Small vessel disease and biomarkers of endothelial dysfunction after ischaemic stroke.

Small vessel disease acute stroke endothelial dysfunction intercellular adhesion molecule vascular cell adhesion molecule vascular endothelial growth factor

Journal

European stroke journal
ISSN: 2396-9881
Titre abrégé: Eur Stroke J
Pays: England
ID NLM: 101688446

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 10 06 2018
accepted: 18 09 2018
entrez: 2 7 2019
pubmed: 2 7 2019
medline: 2 7 2019
Statut: ppublish

Résumé

Although pathogenesis of small vessel disease is poorly understood, increasing evidence suggests that endothelial dysfunction may have a relevant role in development and progression of small vessel disease. In this cross-sectional study, we investigated the associations between imaging signs of small vessel disease and blood biomarkers of endothelial dysfunction at two different time points in a population of ischaemic stroke patients. In stroke patients treated with intravenous thrombolysis, we analysed blood levels of von Willebrand factor, intercellular adhesion molecule-1, vascular cell adhesion molecule-1 and vascular endothelial growth factor. Three reviewers independently assessed small vessel disease features using computed tomography. At baseline and 90 days after the index stroke, we tested the associations between single and combined small vessel disease features and levels of blood biomarkers using linear regression analysis adjusting for age, sex, hypertension, diabetes, smoke. A total of 263 patients were available for the analysis. Mean age (±SD) was 69 (±13) years, 154 (59%) patients were male. We did not find any relation between small vessel disease and endothelial dysfunction at baseline. At 90 days, leukoaraiosis was independently associated with intercellular adhesion molecule-1 (β = 0.21; p = 0.016) and vascular cell adhesion molecule-1 (β = 0.22; p = 0.009), and lacunes were associated with vascular endothelial growth factor levels (β = 0.21; p = 0.009) whereas global small vessel disease burden was associated with vascular endothelial growth factor (β = 0.26; p = 0.006). Leukoaraiosis and lacunes were associated with endothelial dysfunction, which could play a key role in pathogenesis of small vessel disease. Small vessel disease features and total burden were associated with endothelial dysfunction 90 days after the stroke, whereas there was no relation during the acute phase. Our results suggest that endothelial dysfunction, particularly vascular endothelial growth factor, is involved in pathological process of small vessel disease.

Identifiants

pubmed: 31259260
doi: 10.1177/2396987318805905
pii: 10.1177_2396987318805905
pmc: PMC6591766
doi:

Types de publication

Journal Article

Langues

eng

Pagination

119-126

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Auteurs

Francesco Arba (F)

Department of NEUROFARBA, Neuroscience Section, University of Florence, Florence, Italy.
Stroke Unit, AOU Careggi, University of Florence, Florence, Italy.

Alessio Giannini (A)

Department of NEUROFARBA, Neuroscience Section, University of Florence, Florence, Italy.

Benedetta Piccardi (B)

Department of NEUROFARBA, Neuroscience Section, University of Florence, Florence, Italy.
Stroke Unit, AOU Careggi, University of Florence, Florence, Italy.

Silvia Biagini (S)

Department of NEUROFARBA, Neuroscience Section, University of Florence, Florence, Italy.

Vanessa Palumbo (V)

Stroke Unit, AOU Careggi, University of Florence, Florence, Italy.

Betti Giusti (B)

Department of Experimental and Clinical Medicine, Atherothrombotic Diseases Center, AOU Careggi, University of Florence, Florence, Italy.

Patrizia Nencini (P)

Stroke Unit, AOU Careggi, University of Florence, Florence, Italy.

Anna Maria Gori (A)

Department of Experimental and Clinical Medicine, Atherothrombotic Diseases Center, AOU Careggi, University of Florence, Florence, Italy.

Mascia Nesi (M)

Stroke Unit, AOU Careggi, University of Florence, Florence, Italy.

Giovanni Pracucci (G)

Department of NEUROFARBA, Neuroscience Section, University of Florence, Florence, Italy.

Giorgio Bono (G)

Stroke Unit, Department of Neurology, Ospedale di Circolo e Fondazione Macchi, Varese, Italy.

Paolo Bovi (P)

SSO Stroke Unit, Department of Neurosciences, Azienda Ospedaliera Integrata, Verona, Italy.

Enrico Fainardi (E)

Department of Neuroradiology, Careggi University Hospital, Florence, Italy.

Domenico Consoli (D)

U.O. Neurologia, G. Jazzolino Hospital, Vibo Valentia, Italy.

Antonia Nucera (A)

Department of Clinical Neurological Sciences, London Health Sciences Centre, Western University, London, Canada.

Francesca Massaro (F)

Neurology Unit, Santo Stefano Hospital, Prato, Italy.

Giovanni Orlandi (G)

Department of Neurosciences, Neurological Clinic, University of Pisa, Pisa, Italy.

Francesco Perini (F)

UOC di Neurologia e Stroke Unit, Ospedale San Bortolo, Vicenza, Italy.

Rossana Tassi (R)

U.O.C. Stroke Unit, Dipartimento di Scienze Neurologiche e Neurosensoriali, Azienda Ospedaliera Universitaria Senese, Siena, Italy.

Maria Sessa (M)

U.O. Neurologia, Istituti Ospitalieri di Cremona, Cremona, Italy.

Danilo Toni (D)

Emergency Department Stroke Unit, Department of Human Neurosciences, Sapienza University of Rome, Rome, Italy.

Rosanna Abbate (R)

Centro Studi Medicina Avanzata (CESMAV) Florence, Italy.

Domenico Inzitari (D)

Department of NEUROFARBA, Neuroscience Section, University of Florence, Florence, Italy.
Department of Neuroradiology, Careggi University Hospital, Florence, Italy.

Classifications MeSH