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Emerging concepts in the therapy of mitochondrial disease

Biochim Biophys Acta. 2015 Jun-Jul;1847(6-7):544-57. doi: 10.1016/j.bbabio.2015.03.001. Epub 2015 Mar 10.

Abstract

Mitochondrial disorders are an important group of genetic conditions characterized by impaired oxidative phosphorylation. Mitochondrial disorders come with an impressive variability of symptoms, organ involvement, and clinical course, which considerably impact the quality of life and quite often shorten the lifespan expectancy. Although the last 20 years have witnessed an exponential increase in understanding the genetic and biochemical mechanisms leading to disease, this has not resulted in the development of effective therapeutic approaches, amenable of improving clinical course and outcome of these conditions to any significant extent. Therapeutic options for mitochondrial diseases still remain focused on supportive interventions aimed at relieving complications. However, new therapeutic strategies have recently been emerging, some of which have shown potential efficacy at the pre-clinical level. This review will present the state of the art on experimental therapy for mitochondrial disorders.

Keywords: Animal model; Experimental therapy; Mitochondrial disease; Mitochondrial respiratory chain; Mitochondrion; Oxidative phosphorilation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Electron Transport
  • Humans
  • Mitochondrial Diseases / metabolism
  • Mitochondrial Diseases / pathology
  • Mitochondrial Diseases / therapy*
  • Oxidative Phosphorylation