Endotheliitis and cytokine storm as a mechanism of clot formation in COVID-19 ischemic stroke patients: A histopathologic study of retrieved clots.

COVID-19 emboli ischemic stroke mechanism

Journal

Interventional neuroradiology : journal of peritherapeutic neuroradiology, surgical procedures and related neurosciences
ISSN: 2385-2011
Titre abrégé: Interv Neuroradiol
Pays: United States
ID NLM: 9602695

Informations de publication

Date de publication:
28 Sep 2023
Historique:
medline: 29 9 2023
pubmed: 29 9 2023
entrez: 28 9 2023
Statut: aheadofprint

Résumé

Studies during the COVID-19 pandemic have demonstrated an association between COVID-19 virus infection and the development of acute ischemic stroke, particularly large vessel occlusion (LVO). Studying the characteristics and immunohistochemistry of retrieved stroke emboli during mechanical thrombectomy for LVO may offer insights into the pathogenesis of LVO in COVID-19 patients. We examined retrieved COVID-19 emboli from the STRIP, EXCELLENT, and RESTORE registries and compared their characteristics to a control group. We identified COVID-positive LVO patients from the STRIP, RESTORE, and EXCELLENT studies who underwent mechanical thrombectomy. These patients were matched to a control group controlling for stroke etiology based on Trial of Org 10172 in Acute Stroke Treatment criteria. All clots were stained with Martius Scarlet Blue (MSB) along with immunohistochemistry for interleukin-6 (IL-6), C-reactive protein (CRP), von Willebrand factor (vWF), CD66b, fibrinogen, and citrullinated Histone H3. Clot composition was compared between groups. Nineteen COVID-19-positive patients and 38 controls were included. COVID-19-positive patients had a significantly higher percentage of CRP and vWF. There was no difference in IL-6, fibrin, CD66b, or citrullinated Histone H3 between groups. Based on MSB staining, there was no statistically significant difference regarding the percentage of red blood cells, white blood cells, fibrin, and platelets. Our study found higher concentrations of CRP and vWF in retrieved clots of COVID-19-positive stroke patients compared to COVID-19-negative controls. These findings support the potential role of systemic inflammation as indicated by elevated CRP and endothelial injury as indicated by elevated vWF as precipitating factors in thrombus development in these patients.

Sections du résumé

BACKGROUND BACKGROUND
Studies during the COVID-19 pandemic have demonstrated an association between COVID-19 virus infection and the development of acute ischemic stroke, particularly large vessel occlusion (LVO). Studying the characteristics and immunohistochemistry of retrieved stroke emboli during mechanical thrombectomy for LVO may offer insights into the pathogenesis of LVO in COVID-19 patients. We examined retrieved COVID-19 emboli from the STRIP, EXCELLENT, and RESTORE registries and compared their characteristics to a control group.
METHODS METHODS
We identified COVID-positive LVO patients from the STRIP, RESTORE, and EXCELLENT studies who underwent mechanical thrombectomy. These patients were matched to a control group controlling for stroke etiology based on Trial of Org 10172 in Acute Stroke Treatment criteria. All clots were stained with Martius Scarlet Blue (MSB) along with immunohistochemistry for interleukin-6 (IL-6), C-reactive protein (CRP), von Willebrand factor (vWF), CD66b, fibrinogen, and citrullinated Histone H3. Clot composition was compared between groups.
RESULTS RESULTS
Nineteen COVID-19-positive patients and 38 controls were included. COVID-19-positive patients had a significantly higher percentage of CRP and vWF. There was no difference in IL-6, fibrin, CD66b, or citrullinated Histone H3 between groups. Based on MSB staining, there was no statistically significant difference regarding the percentage of red blood cells, white blood cells, fibrin, and platelets.
CONCLUSIONS CONCLUSIONS
Our study found higher concentrations of CRP and vWF in retrieved clots of COVID-19-positive stroke patients compared to COVID-19-negative controls. These findings support the potential role of systemic inflammation as indicated by elevated CRP and endothelial injury as indicated by elevated vWF as precipitating factors in thrombus development in these patients.

Identifiants

pubmed: 37769315
doi: 10.1177/15910199231185804
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

15910199231185804

Auteurs

Waleed Brinjikji (W)

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

David F Kallmes (DF)

Department of Radiology, Mayo Clinic, Rochester, MN, USA.

Renu Virmani (R)

Department of Pathology, CVPath Institute, Gaithersburg, MD, USA.

Simon F de Meyer (SF)

Laboratory for Thrombosis Research, KU Leuven Campus Kulak Kortrijk, Kortrijk, Belgium.

Albert J Yoo (AJ)

Neurointervention, Texas Stroke Institute, Plano, TX, USA.

William Humphries (W)

Wellstar Health System, Kennestone Hospital, Marietta, GA, USA.

Osama O Zaidat (OO)

Department of Neuroscience, Mercy Health St Vincent Medical Center, Toledo, OH, USA.

Mohamed S Teleb (MS)

Neurointerventional Surgery, Stroke, and Neurocritical Care, Banner Health, Mesa, AZ, USA.

Jesse G Jones (JG)

Department of Neurosurgery, University of Alabama, Birmingham, AL, USA.

Adnan H Siddiqui (AH)

Departments of Neurosurgery and Radiology, State University of New York at Buffalo, New York, NY, USA.

Tommy Andersson (T)

Department of Neuroradiology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.

Raul G Nogueira (RG)

Department of Neurology and Neurosurgery, University of Pittsburgh Medical Center, UPMC Stroke Institute, Pittsburgh, PA, USA.

Sara Molina Gil (SM)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland, Galway, Ireland.
CÚRAM-SFI Research Centre for Medical Devices, National University of Ireland Galway, Galway, Ireland.

Andrew Douglas (A)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland, Galway, Ireland.
CÚRAM-SFI Research Centre for Medical Devices, National University of Ireland Galway, Galway, Ireland.

Rosanna Rossi (R)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland, Galway, Ireland.
CÚRAM-SFI Research Centre for Medical Devices, National University of Ireland Galway, Galway, Ireland.

Alexander Rentzos (A)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Erik Ceder (E)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Jeanette Carlqvist (J)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Dennis Dunker (D)

Department of Interventional and Diagnostic Neuroradiology, Sahlgrenska University Hospital, University of Gothenburg, Gothenburg, Sweden.

Katarina Jood (K)

Department of Clinical Neurosciences, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Turgut Tatlisumak (T)

Department of Clinical Neurosciences, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.
Department of Neurology, Sahlgrenska University Hospital, Gothenburg, Sweden.

Karen M Doyle (KM)

Department of Physiology and Galway Neuroscience Centre, School of Medicine, National University of Ireland, Galway, Ireland.
CÚRAM-SFI Research Centre for Medical Devices, National University of Ireland Galway, Galway, Ireland.

Classifications MeSH