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Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations
Psoriasis is a chronic, inflammatory skin disease that affects 2‒3% of the global population. Besides skin manifestations, patients with psoriasis have increased susceptibility to a number of comorbidities, including psoriatic arthritis, cardiovascular disease, and inflammatory bowel disease. To und...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214347/ https://www.ncbi.nlm.nih.gov/pubmed/35757783 http://dx.doi.org/10.1016/j.xjidi.2022.100115 |
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author | Chang, Hsin-Wen Yan, Di Singh, Rasnik Bui, Audrey Lee, Kristina Truong, Alexa Milush, Jeffrey M. Somsouk, Ma Liao, Wilson |
author_facet | Chang, Hsin-Wen Yan, Di Singh, Rasnik Bui, Audrey Lee, Kristina Truong, Alexa Milush, Jeffrey M. Somsouk, Ma Liao, Wilson |
author_sort | Chang, Hsin-Wen |
collection | PubMed |
description | Psoriasis is a chronic, inflammatory skin disease that affects 2‒3% of the global population. Besides skin manifestations, patients with psoriasis have increased susceptibility to a number of comorbidities, including psoriatic arthritis, cardiovascular disease, and inflammatory bowel disease. To understand the systemic component of psoriasis pathogenesis, we performed a pilot study to examine the fecal metagenome, host colonic transcriptome, and host peripheral blood immune profiles of patients with psoriasis and healthy controls. Our study showed increased functional diversity in the gut microbiome of patients with psoriasis. In addition, we identified microbial species that preferentially associate with patients with psoriasis and which have been previously found to associate with other autoimmune diseases. Intriguingly, our data revealed three psoriasis subgroups that have distinct microbial and host features. Integrating these features revealed host‒microbe associations that are specific to psoriasis or particular psoriasis subgroups. Our findings provide insight into the factors that may affect the development of comorbidities in patients with psoriasis and may hold diagnostic potential for early identification of patients with psoriasis at risk for these comorbidities. |
format | Online Article Text |
id | pubmed-9214347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92143472022-06-23 Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations Chang, Hsin-Wen Yan, Di Singh, Rasnik Bui, Audrey Lee, Kristina Truong, Alexa Milush, Jeffrey M. Somsouk, Ma Liao, Wilson JID Innov Original Article Psoriasis is a chronic, inflammatory skin disease that affects 2‒3% of the global population. Besides skin manifestations, patients with psoriasis have increased susceptibility to a number of comorbidities, including psoriatic arthritis, cardiovascular disease, and inflammatory bowel disease. To understand the systemic component of psoriasis pathogenesis, we performed a pilot study to examine the fecal metagenome, host colonic transcriptome, and host peripheral blood immune profiles of patients with psoriasis and healthy controls. Our study showed increased functional diversity in the gut microbiome of patients with psoriasis. In addition, we identified microbial species that preferentially associate with patients with psoriasis and which have been previously found to associate with other autoimmune diseases. Intriguingly, our data revealed three psoriasis subgroups that have distinct microbial and host features. Integrating these features revealed host‒microbe associations that are specific to psoriasis or particular psoriasis subgroups. Our findings provide insight into the factors that may affect the development of comorbidities in patients with psoriasis and may hold diagnostic potential for early identification of patients with psoriasis at risk for these comorbidities. Elsevier 2022-03-10 /pmc/articles/PMC9214347/ /pubmed/35757783 http://dx.doi.org/10.1016/j.xjidi.2022.100115 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Chang, Hsin-Wen Yan, Di Singh, Rasnik Bui, Audrey Lee, Kristina Truong, Alexa Milush, Jeffrey M. Somsouk, Ma Liao, Wilson Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations |
title | Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations |
title_full | Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations |
title_fullStr | Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations |
title_full_unstemmed | Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations |
title_short | Multiomic Analysis of the Gut Microbiome in Psoriasis Reveals Distinct Host‒Microbe Associations |
title_sort | multiomic analysis of the gut microbiome in psoriasis reveals distinct host‒microbe associations |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214347/ https://www.ncbi.nlm.nih.gov/pubmed/35757783 http://dx.doi.org/10.1016/j.xjidi.2022.100115 |
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