Molecular EPISTOP, a comprehensive multi-omic analysis of blood from Tuberous Sclerosis Complex infants age birth to two years
Huschner, Franz; Głowacka-Walas, Jagoda; Mills, James D; Klonowska, Katarzyna; Lasseter, Kathryn; Asara, John M; Moavero, Romina; Hertzberg, Christoph; Weschke, Bernhard; Riney, Kate; Feucht, Martha; Scholl, Theresa; Krsek, Pavel; Nabbout, Rima; Jansen, Anna C; Petrák, Bořivoj; van Scheppingen, Jackelien; Zamecnik, Josef; Iyer, Anand; Anink, Jasper J; Mühlebner, Angelika; Mijnsbergen, Caroline; Lagae, Lieven; Curatolo, Paolo; Borkowska, Julita; Sadowski, Krzysztof; Domańska-Pakieła, Dorota; Blazejczyk, Magdalena; Jansen, Floor E; Janson, Stef; Urbanska, Malgorzata; Tempes, Aleksandra; Janssen, Bart; Sijko, Kamil; Wojdan, Konrad; Jozwiak, Sergiusz; Kotulska, Katarzyna; Lehmann, Karola; Aronica, Eleonora; Jaworski, Jacek; Kwiatkowski, David J
(2023) Nature Communications, volume 14, issue 1
(Article)
Abstract
We present a comprehensive multi-omic analysis of the EPISTOP prospective clinical trial of early intervention with vigabatrin for pre-symptomatic epilepsy treatment in Tuberous Sclerosis Complex (TSC), in which 93 infants with TSC were followed from birth to age 2 years, seeking biomarkers of epilepsy development. Vigabatrin had profound effects on
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many metabolites, increasing serum deoxycytidine monophosphate (dCMP) levels 52-fold. Most serum proteins and metabolites, and blood RNA species showed significant change with age. Thirty-nine proteins, metabolites, and genes showed significant differences between age-matched control and TSC infants. Six also showed a progressive difference in expression between control, TSC without epilepsy, and TSC with epilepsy groups. A multivariate approach using enrollment samples identified multiple 3-variable predictors of epilepsy, with the best having a positive predictive value of 0.987. This rich dataset will enable further discovery and analysis of developmental effects, and associations with seizure development in TSC.
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Keywords: Journal Article
ISSN: 2041-1723
Publisher: Nature Publishing Group
Note: Publisher Copyright: © 2023, The Author(s).
(Peer reviewed)