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Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients

Gout is a prevalent chronic inflammatory disease that affects the life of tens of millions of people worldwide, and it typically presents as gout arthritis, gout stone, or even kidney damage. Research has revealed its connection with the gut microbiome, although exact mechanism is still unclear. Stu...

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Autores principales: Zhou, Jieshang, Yuan, Yali, Xu, Pengli, Yi, Bin, Chen, Hongju, Su, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109170/
https://www.ncbi.nlm.nih.gov/pubmed/35586773
http://dx.doi.org/10.1177/11769343221095858
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author Zhou, Jieshang
Yuan, Yali
Xu, Pengli
Yi, Bin
Chen, Hongju
Su, Wei
author_facet Zhou, Jieshang
Yuan, Yali
Xu, Pengli
Yi, Bin
Chen, Hongju
Su, Wei
author_sort Zhou, Jieshang
collection PubMed
description Gout is a prevalent chronic inflammatory disease that affects the life of tens of millions of people worldwide, and it typically presents as gout arthritis, gout stone, or even kidney damage. Research has revealed its connection with the gut microbiome, although exact mechanism is still unclear. Studies have shown the decline of microbiome diversity in gout patients and change of microbiome compositions between the gout patients and healthy controls. Nevertheless, how diversity changes across host individuals at a cohort (population) level has not been investigated to the best of our knowledge. Here we apply the diversity-area relationship (DAR), which is an extension to the classic SAR (species-area relationship) and establishes the power-function model between microbiome diversity and the number of individuals within cohort, to comparatively investigate diversity scaling (changes) of gut microbiome in gout patients and healthy controls. The DAR modeling with a study involving 83 subjects (41 gout patients) revealed that the potential number of microbial species in gout patients is only 70% of that in the healthy control (2790 vs 3900) although the difference may not be statistically significant. The other DAR parameters including diversity scaling and similarity parameters did not show statistically significant differences. We postulate that the high resilience of gut microbiome may explain the lack of significant gout-disease effects on gut microbial diversity at the population level. The lack of statistically significant difference between the gout patients and healthy controls at host population (cohort) level is different from the previous findings at individual level in the existing literature.
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spelling pubmed-91091702022-05-17 Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients Zhou, Jieshang Yuan, Yali Xu, Pengli Yi, Bin Chen, Hongju Su, Wei Evol Bioinform Online Metagenomics and the analysis of microbiomes Gout is a prevalent chronic inflammatory disease that affects the life of tens of millions of people worldwide, and it typically presents as gout arthritis, gout stone, or even kidney damage. Research has revealed its connection with the gut microbiome, although exact mechanism is still unclear. Studies have shown the decline of microbiome diversity in gout patients and change of microbiome compositions between the gout patients and healthy controls. Nevertheless, how diversity changes across host individuals at a cohort (population) level has not been investigated to the best of our knowledge. Here we apply the diversity-area relationship (DAR), which is an extension to the classic SAR (species-area relationship) and establishes the power-function model between microbiome diversity and the number of individuals within cohort, to comparatively investigate diversity scaling (changes) of gut microbiome in gout patients and healthy controls. The DAR modeling with a study involving 83 subjects (41 gout patients) revealed that the potential number of microbial species in gout patients is only 70% of that in the healthy control (2790 vs 3900) although the difference may not be statistically significant. The other DAR parameters including diversity scaling and similarity parameters did not show statistically significant differences. We postulate that the high resilience of gut microbiome may explain the lack of significant gout-disease effects on gut microbial diversity at the population level. The lack of statistically significant difference between the gout patients and healthy controls at host population (cohort) level is different from the previous findings at individual level in the existing literature. SAGE Publications 2022-05-13 /pmc/articles/PMC9109170/ /pubmed/35586773 http://dx.doi.org/10.1177/11769343221095858 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Metagenomics and the analysis of microbiomes
Zhou, Jieshang
Yuan, Yali
Xu, Pengli
Yi, Bin
Chen, Hongju
Su, Wei
Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients
title Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients
title_full Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients
title_fullStr Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients
title_full_unstemmed Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients
title_short Host-Population Microbial Diversity Scaling of Chinese Gut Microbiomes in Gout Patients
title_sort host-population microbial diversity scaling of chinese gut microbiomes in gout patients
topic Metagenomics and the analysis of microbiomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109170/
https://www.ncbi.nlm.nih.gov/pubmed/35586773
http://dx.doi.org/10.1177/11769343221095858
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