{"title":"Stage-Associated Subgingival Dysbiosis Across the Periodontal Disease Spectrum in a Thai Cohort","authors":"Teerat Sawangpanyangkura, Kanokphong Suparan, Chanyanuch Wechwithayakhlung, Chanon Kunasol, Nipon Chattipakorn, Siriporn C. Chattipakorn","doi":"10.1111/jcpe.70147","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Aims</h3>\n \n <p>This cross-sectional study aimed to investigate the subgingival microbiota and predict functional profiles across the 2018 EFP/AAP periodontal disease spectrum in a Thai clinical cohort.</p>\n </section>\n \n <section>\n \n <h3> Materials and Methods</h3>\n \n <p>Subgingival plaque from 100 participants (gingivitis, <i>n</i> = 30; Stage II–IV periodontitis, <i>n</i> = 70) was analysed by 16S rRNA gene sequencing with taxonomic assignment using the Human Oral Microbiome Database.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p><i>Peptostreptococcaceae</i>-related taxa, <i>Dialister pneumosintes</i>, <i>Shuttleworthia satelles</i>, <i>Prevotella</i> sp. HMT-304, and Bacteroidetes [G-3] bacterium HMT-280 were recurrently identified across differential abundance and penalised regression analyses. Penalised regression models showed limited stage-discriminative performance (multinomial AUC 0.68–0.78), with gingivitis achieving the highest classification accuracy (63%) and Stage IV the lowest, consistent with overlapping microbial profiles across stages. Nonetheless, some stage-enriched taxa included <i>Campylobacter</i> species in Stage III and <i>Porphyromonas gingivalis</i> with <i>Odoribacter</i> bacterium HMT-516 in Stage IV. Stage-enriched taxa correlated with anaerobic fermentation pathways, while co-occurrence networks became less dense but broader across stages.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Stage-associated microbiome shifts were detectable using a gingivitis reference group, with a disease-associated core and accompanying anaerobic functional enrichment. The findings suggest that subgingival dysbiosis across periodontitis stages does not follow a simple linear trajectory and that clinical stage is not determined by microbiome composition alone.</p>\n </section>\n </div>","PeriodicalId":15380,"journal":{"name":"Journal of Clinical Periodontology","volume":"53 8","pages":"1332-1343"},"PeriodicalIF":8.3000,"publicationDate":"2026-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Periodontology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jcpe.70147","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/5/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0
Abstract
Aims
This cross-sectional study aimed to investigate the subgingival microbiota and predict functional profiles across the 2018 EFP/AAP periodontal disease spectrum in a Thai clinical cohort.
Materials and Methods
Subgingival plaque from 100 participants (gingivitis, n = 30; Stage II–IV periodontitis, n = 70) was analysed by 16S rRNA gene sequencing with taxonomic assignment using the Human Oral Microbiome Database.
Results
Peptostreptococcaceae-related taxa, Dialister pneumosintes, Shuttleworthia satelles, Prevotella sp. HMT-304, and Bacteroidetes [G-3] bacterium HMT-280 were recurrently identified across differential abundance and penalised regression analyses. Penalised regression models showed limited stage-discriminative performance (multinomial AUC 0.68–0.78), with gingivitis achieving the highest classification accuracy (63%) and Stage IV the lowest, consistent with overlapping microbial profiles across stages. Nonetheless, some stage-enriched taxa included Campylobacter species in Stage III and Porphyromonas gingivalis with Odoribacter bacterium HMT-516 in Stage IV. Stage-enriched taxa correlated with anaerobic fermentation pathways, while co-occurrence networks became less dense but broader across stages.
Conclusion
Stage-associated microbiome shifts were detectable using a gingivitis reference group, with a disease-associated core and accompanying anaerobic functional enrichment. The findings suggest that subgingival dysbiosis across periodontitis stages does not follow a simple linear trajectory and that clinical stage is not determined by microbiome composition alone.
期刊介绍:
Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology.
The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope.
The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.