4.7 Article

Altered Skin and Gut Microbiome in Hidradenitis Suppurativa

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JOURNAL OF INVESTIGATIVE DERMATOLOGY
卷 142, 期 2, 页码 459-+

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.jid.2021.05.036

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  1. City of Dublin Skin Cancer Hospital Charity (Dublin, Ireland)
  2. Irish Centre for Arthritis Research and Education (Cork, Ireland)
  3. Science Foundation Ireland through a Centre award [APC/SFI/12/RC/2273_P2]

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Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease characterized by nodules, abscesses, and fistulae. This study found that individuals with HS had lower microbial diversity in fecal, skin, and nasal samples, and certain bacteria were more abundant. Finegoldia magna was overabundant in HS skin samples, potentially contributing to local inflammation. These findings suggest that the microbiome alterations in both the gut and skin of HS patients deserve further investigation.
Hidradenitis suppurativa (HS) is a chronic inflammatory skin disease characterized by the formation of nodules, abscesses, and fistulae at intertriginous sites. The skinegut axis is an area of emerging research in inflammatory skin disease and is a potential contributory factor to the pathogenesis of HS. A total of 59 patients with HS provided fecal samples and nasal and skin swabs of affected sites for analysis. A total of 30 healthy controls provided fecal samples, and 20 healthy controls provided nasal and skin swabs. We performed bacterial 16S ribosomal RNA gene amplicon sequencing on total DNA derived from the samples. Microbiome alpha diversity was significantly lower in the fecal, skin, and nasal samples of individuals with HS, which may be secondary to disease biology or related to antibiotic usage. Ruminococcus gnavus was more abundant in the fecal microbiome of individuals with HS, which is also reported in Crohn's disease, suggesting comorbidity due to shared gut microbiota alterations. Finegoldia magna was overabundant in HS skin samples relative to that in the healthy controls. It is possible that local inflammation is driven by F. magna by promoting the formation of neutrophil extracellular traps. These alterations in both the gut and skin microbiome in HS warrant further exploration, and therapeutic strategies, including fecal microbiota transplant or bacteriotherapy, could be of benefit.

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