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NOTCH3 Variants and Risk of Ischemic Stroke

BACKGROUND: Mutations within the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). CADASIL mutations appear to be restricted to the first twenty-four exons, resulting in the gain or loss of a cysteine amino acid. The role of other...

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Autores principales: Ross, Owen A., Soto-Ortolaza, Alexandra I., Heckman, Michael G., Verbeeck, Christophe, Serie, Daniel J., Rayaprolu, Sruti, Rich, Stephen S., Nalls, Michael A., Singleton, Andrew, Guerreiro, Rita, Kinsella, Emma, Wszolek, Zbigniew K., Brott, Thomas G., Brown, Robert D., Worrall, Bradford B., Meschia, James F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781028/
https://www.ncbi.nlm.nih.gov/pubmed/24086431
http://dx.doi.org/10.1371/journal.pone.0075035
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author Ross, Owen A.
Soto-Ortolaza, Alexandra I.
Heckman, Michael G.
Verbeeck, Christophe
Serie, Daniel J.
Rayaprolu, Sruti
Rich, Stephen S.
Nalls, Michael A.
Singleton, Andrew
Guerreiro, Rita
Kinsella, Emma
Wszolek, Zbigniew K.
Brott, Thomas G.
Brown, Robert D.
Worrall, Bradford B.
Meschia, James F.
author_facet Ross, Owen A.
Soto-Ortolaza, Alexandra I.
Heckman, Michael G.
Verbeeck, Christophe
Serie, Daniel J.
Rayaprolu, Sruti
Rich, Stephen S.
Nalls, Michael A.
Singleton, Andrew
Guerreiro, Rita
Kinsella, Emma
Wszolek, Zbigniew K.
Brott, Thomas G.
Brown, Robert D.
Worrall, Bradford B.
Meschia, James F.
author_sort Ross, Owen A.
collection PubMed
description BACKGROUND: Mutations within the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). CADASIL mutations appear to be restricted to the first twenty-four exons, resulting in the gain or loss of a cysteine amino acid. The role of other exonic NOTCH3 variation not involving cysteine residues and mutations in exons 25-33 in ischemic stroke remains unresolved. METHODS: All 33 exons of NOTCH3 were sequenced in 269 Caucasian probands from the Siblings With Ischemic Stroke Study (SWISS), a 70-center North American affected sibling pair study and 95 healthy Caucasian control subjects. Variants identified by sequencing in the SWISS probands were then tested for association with ischemic stroke using US Caucasian controls collected at the Mayo Clinic (n=654), and further assessed in a Caucasian (n=802) and African American (n=298) patient-control series collected through the Ischemic Stroke Genetics Study (ISGS). RESULTS: Sequencing of the 269 SWISS probands identified one (0.4%) with small vessel type stroke carrying a known CADASIL mutation (p.R558C; Exon 11). Of the 19 common NOTCH3 variants identified, the only variant significantly associated with ischemic stroke after multiple testing adjustment was p.R1560P (rs78501403; Exon 25) in the combined SWISS and ISGS Caucasian series (Odds Ratio [OR] 0.50, P=0.0022) where presence of the minor allele was protective against ischemic stroke. Although only significant prior to adjustment for multiple testing, p.T101T (rs3815188; Exon 3) was associated with an increased risk of small-vessel stroke (OR: 1.56, P=0.008) and p.P380P (rs61749020; Exon 7) was associated with decreased risk of large-vessel stroke (OR: 0.35, P=0.047) in Caucasians. No significant associations were observed in the small African American series. CONCLUSION: Cysteine-affecting NOTCH3 mutations are rare in patients with typical ischemic stroke, however our observation that common NOTCH3 variants may be associated with risk of ischemic stroke warrants further study.
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spelling pubmed-37810282013-10-01 NOTCH3 Variants and Risk of Ischemic Stroke Ross, Owen A. Soto-Ortolaza, Alexandra I. Heckman, Michael G. Verbeeck, Christophe Serie, Daniel J. Rayaprolu, Sruti Rich, Stephen S. Nalls, Michael A. Singleton, Andrew Guerreiro, Rita Kinsella, Emma Wszolek, Zbigniew K. Brott, Thomas G. Brown, Robert D. Worrall, Bradford B. Meschia, James F. PLoS One Research Article BACKGROUND: Mutations within the NOTCH3 gene cause cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). CADASIL mutations appear to be restricted to the first twenty-four exons, resulting in the gain or loss of a cysteine amino acid. The role of other exonic NOTCH3 variation not involving cysteine residues and mutations in exons 25-33 in ischemic stroke remains unresolved. METHODS: All 33 exons of NOTCH3 were sequenced in 269 Caucasian probands from the Siblings With Ischemic Stroke Study (SWISS), a 70-center North American affected sibling pair study and 95 healthy Caucasian control subjects. Variants identified by sequencing in the SWISS probands were then tested for association with ischemic stroke using US Caucasian controls collected at the Mayo Clinic (n=654), and further assessed in a Caucasian (n=802) and African American (n=298) patient-control series collected through the Ischemic Stroke Genetics Study (ISGS). RESULTS: Sequencing of the 269 SWISS probands identified one (0.4%) with small vessel type stroke carrying a known CADASIL mutation (p.R558C; Exon 11). Of the 19 common NOTCH3 variants identified, the only variant significantly associated with ischemic stroke after multiple testing adjustment was p.R1560P (rs78501403; Exon 25) in the combined SWISS and ISGS Caucasian series (Odds Ratio [OR] 0.50, P=0.0022) where presence of the minor allele was protective against ischemic stroke. Although only significant prior to adjustment for multiple testing, p.T101T (rs3815188; Exon 3) was associated with an increased risk of small-vessel stroke (OR: 1.56, P=0.008) and p.P380P (rs61749020; Exon 7) was associated with decreased risk of large-vessel stroke (OR: 0.35, P=0.047) in Caucasians. No significant associations were observed in the small African American series. CONCLUSION: Cysteine-affecting NOTCH3 mutations are rare in patients with typical ischemic stroke, however our observation that common NOTCH3 variants may be associated with risk of ischemic stroke warrants further study. Public Library of Science 2013-09-23 /pmc/articles/PMC3781028/ /pubmed/24086431 http://dx.doi.org/10.1371/journal.pone.0075035 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Ross, Owen A.
Soto-Ortolaza, Alexandra I.
Heckman, Michael G.
Verbeeck, Christophe
Serie, Daniel J.
Rayaprolu, Sruti
Rich, Stephen S.
Nalls, Michael A.
Singleton, Andrew
Guerreiro, Rita
Kinsella, Emma
Wszolek, Zbigniew K.
Brott, Thomas G.
Brown, Robert D.
Worrall, Bradford B.
Meschia, James F.
NOTCH3 Variants and Risk of Ischemic Stroke
title NOTCH3 Variants and Risk of Ischemic Stroke
title_full NOTCH3 Variants and Risk of Ischemic Stroke
title_fullStr NOTCH3 Variants and Risk of Ischemic Stroke
title_full_unstemmed NOTCH3 Variants and Risk of Ischemic Stroke
title_short NOTCH3 Variants and Risk of Ischemic Stroke
title_sort notch3 variants and risk of ischemic stroke
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781028/
https://www.ncbi.nlm.nih.gov/pubmed/24086431
http://dx.doi.org/10.1371/journal.pone.0075035
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