<abstract xmlns="http://www.w3.org/1999/xhtml">

<p>The knowledge of causes and pathophysiology of mitochondrial diseases has increased exponentially in the last four decades. Recently, due to the decreased costs of new sequencing technologies (exome and whole genome sequencing), these technologies were applied more and more in clinical routine. The traditional diagnostic approach (‘biopsy first’) of evaluating the patient and his body fluids and the analysis of enzymes of the oxidative phosphorylation system in skeletal muscle with subsequent Sanger sequencing of single candidate genes (‘from function to gene’) were replaced by next generation sequencing techniques with a diagnostic yield of >40%. In this ‘genetics first’ approach, the detection of new candidate genes necessitates often functional evaluations (‘from gene to function’) leading to reverse phenotyping of affected individuals. The new genetic era has offered a clear new challenge for the responsibility of the diagnostic centres: the interplay of clinicians, geneticists and functional biochemists is a prerequisite for a validated diagnosis. It becomes evident that expanded diagnostics builds an interface to research. Only competence centres with high numbers of patients, clinical and diagnostic experience and exchange of knowledge with other comparable units can fulfil all those requirements.</p></abstract>

The knowledge of causes and pathophysiology of mitochondrial diseases has increased exponentially in the last four decades. Recently, due to the decreased costs of new sequencing technologies (exome and whole genome sequencing), these technologies were applied more and more in clinical routine. The traditional diagnostic approach (‘biopsy first’) of evaluating the patient and his body fluids and the analysis of enzymes of the oxidative phosphorylation system in skeletal muscle with subsequent Sanger sequencing of single candidate genes (‘from function to gene’) were replaced by next generation sequencing techniques with a diagnostic yield of >40%. In this ‘genetics first’ approach, the detection of new candidate genes necessitates often functional evaluations (‘from gene to function’) leading to reverse phenotyping of affected individuals. The new genetic era has offered a clear new challenge for the responsibility of the diagnostic centres: the interplay of clinicians, geneticists and functional biochemists is a prerequisite for a validated diagnosis. It becomes evident that expanded diagnostics builds an interface to research. Only competence centres with high numbers of patients, clinical and diagnostic experience and exchange of knowledge with other comparable units can fulfil all those requirements.

The switch in the diagnosis of mitochondrial diseases from the classical ‘function first’ to the NGS-based ‘genetics first’ diagnostic era

Journal of Mother and Child

This work is licensed under the Creative Commons Attribution 4.0 International License.

The knowledge of causes and pathophysiology of mitochondrial diseases has increased exponentially in the last four decades. Recently, due to the decreased...

The switch in the diagnosis of mitochondrial diseases from the classical ‘function first’ to the NGS-based ‘genetics first’ diagnostic era

Article Category: Review paper

Online veröffentlicht: 02. Okt. 2020

Seitenbereich: 47 - 52

DOI: https://doi.org/10.34763/jmotherandchild.20202402si.2005.000008

Schlüsselwörter
mitochondrial diseases, OXPHOS, paediatrics, diagnostics, next generation sequencing, exome sequencing, whole genome sequencing, mitochondrial DNA, diagnostic centres

© 2020 Wolfgang Sperl et al. published by Sciendo

This work is licensed under the Creative Commons Attribution 4.0 International License.

The switch in the diagnosis of mitochondrial diseases from the classical ‘function first’ to the NGS-based ‘genetics first’ diagnostic era

Article Category: Review paper

Online veröffentlicht: 02. Okt. 2020

Seitenbereich: 47 - 52

DOI: https://doi.org/10.34763/jmotherandchild.20202402si.2005.000008

Schlüsselwörtermitochondrial diseases, OXPHOS, paediatrics, diagnostics, next generation sequencing, exome sequencing, whole genome sequencing, mitochondrial DNA, diagnostic centres

© 2020 Wolfgang Sperl et al. published by Sciendo

This work is licensed under the Creative Commons Attribution 4.0 International License.

Schlüsselwörter
mitochondrial diseases, OXPHOS, paediatrics, diagnostics, next generation sequencing, exome sequencing, whole genome sequencing, mitochondrial DNA, diagnostic centres