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Oral microbiome variations related to ageing: possible implications beyond oral health
The global population is getting older due to a combination of longer life expectancy and declining birth rates. Growing evidence suggests that the oral microbiota composition and distribution may have a profound effect on how well we age. The purpose of this study was to investigate age-related ora...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016173/ https://www.ncbi.nlm.nih.gov/pubmed/36920536 http://dx.doi.org/10.1007/s00203-023-03464-5 |
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author | Kazarina, Alisa Kuzmicka, Jevgenija Bortkevica, Santa Zayakin, Pawel Kimsis, Janis Igumnova, Viktorija Sadovska, Darja Freimane, Lauma Kivrane, Agnija Namina, Agne Capligina, Valentina Poksane, Alise Ranka, Renate |
author_facet | Kazarina, Alisa Kuzmicka, Jevgenija Bortkevica, Santa Zayakin, Pawel Kimsis, Janis Igumnova, Viktorija Sadovska, Darja Freimane, Lauma Kivrane, Agnija Namina, Agne Capligina, Valentina Poksane, Alise Ranka, Renate |
author_sort | Kazarina, Alisa |
collection | PubMed |
description | The global population is getting older due to a combination of longer life expectancy and declining birth rates. Growing evidence suggests that the oral microbiota composition and distribution may have a profound effect on how well we age. The purpose of this study was to investigate age-related oral microbiome variations of supragingival plaque and buccal mucosa samples in the general population in Latvia. Our results indicated significant difference between supragingival plaque bacterial profiles of three age groups (20–40; 40–60; 60 + years). Within supragingival plaque samples, age group 20–40 showed the highest bacterial diversity with a decline during the 40–60 age period and uprise again after the age of 60. Among other differences, the important oral commensal Neisseria had declined after the age of 40. Additionally, prevalence of two well-documented opportunistic pathogens Streptococcus anginosus and Gemella sanguinis gradually rose with age within our samples. Furthermore, supragingival plaque and buccal mucosa samples significantly differed in overall bacterial composition. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00203-023-03464-5. |
format | Online Article Text |
id | pubmed-10016173 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-100161732023-03-15 Oral microbiome variations related to ageing: possible implications beyond oral health Kazarina, Alisa Kuzmicka, Jevgenija Bortkevica, Santa Zayakin, Pawel Kimsis, Janis Igumnova, Viktorija Sadovska, Darja Freimane, Lauma Kivrane, Agnija Namina, Agne Capligina, Valentina Poksane, Alise Ranka, Renate Arch Microbiol Long Paper The global population is getting older due to a combination of longer life expectancy and declining birth rates. Growing evidence suggests that the oral microbiota composition and distribution may have a profound effect on how well we age. The purpose of this study was to investigate age-related oral microbiome variations of supragingival plaque and buccal mucosa samples in the general population in Latvia. Our results indicated significant difference between supragingival plaque bacterial profiles of three age groups (20–40; 40–60; 60 + years). Within supragingival plaque samples, age group 20–40 showed the highest bacterial diversity with a decline during the 40–60 age period and uprise again after the age of 60. Among other differences, the important oral commensal Neisseria had declined after the age of 40. Additionally, prevalence of two well-documented opportunistic pathogens Streptococcus anginosus and Gemella sanguinis gradually rose with age within our samples. Furthermore, supragingival plaque and buccal mucosa samples significantly differed in overall bacterial composition. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00203-023-03464-5. Springer Berlin Heidelberg 2023-03-15 2023 /pmc/articles/PMC10016173/ /pubmed/36920536 http://dx.doi.org/10.1007/s00203-023-03464-5 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Long Paper Kazarina, Alisa Kuzmicka, Jevgenija Bortkevica, Santa Zayakin, Pawel Kimsis, Janis Igumnova, Viktorija Sadovska, Darja Freimane, Lauma Kivrane, Agnija Namina, Agne Capligina, Valentina Poksane, Alise Ranka, Renate Oral microbiome variations related to ageing: possible implications beyond oral health |
title | Oral microbiome variations related to ageing: possible implications beyond oral health |
title_full | Oral microbiome variations related to ageing: possible implications beyond oral health |
title_fullStr | Oral microbiome variations related to ageing: possible implications beyond oral health |
title_full_unstemmed | Oral microbiome variations related to ageing: possible implications beyond oral health |
title_short | Oral microbiome variations related to ageing: possible implications beyond oral health |
title_sort | oral microbiome variations related to ageing: possible implications beyond oral health |
topic | Long Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10016173/ https://www.ncbi.nlm.nih.gov/pubmed/36920536 http://dx.doi.org/10.1007/s00203-023-03464-5 |
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