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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...

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Autores principales: Chang, Hsin-Wen, Yan, Di, Singh, Rasnik, Bui, Audrey, Lee, Kristina, Truong, Alexa, Milush, Jeffrey M., Somsouk, Ma, Liao, Wilson
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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.
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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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