The TAXINOMISIS Project: A multidisciplinary approach for the development of a new risk stratification model for patients with asymptomatic carotid artery stenosis

Introduction Asymptomatic carotid artery stenosis (ACAS) may cause future stroke and therefore patients with ACAS require best medical treatment. Patients at high risk for stroke may opt for additional revascularization (either surgery or stenting) but the future stroke risk should outweigh the risk...

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Veröffentlicht in:European journal of clinical investigation 2020-12, Vol.50 (12), p.e13411-n/a
Hauptverfasser: Timmerman, Nathalie, Galyfos, George, Sigala, Fragiska, Thanopoulou, Kalliopi, de Borst, Gert J., Davidovic, Lazar, Eckstein, Hans‐Henning, Filipovic, Nenad, Grugni, Roberto, Kallmayer, Michael, de Kleijn, Dominique P. V., Koncar, Igor, Mantzaris, Michalis D., Marchal, Elisabeth, Matsagkas, Miltiadis, Mutavdzic, Perica, Palombo, Domenico, Pasterkamp, Gerard, Potsika, Vassiliki T., Andreakos, Evangelos, Fotiadis, Dimitrios I.
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Sprache:eng
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Zusammenfassung:Introduction Asymptomatic carotid artery stenosis (ACAS) may cause future stroke and therefore patients with ACAS require best medical treatment. Patients at high risk for stroke may opt for additional revascularization (either surgery or stenting) but the future stroke risk should outweigh the risk for peri/post‐operative stroke/death. Current risk stratification for patients with ACAS is largely based on outdated randomized‐controlled trials that lack the integration of improved medical therapies and risk factor control. Furthermore, recent circulating and imaging biomarkers for stroke have never been included in a risk stratification model. The TAXINOMISIS Project aims to develop a new risk stratification model for cerebrovascular complications in patients with ACAS and this will be tested through a prospective observational multicentre clinical trial performed in six major European vascular surgery centres. Methods and analysis The risk stratification model will compromise clinical, circulating, plaque and imaging biomarkers. The prospective multicentre observational study will include 300 patients with 50%‐99% ACAS. The primary endpoint is the three‐year incidence of cerebrovascular complications. Biomarkers will be retrieved from plasma samples, brain MRI, carotid MRA and duplex ultrasound. The TAXINOMISIS Project will serve as a platform for the development of new computer tools that assess plaque progression based on radiology images and a lab‐on‐chip with genetic variants that could predict medication response in individual patients. Conclusion Results from the TAXINOMISIS study could potentially improve future risk stratification in patients with ACAS to assist personalized evidence‐based treatment decision‐making.
ISSN:0014-2972
1365-2362
DOI:10.1111/eci.13411