The clinical utility of functional testing in fibroblasts to diagnose primary mitochondrial disease
Van Hove, J. L. K.; Friederich, M. W.; Van Hove, R. A.; Lee, J. C.; Knight, K. M.; Donovan, T. E.; Silveira, L.; Ganetzky, R.; Hirano, M.; Abdenur, J. E.; Butler, M. G.; Cassiman, D.; Cohen, B. H.; Elsea, S. H.; Enns, G. M.; Gahl, W. A.; Gavrilova, R.; Geddes, G. C.; Glamuzima, E. E.; Goldstein, A. C.; Haas, R. H.; Khan, A.; Kripps, K. A.; Larson, A.; Lehman, A. N.; Lichter-Konecki, U.; Mayr, J. A.; Morava, E.; Peterson, J. T.; Rosenfeld, J. A.; Saneto, R. P.; Scaglia, F.; Shelkowitz, E.; Simon, M. T.; Smet, J. E.; Smith, W. E.; Soler-Alfonso, C.; Tarnopolsky, M. A.; Van Coster, R. N. A.; Vanl
Show abstract
Genome sequencing of the heterogeneous primary mitochondrial disorders (PMD) frequently reveals variants of uncertain significance that require functional tests for diagnosis, and does not identify variants in all patients. We analyzed mitochondrial enzyme assays, blue native polyacrylamide gel electrophoresis (BN-PAGE) with in-gel activity staining, complex I assembly blot, and select protein abundances in fibroblasts of a case series of 204 PMD patients divided into functional classes, in comparison to 51 controls and 53 differential diagnostic conditions. Overall, sensitivity and specificity for respiratory chain enzyme assays were 46% and 93% respectively, for BN-PAGE 40% and 98%, for complex I assembly assay 49% and 99%. The overall sensitivity of all tests was 76%, specificity 93%, with positive predictive value 96% and negative predictive value 67%. Categories with high sensitivity were isolated complex deficiencies, nuclear DNA-encoded mitochondrial protein synthesis defects, co-factor defects, and mitochondrial amino-acyl-tRNA synthetase conditions when aided by protein abundance. Mitochondrial DNA mutations and maintenance disorders showed poor sensitivities. Secondary dysfunctions were rare. A complete battery of functional tests showed strong diagnostic clinical utility in fibroblasts.
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