Systemic sclerosis-associated fibrosis: an accelerated aging phenotype?

Curr Opin Rheumatol. 2015 Nov;27(6):571-6. doi: 10.1097/BOR.0000000000000219.

Abstract

Purpose of review: Systemic sclerosis (SSc) is an autoimmune disease with fibrosis seen in multiple organs. Although not traditionally regarded as a disease of aging, SSc-associated fibrosis shares many of the hallmarks of aging seen in other age-related fibrotic disorders. Here, we review the current literature of the potential role of aging and age-related cellular processes in the development of SSc and fibrosis.

Recent findings: Accumulating evidence supports a role for immune dysregulation, epigenetic modifications, cellular senescence, mitochondrial dysregulation and impaired autophagy in fibrosis that occurs in aging and SSc.

Summary: Cellular alterations linked to aging may promote the development and/or progression of SSc-associated fibrosis.

Publication types

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

MeSH terms

  • Aging / genetics
  • Aging / immunology
  • Aging / physiology*
  • Autophagy / physiology
  • Cellular Senescence / genetics
  • Cellular Senescence / immunology
  • Cellular Senescence / physiology
  • Epigenesis, Genetic
  • Fibroblasts / immunology
  • Fibroblasts / pathology
  • Fibroblasts / physiology
  • Fibrosis
  • Humans
  • Mitochondrial Diseases / immunology
  • Mitochondrial Diseases / physiopathology
  • Phenotype
  • Scleroderma, Systemic / immunology
  • Scleroderma, Systemic / pathology
  • Scleroderma, Systemic / physiopathology*