Blood biomarker changes following therapeutic hypothermia in ischemic stroke

Author:

Palà Elena1ORCID,Penalba Anna1,Bustamante Alejandro12,García‐Berrocoso Teresa13,Lamana‐Vallverdú Marcel1,Meisel Christian45,Meisel Andreas6,van der Worp H. Bart7,R Macleod Malcolm8,Kallmünzer Bernd9,Schwab Stefan9,Montaner Joan110

Affiliation:

1. Neurovascular Research Laboratory Vall d'Hebron Institute of Research (VHIR)–Universitat Autónoma de Barcelona Barcelona Spain

2. Stroke Unit, Hospital Universitari Germans Trias i Pujol Badalona Spain

3. CSIC/UAB Proteomics Laboratory Institute of Biomedical Research of Barcelona Spanish National Research Council (IIBB‐CSIC/IDIBAPS) Barcelona Spain

4. Institute for Medical Immunology Charité–Universitätsmedizin Berlin Berlin Germany

5. Department of Immunology Labor Berlin–Charité Vivantes Berlin Germany

6. Department of Neurology and Center for Stroke Research Berlin Charité University Hospital Berlin Berlin Germany

7. Department of Neurology and Neurosurgery Brain Center University Medical Center Utrecht Utrecht The Netherlands

8. Centre for Clinical Brain Sciences University of Edinburgh Edinburgh Scotland UK

9. Department of Neurology Universitätsklinikum Erlangen Erlangen Germany

10. Institute de Biomedicine of Seville, IBiS/Hospital Universitario Virgen del Rocío/CSIC/University of Seville & Department of Neurology Hospital Universitario Virgen Macarena Seville Spain

Abstract

AbstractIntroductionTherapeutic hypothermia is a promising candidate for stroke treatment although its efficacy has not yet been demonstrated in patients. Changes in blood molecules could act as surrogate markers to evaluate the efficacy and safety of therapeutic cooling.MethodsBlood samples from 54 patients included in the EuroHYP‐1 study (27 treated with hypothermia, and 27 controls) were obtained at baseline, 24 ± 2 h, and 72 ± 4 h. The levels of a panel of 27 biomarkers, including matrix metalloproteinases and cardiac and inflammatory markers, were measured.ResultsMetalloproteinase‐3 (MMP‐3), fatty‐acid‐binding protein (FABP), and interleukin‐8 (IL‐8) increased over time in relation to the hypothermia treatment. Statistically significant correlations between the minimum temperature achieved by each patient in the hypothermia group and the MMP‐3 level measured at 72 h, FABP level measured at 24 h, and IL‐8 levels measured at 24 and 72 h were found. No differential biomarker levels were observed in patients with poor or favorable outcomes according to modified Rankin Scale scores.ConclusionAlthough the exact roles of MMP3, FABP, and IL‐8 in hypothermia‐treated stroke patients are not known, further exploration is needed to confirm their roles in brain ischemia.

Funder

Instituto de Salud Carlos III

European Commission

Publisher

Wiley

Subject

Behavioral Neuroscience

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