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Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese
Imbalance of the immune system caused by alterations of the gut microbiome is considered to be a critical factor in the pathogenesis of infant eczema, but the exact role of the gut microbiome in adult atopic dermatitis (AD) patients remains to be clarified. To investigate the differences of the gut...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454836/ https://www.ncbi.nlm.nih.gov/pubmed/37629036 http://dx.doi.org/10.3390/ijms241612856 |
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author | Wang, Yiwei Hou, Jinpao Tsui, Joseph Chi-Ching Wang, Lin Zhou, Junwei Chan, Un Kei Lo, Claudia Jun Yi Siu, Pui Ling Kella Loo, Steven King Fan Tsui, Stephen Kwok Wing |
author_facet | Wang, Yiwei Hou, Jinpao Tsui, Joseph Chi-Ching Wang, Lin Zhou, Junwei Chan, Un Kei Lo, Claudia Jun Yi Siu, Pui Ling Kella Loo, Steven King Fan Tsui, Stephen Kwok Wing |
author_sort | Wang, Yiwei |
collection | PubMed |
description | Imbalance of the immune system caused by alterations of the gut microbiome is considered to be a critical factor in the pathogenesis of infant eczema, but the exact role of the gut microbiome in adult atopic dermatitis (AD) patients remains to be clarified. To investigate the differences of the gut microbiome between adult AD patients and healthy individuals, stool samples of 234 adults, containing 104 AD patients and 130 healthy subjects, were collected for 16S rRNA gene amplicon. Altered structure and metabolic dysfunctions of the gut microbiome were identified in adult AD patients. Our results illustrated that the adult AD patients were more likely to have allergies, particularly non-food allergies. In addition, the gut microbiome composition of the AD and normal groups were considerably different. Moreover, Romboutsia and Clostridi-um_sensu_stricto_1 was enriched in the normal group, whereas Blautia, Butyricicoccus, Lachnoclostridium, Eubacterium_hallii_group, Erysi-pelatoclostridium, Megasphaera, Oscillibacter, and Flavonifractor dominated in the AD group. Additionally, purine nucleotide degradation pathways were significantly enriched in the AD group, and the enrichment of proteinogenic amino acid biosynthesis pathways was found in the normal group. This study provides insights into new therapeutic strategies targeting the gut microbiome for AD and evidence for the involvement of the gut–skin axis in AD patients. |
format | Online Article Text |
id | pubmed-10454836 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-104548362023-08-26 Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese Wang, Yiwei Hou, Jinpao Tsui, Joseph Chi-Ching Wang, Lin Zhou, Junwei Chan, Un Kei Lo, Claudia Jun Yi Siu, Pui Ling Kella Loo, Steven King Fan Tsui, Stephen Kwok Wing Int J Mol Sci Article Imbalance of the immune system caused by alterations of the gut microbiome is considered to be a critical factor in the pathogenesis of infant eczema, but the exact role of the gut microbiome in adult atopic dermatitis (AD) patients remains to be clarified. To investigate the differences of the gut microbiome between adult AD patients and healthy individuals, stool samples of 234 adults, containing 104 AD patients and 130 healthy subjects, were collected for 16S rRNA gene amplicon. Altered structure and metabolic dysfunctions of the gut microbiome were identified in adult AD patients. Our results illustrated that the adult AD patients were more likely to have allergies, particularly non-food allergies. In addition, the gut microbiome composition of the AD and normal groups were considerably different. Moreover, Romboutsia and Clostridi-um_sensu_stricto_1 was enriched in the normal group, whereas Blautia, Butyricicoccus, Lachnoclostridium, Eubacterium_hallii_group, Erysi-pelatoclostridium, Megasphaera, Oscillibacter, and Flavonifractor dominated in the AD group. Additionally, purine nucleotide degradation pathways were significantly enriched in the AD group, and the enrichment of proteinogenic amino acid biosynthesis pathways was found in the normal group. This study provides insights into new therapeutic strategies targeting the gut microbiome for AD and evidence for the involvement of the gut–skin axis in AD patients. MDPI 2023-08-16 /pmc/articles/PMC10454836/ /pubmed/37629036 http://dx.doi.org/10.3390/ijms241612856 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wang, Yiwei Hou, Jinpao Tsui, Joseph Chi-Ching Wang, Lin Zhou, Junwei Chan, Un Kei Lo, Claudia Jun Yi Siu, Pui Ling Kella Loo, Steven King Fan Tsui, Stephen Kwok Wing Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese |
title | Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese |
title_full | Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese |
title_fullStr | Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese |
title_full_unstemmed | Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese |
title_short | Unique Gut Microbiome Signatures among Adult Patients with Moderate to Severe Atopic Dermatitis in Southern Chinese |
title_sort | unique gut microbiome signatures among adult patients with moderate to severe atopic dermatitis in southern chinese |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10454836/ https://www.ncbi.nlm.nih.gov/pubmed/37629036 http://dx.doi.org/10.3390/ijms241612856 |
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