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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.
Affiliation
  • Chang HW; Department of Dermatology, University of California San Francisco, San Francisco, California, USA.
  • Yan D; Ronald O. Perelman Department of Dermatology, New York University Langone Health, New York, New York, USA.
  • Singh R; Department of Dermatology, Henry Ford Health System, Detroit, Michigan, USA.
  • Bui A; Department of Biology, St. Bonaventure University, St. Bonaventure, New York, USA.
  • Lee K; Department of Dermatology, University of California San Francisco, San Francisco, California, USA.
  • Truong A; Department of Nutritional Sciences & Toxicology, University of California Berkeley, Berkeley, California, USA.
  • Milush JM; Department of Medicine, University of California San Francisco, San Francisco, California, USA.
  • Somsouk M; Division of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, California, USA.
  • Liao W; Department of Dermatology, University of California San Francisco, San Francisco, California, USA.
JID Innov ; 2(3): 100115, 2022 May.
Article in En | MEDLINE | ID: mdl-35757783
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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: JID Innov Year: 2022 Document type: Article Affiliation country: United States Country of publication: Netherlands

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies / Risk_factors_studies Language: En Journal: JID Innov Year: 2022 Document type: Article Affiliation country: United States Country of publication: Netherlands