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Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset
N. Mirza-Schreiber, M. Zech, R. Wilson, T. Brunet, M. Wagner, R. Jech, S. Boesch, M. Škorvánek, J. Necpál, D. Weise, S. Weber, B. Mollenhauer, C. Trenkwalder, EM. Maier, I. Borggraefe, K. Vill, A. Hackenberg, V. Pilshofer, U. Kotzaeridou, EMC....
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 1996 do Před 1 rokem
Open Access Digital Library
od 1996-01-01
PubMed
34590685
DOI
10.1093/brain/awab360
Knihovny.cz E-zdroje
- MeSH
- biologické markery MeSH
- dystonické poruchy * genetika terapie MeSH
- dystonie * genetika terapie MeSH
- histonlysin-N-methyltransferasa genetika MeSH
- lidé MeSH
- metylace DNA genetika MeSH
- mutace MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Dystonia is a prevalent, heterogeneous movement disorder characterized by involuntarily abnormal postures. Biomarkers of dystonia are notoriously lacking. Here, a biomarker is reported for histone lysine methyltransferase (KMT2B)-deficient dystonia, a leading subtype among the individually rare monogenic dystonias. It was derived by applying a support vector machine to an episignature of 113 DNA CpG sites, which, in blood cells, showed significant epigenome-wide association with KMT2B deficiency and at least 1× log-fold change of methylation. This classifier was accurate both when tested on the general population and on samples with various other deficiencies of the epigenetic machinery, thus allowing for definitive evaluation of variants of uncertain significance and identifying patients who may profit from deep brain stimulation, a highly successful treatment in KMT2B-deficient dystonia. Methylation was increased in KMT2B deficiency at all 113 CpG sites. The coefficients of variation of the normalized methylation levels at these sites also perfectly classified the samples with KMT2B-deficient dystonia. Moreover, the mean of the normalized methylation levels correlated well with the age at onset of dystonia (P = 0.003)-being lower in samples with late or incomplete penetrance-thus serving as a predictor of disease onset and severity. Similarly, it may also function in monitoring the recently envisioned treatment of KMT2B deficiency by inhibition of DNA methylation.
Chair of Neurogenetics Technical University of Munich School of Medicine 81675 Munich Germany
Department of Neurology Asklepios Fachklinikum Stadtroda 07646 Stadtroda Germany
Department of Neurology Medizinische Universität 6020 Insbruck Austria
Department of Neurology P J Safarik University 04011 Kosice Slovakia
Department of Neurology University Hospital L Pasteur 04011 Kosice Slovakia
Department of Neurology University of Leipzig 04103 Leipzig Germany
Department of Neurology Zvolen Hospital 96001 Zvolen Slovakia
Department of Pediatric Neurology University Children's Hospital 8032 Zürich Switzerland
Dr von Hauner Children's Hospital Ludwig Maximilians University 80337 Munich Germany
German Center for Diabetes Research 85764 Neuherberg Germany
Institute of Human Genetics Heidelberg University 69120 Heidelberg Germany
Institute of Human Genetics Technical University of Munich School of Medicine 81675 Munich Germany
Munich Cluster for Systems Neurology 81377 Munich Germany
Ordensklinikum Linz Barmherzige Schwestern 4010 Linz Austria
Citace poskytuje Crossref.org
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