Mitochondrial DNA mutations in renal disease: an overview.

Larissa P Govers, Hakan R Toka, Ali Hariri, Stephen B Walsh, Detlef Bockenhauer

Journal: Pediatric nephrology (Berlin, Germany) 2021;36(1):9-17

PMID: 31925537

Abstract

Kidneys have a high energy demand to facilitate the reabsorption of the glomerular filtrate. For this reason, renal cells have a high density of mitochondria. Mitochondrial cytopathies can be the result of a mutation in both mitochondrial and nuclear DNA. Mitochondrial dysfunction can lead to a variety of renal manifestations. Examples of tubular manifestations are renal Fanconi Syndrome, which is often found in patients diagnosed with Kearns-Sayre and Pearson's marrow-pancreas syndrome, and distal tubulopathies, which result in electrolyte disturbances such as hypomagnesemia. Nephrotic syndrome can be a glomerular manifestation of mitochondrial dysfunction and is typically associated with focal segmental glomerular sclerosis on histology. Tubulointerstitial nephritis can also be seen in mitochondrial cytopathies and may lead to end-stage renal disease. The underlying mechanisms of these cytopathies remain incompletely understood; therefore, current therapies focus mainly on symptom relief. A better understanding of the molecular disease mechanisms is critical in order to improve treatments.

Address: Department of Renal Medicine, University College London, London, UK.; Manatee Kidney Diseases Consultants, Bradenton, USA.; Clinical Development, Sanofi Rare Disease, Boston, USA.; Department of Renal Medicine, University College London, London, UK. [email protected].; Renal Unit, Great Ormond Street Hospital for Children NHS Foundation Trust, Great Ormond Street, London, UK. [email protected].
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