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Plasmin Generation Potential and Recanalization in Acute Ischaemic Stroke; an Observational Cohort Study of Stroke Biobank Samples

Authors :
Thomas Lillicrap
Charithani B. Keragala
Dominik F. Draxler
Jilly Chan
Heidi Ho
Stevi Harman
Be'eri Niego
Elizabeth Holliday
Christopher R. Levi
Carlos Garcia-Esperon
Neil Spratt
Prajwal Gyawali
Andrew Bivard
Mark W. Parsons
Joan Montaner
Alejandro Bustamante
Israel Fernandez Cadenas
Geoffrey Cloud
Jane M. Maguire
Lisa Lincz
Timothy Kleinig
John Attia
Simon Koblar
Monica Anne Hamilton-Bruce
Philip Choi
Bradford B. Worrall
Robert L. Medcalf
National Health and Medical Research Council (Australia)
Source :
Frontiers in Neurology, Digital.CSIC. Repositorio Institucional del CSIC, instname, Frontiers in Neurology, Vol 11 (2020)
Publication Year :
2020
Publisher :
Frontiers Media SA, 2020.

Abstract

[Rationale] More than half of patients who receive thrombolysis for acute ischaemic stroke fail to recanalize. Elucidating biological factors which predict recanalization could identify therapeutic targets for increasing thrombolysis success.<br />[Hypothesis] We hypothesize that individual patient plasmin potential, as measured by in vitro response to recombinant tissue-type plasminogen activator (rt-PA), is a biomarker of rt-PA response, and that patients with greater plasmin response are more likely to recanalize early.<br />[Methods] This study will use historical samples from the Barcelona Stroke Thrombolysis Biobank, comprised of 350 pre-thrombolysis plasma samples from ischaemic stroke patients who received serial transcranial-Doppler (TCD) measurements before and after thrombolysis. The plasmin potential of each patient will be measured using the level of plasmin-antiplasmin complex (PAP) generated after in-vitro addition of rt-PA. Levels of antiplasmin, plasminogen, t-PA activity, and PAI-1 activity will also be determined. Association between plasmin potential variables and time to recanalization [assessed on serial TCD using the thrombolysis in brain ischemia (TIBI) score] will be assessed using Cox proportional hazards models, adjusted for potential confounders.<br />[Outcomes] The primary outcome will be time to recanalization detected by TCD (defined as TIBI ≥4). Secondary outcomes will be recanalization within 6-h and recanalization and/or haemorrhagic transformation at 24-h. This analysis will utilize an expanded cohort including ~120 patients from the Targeting Optimal Thrombolysis Outcomes (TOTO) study.<br />[Discussion] If association between proteolytic response to rt-PA and recanalization is confirmed, future clinical treatment may customize thrombolytic therapy to maximize outcomes and minimize adverse effects for individual patients.<br />This study was funded by competitive grants from the Australian National Health and Medical Research Council (Reference APP1085550).

Details

Language :
English
Database :
OpenAIRE
Journal :
Frontiers in Neurology, Digital.CSIC. Repositorio Institucional del CSIC, instname, Frontiers in Neurology, Vol 11 (2020)
Accession number :
edsair.doi.dedup.....2613b29a88b03844b9d5494a8dbf1ae3