in CL, CP, and CLP infants and the composition of the salivary microbiome, and to evaluate the oral microbiota and its association with the risk of developing childhood asthma. Methods Patient data from the research database of Chang Gung Memorial Hospital from 2004 to 2015 were retrospectively analyzed by multivariable regression. Diseases diagnoses were defined by ICD codes. Asthma must also meet the criteria for receiving selective β2 agonistic or/and inhaled corticosteroid treatments twice within 1 year. Analysis of the saliva microbiome was performed prospectively from 2016 to 2020 in 10 healthy term infants and 10 CLP infants on postnatal 7th day, 1 month, and 6 months by next‐generation sequencing. Results Asthma and nonasthma groups included 988 and 3952 patients, respectively. The incidence of asthma development was higher in patients with CP than in CL and CLP groups (aOR: 5.644, CI: 1.423–22.376). The species composition of the microbiome at 1 and 6 months was significantly different between infants with CLP and healthy infants. Conclusion Children with orofacial defects have a higher risk of developing asthma with a possible contribution from oral microbiota in the early months of life.
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This two‐part study aims to analyze data on asthma occurrence in CL, CP, and CLP infants and the composition of the salivary microbiome, and to evaluate the oral microbiota and its association with the risk of developing childhood asthma. Methods Patient data from the research database of Chang Gung Memorial Hospital from 2004 to 2015 were retrospectively analyzed by multivariable regression. Diseases diagnoses were defined by ICD codes. Asthma must also meet the criteria for receiving selective β2 agonistic or/and inhaled corticosteroid treatments twice within 1 year. Analysis of the saliva microbiome was performed prospectively from 2016 to 2020 in 10 healthy term infants and 10 CLP infants on postnatal 7th day, 1 month, and 6 months by next‐generation sequencing. Results Asthma and nonasthma groups included 988 and 3952 patients, respectively. The incidence of asthma development was higher in patients with CP than in CL and CLP groups (aOR: 5.644, CI: 1.423–22.376). The species composition of the microbiome at 1 and 6 months was significantly different between infants with CLP and healthy infants. 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This two‐part study aims to analyze data on asthma occurrence in CL, CP, and CLP infants and the composition of the salivary microbiome, and to evaluate the oral microbiota and its association with the risk of developing childhood asthma. Methods Patient data from the research database of Chang Gung Memorial Hospital from 2004 to 2015 were retrospectively analyzed by multivariable regression. Diseases diagnoses were defined by ICD codes. Asthma must also meet the criteria for receiving selective β2 agonistic or/and inhaled corticosteroid treatments twice within 1 year. Analysis of the saliva microbiome was performed prospectively from 2016 to 2020 in 10 healthy term infants and 10 CLP infants on postnatal 7th day, 1 month, and 6 months by next‐generation sequencing. Results Asthma and nonasthma groups included 988 and 3952 patients, respectively. The incidence of asthma development was higher in patients with CP than in CL and CLP groups (aOR: 5.644, CI: 1.423–22.376). The species composition of the microbiome at 1 and 6 months was significantly different between infants with CLP and healthy infants. Conclusion Children with orofacial defects have a higher risk of developing asthma with a possible contribution from oral microbiota in the early months of life.</description><subject>Asthma</subject><subject>atopic diseases</subject><subject>children</subject><subject>lung diseases</subject><subject>Microbiota</subject><subject>oral microbiome</subject><subject>orofacial defects</subject><issn>8755-6863</issn><issn>1099-0496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kMtKAzEUQIMotlY3foAE3IgwNY_JJLOUYlUoWNCuh3TmhqbOoyYzlv69qVNduHAVLjkc7j0IXVIypoSwu82mK8csEYodoSElaRqROE2O0VBJIaJEJXyAzrxfExL-UnqKBlzGklBKhmj6qkv7qd0OVzZ3zdI2FWBdF1j7dlVp7Kx_x7bG-cqWhYMab227wo1rjM6tLnEBBvLWn6MTo0sPF4d3hBbTh7fJUzR7eXye3M-inAvJIl4wAoxyGgsmlaCKEk245AqE1EswlAkAwhOpc6MV1aCNKooiFiYPA2g-Qje9d-Oajw58m1XW51CWuoam8xlTMWFxHMQBvf6DrpvO1WG7QCUpZVRKEajbngrHe-_AZBtnq9AjoyTb1832dbPvugG-Oii7ZQXFL_qTMwC0B7a2hN0_qmw-X8x66RdpK4Rm</recordid><startdate>202310</startdate><enddate>202310</enddate><creator>Chen, I‐Lun</creator><creator>Huang, Faye</creator><creator>Li, Sung‐Chou</creator><creator>Huang, Hsin‐Chun</creator><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6585-6809</orcidid><orcidid>https://orcid.org/0000-0003-0571-5956</orcidid></search><sort><creationdate>202310</creationdate><title>Salivary microbiome and asthma risk in children with orofacial defects</title><author>Chen, I‐Lun ; Huang, Faye ; Li, Sung‐Chou ; Huang, Hsin‐Chun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3572-3d20e21314527851810a03738e57abef125ee0367acfa81aeaf8ddd45fc1aeea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Asthma</topic><topic>atopic diseases</topic><topic>children</topic><topic>lung diseases</topic><topic>Microbiota</topic><topic>oral microbiome</topic><topic>orofacial defects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, I‐Lun</creatorcontrib><creatorcontrib>Huang, Faye</creatorcontrib><creatorcontrib>Li, Sung‐Chou</creatorcontrib><creatorcontrib>Huang, Hsin‐Chun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatric pulmonology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, I‐Lun</au><au>Huang, Faye</au><au>Li, Sung‐Chou</au><au>Huang, Hsin‐Chun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Salivary microbiome and asthma risk in children with orofacial defects</atitle><jtitle>Pediatric pulmonology</jtitle><addtitle>Pediatr Pulmonol</addtitle><date>2023-10</date><risdate>2023</risdate><volume>58</volume><issue>10</issue><spage>2777</spage><epage>2785</epage><pages>2777-2785</pages><issn>8755-6863</issn><eissn>1099-0496</eissn><abstract>Background Patients with congenital orofacial defects, cleft lip (CL), cleft palate (CP), and cleft lip and palate (CLP) have continuous exposure of the respiratory system to the microbiome from the oral environment, offering opportunities to develop mucosal immunity in the airway. This two‐part study aims to analyze data on asthma occurrence in CL, CP, and CLP infants and the composition of the salivary microbiome, and to evaluate the oral microbiota and its association with the risk of developing childhood asthma. Methods Patient data from the research database of Chang Gung Memorial Hospital from 2004 to 2015 were retrospectively analyzed by multivariable regression. Diseases diagnoses were defined by ICD codes. Asthma must also meet the criteria for receiving selective β2 agonistic or/and inhaled corticosteroid treatments twice within 1 year. Analysis of the saliva microbiome was performed prospectively from 2016 to 2020 in 10 healthy term infants and 10 CLP infants on postnatal 7th day, 1 month, and 6 months by next‐generation sequencing. Results Asthma and nonasthma groups included 988 and 3952 patients, respectively. The incidence of asthma development was higher in patients with CP than in CL and CLP groups (aOR: 5.644, CI: 1.423–22.376). The species composition of the microbiome at 1 and 6 months was significantly different between infants with CLP and healthy infants. Conclusion Children with orofacial defects have a higher risk of developing asthma with a possible contribution from oral microbiota in the early months of life.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>37470110</pmid><doi>10.1002/ppul.26582</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-6585-6809</orcidid><orcidid>https://orcid.org/0000-0003-0571-5956</orcidid></addata></record>
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source Wiley Online Library Journals Frontfile Complete
subjects Asthma
atopic diseases
children
lung diseases
Microbiota
oral microbiome
orofacial defects
title Salivary microbiome and asthma risk in children with orofacial defects
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