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Genetic Insights on the Relation of Vascular Risk Factors and Cervical Artery Dissection

Le Grand, Q. (author)
Ferreira, L. E. (author)
Metso, T. M. (author)
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Schilling, S. (author)
Tatlisumak, Turgut (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap,Institute of Neuroscience and Physiology, Department of Clinical Neuroscience
Grond-Ginsbach, C. (author)
Engelter, S. T. (author)
Lyrer, P. (author)
Majersik, J. J. (author)
Worrall, B. B. (author)
Southerland, A. M. (author)
Markus, H. S. (author)
Lathrop, M. (author)
Thijs, V. (author)
Leys, D. (author)
Amouyel, P. (author)
Dallongeville, J. (author)
Dichgans, M. (author)
Pezzini, A. (author)
Bersano, A. (author)
Sargurupremraj, M. (author)
Debette, S. (author)
Cadisp Consortium, Cadisp Consortium (author)
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 (creator_code:org_t)
2023
2023
English.
In: Journal of the American College of Cardiology. - 0735-1097. ; 82:14, s. 1411-1423
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND The association between vascular risk factors and cervical artery dissections (CeADs), a leading cause of ischemic stroke (IS) in the young, remains controversial. OBJECTIVES 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. METHODS 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. RESULTS 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 f3-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. CONCLUSIONS 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 f3-blockers. This may inform secondary prevention strategies and trial design for CeAD. (J Am Coll Cardiol 2023;82:1411-1423) <(c)> 2023 by the American College of Cardiology Foundation.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

Keyword

KEY WORDS blood pressure
cervical artery dissection
drug effect
ischemic stroke
Mendelian randomization
young adults
Cardiovascular System & Cardiology

Publication and Content Type

ref (subject category)
art (subject category)

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