Austin Health

Title
Single nucleotide variations in ZBTB46 are associated with post-thrombolytic parenchymal haematoma.
Publication Date
2021-03-16
Author(s)
Carrera, Caty
Cárcel-Márquez, Jara
Cullell, Natalia
Torres-Águila, Nuria
Muiño, Elena
Castillo, José
Sobrino, Tomás
Campos, Francisco
Rodríguez-Castro, Emilio
Llucia-Carol, Laia
Millán, Mònica
Muñoz-Narbona, Lucía
López-Cancio, Elena
Bustamante, Alejandro
Ribó, Marc
Álvarez-Sabín, José
Jiménez-Conde, Jordi
Roquer, Jaume
Giralt-Steinhauer, Eva
Soriano-Tárraga, Carolina
Mola-Caminal, Marina
Vives-Bauza, Cristófol
Navarro, Rosa Díaz
Tur, Silvia
Obach, Victor
Arenillas, Juan Francisco
Segura, Tomás
Serrano-Heras, Gemma
Martí-Fàbregas, Joan
Delgado-Mederos, Raquel
Freijo-Guerrero, M Mar
Moniche, Francisco
Cabezas, Juan Antonio
Castellanos, Mar
Gallego-Fabrega, Cristina
González-Sanchez, Jonathan
Krupinsky, Jurek
Strbian, Daniel
Tatlisumak, Turgut
Thijs, Vincent
Lemmens, Robin
Slowik, Agnieszka
Pera, Johanna
Kittner, Steven
Cole, John
Heitsch, Laura
Ibañez, Laura
Cruchaga, Carlos
Lee, Jin-Moo
Montaner, Joan
Fernández-Cadenas, Israel
Subject
GWAs
ischemic Stroke
parenchymal hematoma
pharmacogenetics
thrombolysis
Type of document
Journal Article
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DOI
10.1093/brain/awab090
Abstract
Hemorrhagic transformation is a complication of recombinant tissue-plasminogen activator (rtPA) treatment. The most severe form, parenchymal hematoma, can result in neurological deterioration, disability, and death. Our objective is to identify single nucleotide variations associated with a risk of parenchymal hematoma following thrombolytic therapy in acute ischemic stroke patients. A fixed-effect genome-wide metanalysis was performed combining two-stage Genome Wide Association studies (GWAs) (n = 1,904). The Discovery Stage (3 cohorts) comprised 1,324 ischemic stroke individuals, of whom 5.4% had a parenchymal hematoma. Genetic variants yielding a p-value <1x10-5 were analyzed in the Validation Stage (6 cohorts), formed by 580 ischemic stroke patients with 12.1% hemorrhagic events. All the participants received rtPA; cases were parenchymal hematoma type 1 or 2 as defined by the ECASS criteria. Genome-wide significant findings (p < 5x10-8) were characterized by in-silico functional annotation, gene expression, and DNA regulatory elements. We analyzed 7,989,272 single nucleotide polymorphisms (SNPs) and identified a Genome-wide association locus on chromosome 20 in the Discovery Cohort; functional annotation indicated that the ZBTB46 gene was driving the association for Chrosome 20. The top SNP was rs76484331 in the ZBTB46 gene (p = 2.49x10-8; odds ratio (OR): 11.21; 95% confidence interval (CI): 4.82-26.55). In the Replication Cohort (n = 580), the rs76484331 polymorphism was associated with parenchymal hematoma (p = 0.01), and the overall association after meta-analysis increased (p = 1.61x10-8; OR: 5.84; 95%CI: 3.16-10.76). ZBTB46 codes the Zinc Finger and BTB domain-containing protein 46 that acts as a transcription factor. In-silico studies indicated that ZBTB46 is expressed in brain tissue by neurons and endothelial cells. Moreover, rs76484331 interacts with the promoter sites located at 20q13. In conculsion, we identified single nucleotide variants in the ZBTB46 gene associated with a higher risk of parenchymal hematoma following rtPA treatment.
Link
Citation
Brain 2021; online first: 16 March
Jornal Title
Brain

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