AI Article Synopsis

  • Mitochondrial disease (MD) is difficult to diagnose, often requiring invasive procedures like muscle biopsies, but blood cell respirometry offers a quick and noninvasive alternative.
  • A study involving 113 pediatric patients found that a specific respiratory analysis could identify MD with 96% specificity, though no individual measure had high sensitivity; however, a combined approach achieved 72% sensitivity.
  • While normal platelet respirometry results don't rule out MD, abnormal findings can increase the likelihood of the disease and support further invasive testing, indicating the need for additional research into this diagnostic method.

Article Abstract

BackgroundDiagnosing mitochondrial disease (MD) is a challenge. In addition to genetic analyses, clinical practice is to perform invasive procedures such as muscle biopsy for biochemical and histochemical analyses. Blood cell respirometry is rapid and noninvasive. Our aim was to explore its possible role in diagnosing MD.MethodsBlood samples were collected from 113 pediatric patients, for whom MD was a differential diagnosis. A respiratory analysis model based on ratios (independent of mitochondrial specific content) was derived from a group of healthy controls and tested on the patients. The diagnostic accuracy of platelet respirometry was evaluated against routine diagnostic investigation.ResultsMD prevalence in the cohort was 16%. A ratio based on the respiratory response to adenosine diphosphate in the presence of complex I substrates had 96% specificity for disease and a positive likelihood ratio of 5.3. None of the individual ratios had sensitivity above 50%, but a combined model had 72% sensitivity.ConclusionNormal findings of platelet respirometry are not able to rule out MD, but pathological results make the diagnosis more likely and could strengthen the clinical decision to perform further invasive analyses. Our results encourage further study into the role of blood respirometry as an adjunct diagnostic tool for MD.

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Source
http://dx.doi.org/10.1038/pr.2017.250DOI Listing

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