Hidradenitis Suppurativa and 1-Carbon Metabolism: Role of Gut Microbiome, Matrix Metalloproteinases, and Hyperhomocysteinemia

Front Immunol. 2020 Aug 19:11:1730. doi: 10.3389/fimmu.2020.01730. eCollection 2020.

Abstract

Hidradenitis suppurativa (HS) is a chronic, inflammatory skin condition characterized by painful nodules which suppurate and later develop into scar tissues followed by the development of hypodermal tracts. Although the mechanisms behind HS are not fully understood, it is known that dietary factors play important roles in flare frequency and severity. We hypothesize that the high fat diet (HFD) causes dysbiosis, systemic inflammation, and hyperhomocysteinemia (HHcy) in susceptible individuals, which subsequently elevate inflammatory cytokines such as IL-1β, IL-6, IL-17, and tumor necrosis factor alpha (TNF-α). This increase in dysbiosis-led inflammation coupled with a dysregulation of the 1-carbon metabolism results in an increase in matrix metalloproteinases MMP-2, MMP-8, and MMP-9 along with tissue matrix remodeling in the development and maintenance of the lesions and tracts. This manuscript weaves together the potential roles played by the gut microbiome, HHcy, MMPs, and the 1-carbon metabolism toward HS disease causation in susceptible individuals.

Keywords: acne; dysbiosis; extracellular matrix; homocysteine; tissue remodeling.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Bacteria / metabolism*
  • Biomarkers / blood
  • Diet, High-Fat / adverse effects*
  • Dysbiosis
  • Gastrointestinal Microbiome*
  • Hidradenitis Suppurativa / enzymology
  • Hidradenitis Suppurativa / etiology*
  • Hidradenitis Suppurativa / microbiology
  • Hidradenitis Suppurativa / pathology
  • Homocysteine / blood*
  • Humans
  • Hyperhomocysteinemia / blood
  • Hyperhomocysteinemia / complications*
  • Matrix Metalloproteinases / metabolism*
  • Risk Assessment
  • Risk Factors
  • Skin / enzymology*
  • Skin / pathology

Substances

  • Biomarkers
  • Homocysteine
  • Matrix Metalloproteinases