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MERRF Classification: Implications for Diagnosis and Clinical Trials.

Authors
  • Finsterer, Josef1
  • Zarrouk-Mahjoub, Sinda2
  • Shoffner, John M3
  • 1 Krankenanstalt Rudolfstiftung, Vienna, Austria. Electronic address: [email protected]. , (Austria)
  • 2 University of Tunis El Manar and Genomics Platform, Pasteur Institute of Tunis, Tunisia. , (Tunisia)
  • 3 Neurology, Biochemical Genetics, Molecular Genetics, Atlanta, Georgia. , (Georgia)
Type
Published Article
Journal
Pediatric neurology
Publication Date
Mar 01, 2018
Volume
80
Pages
8–23
Identifiers
DOI: 10.1016/j.pediatrneurol.2017.12.005
PMID: 29449072
Source
Medline
Keywords
Language
English
License
Unknown

Abstract

Given the etiologic heterogeneity of disease classification using clinical phenomenology, we employed contemporary criteria to classify variants associated with myoclonic epilepsy with ragged-red fibers (MERRF) syndrome and to assess the strength of evidence of gene-disease associations. Standardized approaches are used to clarify the definition of MERRF, which is essential for patient diagnosis, patient classification, and clinical trial design. Systematic literature and database search with application of standardized assessment of gene-disease relationships using modified Smith criteria and of variants reported to be associated with MERRF using modified Yarham criteria. Review of available evidence supports a gene-disease association for two MT-tRNAs and for POLG. Using modified Smith criteria, definitive evidence of a MERRF gene-disease association is identified for MT-TK. Strong gene-disease evidence is present for MT-TL1 and POLG. Functional assays that directly associate variants with oxidative phosphorylation impairment were critical to mtDNA variant classification. In silico analysis was of limited utility to the assessment of individual MT-tRNA variants. With the use of contemporary classification criteria, several mtDNA variants previously reported as pathogenic or possibly pathogenic are reclassified as neutral variants. MERRF is primarily an MT-TK disease, with pathogenic variants in this gene accounting for ~90% of MERRF patients. Although MERRF is phenotypically and genotypically heterogeneous, myoclonic epilepsy is the clinical feature that distinguishes MERRF from other categories of mitochondrial disorders. Given its low frequency in mitochondrial disorders, myoclonic epilepsy is not explained simply by an impairment of cellular energetics. Although MERRF phenocopies can occur in other genes, additional data are needed to establish a MERRF disease-gene association. This approach to MERRF emphasizes standardized classification rather than clinical phenomenology, thus improving patient diagnosis and clinical trial design. Copyright © 2017 Elsevier Inc. All rights reserved.

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