Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33923
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dc.contributor.authorLe Grand, Quentin-
dc.contributor.authorEcker Ferreira, Leslie-
dc.contributor.authorMetso, Tiina M-
dc.contributor.authorSchilling, Sabrina-
dc.contributor.authorTatlisumak, Turgut-
dc.contributor.authorGrond-Ginsbach, Caspar-
dc.contributor.authorEngelter, Stefan T-
dc.contributor.authorLyrer, Philippe-
dc.contributor.authorMajersik, Jennifer J-
dc.contributor.authorWorrall, Bradford B-
dc.contributor.authorSoutherland, Andrew M-
dc.contributor.authorMarkus, Hugh S-
dc.contributor.authorLathrop, Mark-
dc.contributor.authorThijs, Vincent N-
dc.contributor.authorLeys, Didier-
dc.contributor.authorAmouyel, Philippe-
dc.contributor.authorDallongeville, Jean-
dc.contributor.authorDichgans, Martin-
dc.contributor.authorPezzini, Alessandro-
dc.contributor.authorBersano, Anna-
dc.contributor.authorSargurupremraj, Muralidharan-
dc.contributor.authorDebette, Stéphanie-
dc.date.accessioned2023-10-04T02:43:35Z-
dc.date.available2023-10-04T02:43:35Z-
dc.date.issued2023-10-03-
dc.identifier.citationJournal of the American College of Cardiology 2023-10-03; 82(14)en_US
dc.identifier.issn1558-3597-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33923-
dc.description.abstractThe association between vascular risk factors and cervical artery dissections (CeADs), a leading cause of ischemic stroke (IS) in the young, remains controversial. This study aimed to explore the causal relation of vascular risk factors with CeAD risk and recurrence and compare it to their relation with non-CeAD IS. This study used 2-sample Mendelian randomization analyses to explore the association of blood pressure (BP), lipid levels, type 2 diabetes, waist-to-hip ratio, smoking, and body mass index with CeAD and non-CeAD IS. To simulate effects of the most frequently used BP-lowering drugs, this study constructed genetic proxies and tested their association with CeAD and non-CeAD IS. In analyses among patients with CeAD, the investigators studied the association between weighted genetic risk scores of vascular risk factors and the risk of multiple or early recurrent dissections. Genetically determined higher systolic BP (OR: 1.51; 95% CI: 1.32-1.72) and diastolic BP (OR: 2.40; 95% CI: 1.92-3.00) increased the risk of CeAD (P < 0.0001). Genetically determined higher body mass index was inconsistently associated with a lower risk of CeAD. Genetic proxies for β-blocker effects were associated with a lower risk of CeAD (OR: 0.65; 95% CI: 0.50-0.85), whereas calcium-channel blockers were associated with a lower risk of non-CeAD IS (OR: 0.75; 95% CI: 0.63-0.90). Weighted genetic risk scores for systolic BP and diastolic BP were associated with an increased risk of multiple or early recurrent CeAD. These results are supportive of a causal association between higher BP and increased CeAD risk and recurrence and provide genetic evidence for lower CeAD risk under β-blockers. This may inform secondary prevention strategies and trial design for CeAD.en_US
dc.language.isoeng-
dc.subjectMendelian randomizationen_US
dc.subjectblood pressureen_US
dc.subjectcervical artery dissectionen_US
dc.subjectdrug effecten_US
dc.subjectischemic strokeen_US
dc.subjectyoung adultsen_US
dc.titleGenetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of the American College of Cardiologyen_US
dc.identifier.affiliationUniversity of Bordeaux, Institut National de la Santé et de la Recherche Médicale (INSERM), Bordeaux Population Health Center (BPH), Unité Mixte de Recherche (U) 1219, Bordeaux, France.en_US
dc.identifier.affiliationDepartment of Medicine and Joinville Stroke Biobank, University of Region of Joinville, Joinville, Brazil.en_US
dc.identifier.affiliationDepartment of Neurology, Helsinki University Central Hospital, Helsinki, Finland.en_US
dc.identifier.affiliationUniversity of Bordeaux, Institut National de la Santé et de la Recherche Médicale (INSERM), Bordeaux Population Health Center (BPH), Unité Mixte de Recherche (U) 1219, Bordeaux, France.en_US
dc.identifier.affiliationDepartment of Clinical Neurosciences/Neurology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden; Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.en_US
dc.identifier.affiliationDepartment of Vascular and Endovascular Surgery, University of Heidelberg, Heidelberg, Germany.en_US
dc.identifier.affiliationNeurology and Neurorehabilitation, University Department of Geriatric Medicine Felix Platter, University of Basel, Basel, Switzerland; Department of Neurology and Stroke Center, University Hospital Basel, University of Basel, Basel, Switzerland.en_US
dc.identifier.affiliationDepartment of Neurology and Stroke Center, University Hospital Basel, University of Basel, Basel, Switzerland.en_US
dc.identifier.affiliationDepartment of Neurology, University of Utah, Salt Lake City, Utah, USA.en_US
dc.identifier.affiliationDepartment of Neurology, University of Virginia, Charlottesville, Virginia, USA; Department of Public Health Sciences, University of Virginia, Charlottesville, Virginia, USA.en_US
dc.identifier.affiliationStroke Research Group, Department of Clinical Neurosciences, University of Cambridge, Cambridge Biomedical Campus, Cambridge, United Kingdom.en_US
dc.identifier.affiliationDepartment of Human Genetics, McGill University, Montreal, Quebec, Canada; Victor Phillip Dahdaleh Institute of Genomic Medicine at McGill University, Montreal, Quebec, Canada.en_US
dc.identifier.affiliationStroke Division, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, Victoria, Australia; Department of Neurology, Austin Health, Melbourne, Victoria, Australia.en_US
dc.identifier.affiliationINSERM U1172, Lille Neuroscience and Cognition, University of Lille, Lille, France.en_US
dc.identifier.affiliationLaboratory of Excellence Development of Innovative Strategies for a Transdisciplinary Approach to Alzheimer's Disease (LabEx DISTALZ), University of Lille, Lille, France; INSERM U1167 (Risk Factors and Molecular Determinants of Aging-Related Diseases - RID-AGE), Lille, France; Centre Hospitalier Universitaire Lille, Lille, France; Institut Pasteur de Lille, Lille, France.en_US
dc.identifier.affiliationInstitute for Stroke and Dementia Research, University Hospital, Ludwig-Maximilians University Munich, Munich, Germany; Munich Cluster for Systems Neurology, Munich, Germany; German Center for Neurodegenerative Diseases, Munich, Germany.en_US
dc.identifier.affiliationDepartment of Clinical and Experimental Sciences, Neurology Unit, University of Brescia, Brescia, Italy.en_US
dc.identifier.affiliationCerebrovascular Unit, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Istituto Neurologico Carlo Besta, Milan, Italy.en_US
dc.identifier.affiliationNeurologyen_US
dc.identifier.affiliationUniversity of Bordeaux, Institut National de la Santé et de la Recherche Médicale (INSERM), Bordeaux Population Health Center (BPH), Unité Mixte de Recherche (U) 1219, Bordeaux, France; Department of Neurology, Institute of Neurodegenerative Diseases, Bordeaux University Hospital, Bordeaux, France.en_US
dc.identifier.doi10.1016/j.jacc.2023.07.021en_US
dc.type.contentTexten_US
dc.identifier.pubmedid37758436-
dc.description.volume82-
dc.description.issue14-
dc.description.startpage1411-
dc.description.endpage1423-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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