Circulating levels of vascular endothelial growth factor and post-stroke long-term functional outcome.


Journal

Acta neurologica Scandinavica
ISSN: 1600-0404
Titre abrégé: Acta Neurol Scand
Pays: Denmark
ID NLM: 0370336

Informations de publication

Date de publication:
May 2020
Historique:
received: 11 10 2019
revised: 23 12 2019
accepted: 05 01 2020
pubmed: 11 1 2020
medline: 25 8 2020
entrez: 11 1 2020
Statut: ppublish

Résumé

Vascular endothelial growth factor (VEGF) acts in angiogenesis and neuroprotection, although the beneficial effects on experimental ischemic stroke (IS) have not been replicated in clinical studies. We investigated serum VEGF (s-VEGF) in the acute stage (baseline) and 3 months post-stroke in relation to stroke severity and functional outcome. The s-VEGF and serum high-sensitivity C-reactive protein (hs-CRP) concentrations were measured in patients enrolled in the Sahlgrenska Academy Study on Ischemic Stroke (SAHLSIS) at the acute time-point (median 4 days, N = 492, 36% female; mean age, 57 years) and at 3 months post-stroke (N = 469). Baseline stroke severity was classified according to the National Institutes of Health Stroke Scale (NIHSS), and functional outcomes (3 months and 2 years) were evaluated using the modified Rankin Scale (mRS), dichotomized into good (mRS 0-2), and poor (mRS 3-6) outcomes. Multivariable logistic regression analyses were adjusted for covariates. The baseline s-VEGF did not correlate with stroke severity but correlated moderately with hs-CRP (r = .17, P < .001). The baseline s-VEGF was 39.8% higher in total anterior cerebral infarctions than in lacunar cerebral infarctions. In binary logistic regression analysis, associations with 3-month functional outcome were non-significant. However, an association between the 3-month s-VEGF and poor 2-year outcome withstood adjustments for age, sex, cardiovascular covariates, and stroke severity (per 10-fold increase in s-VEGF, odds ratio [OR], 2.56, 95% confidence interval [CI] 1.12-5.82) or hs-CRP (OR 2.53, CI 1.15-5.55). High 3-month s-VEGF is independently associated with poor 2-year functional outcome but not with 3-month outcome.

Identifiants

pubmed: 31919840
doi: 10.1111/ane.13219
doi:

Substances chimiques

VEGFA protein, human 0
Vascular Endothelial Growth Factor A 0
C-Reactive Protein 9007-41-4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

405-414

Subventions

Organisme : John och Brit Wennerströms Stiftelse för Neurologisk Forskning
Organisme : Stiftelsen Lars Hiertas Minne
Organisme : Magnus Bergvalls Stiftelse
Organisme : The Swedish Heart Lung Foundation
ID : 20160316
Organisme : The European Research Council
ID : 681712
Organisme : Edit Jacobson Foundation
Organisme : Emelle Foundation
Organisme : The Yngve Land Foundation
Organisme : The Swedish Stroke Association
Organisme : Grants the Swedish state under the agreement between the Swedish government (ALF agreement)
ID : ALFGBG-720081; -147771; -722371; -715986; -720931
Organisme : Svenska Läkaresällskapet
Organisme : Vetenskapsrådet
ID : 2018-02542
Organisme : The Göteborg Foundation for Neurological Research
Organisme : Rune och Ulla Amlövs Stiftelse för Neurologisk och Reumatologisk Forskning
Organisme : The Torsten Söderberg Foundation
Organisme : Hjärnfonden
ID : FO2017-0243

Informations de copyright

© 2020 The Authors. Acta Neurologica Scandinavica published by John Wiley & Sons Ltd.

Références

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Auteurs

N David Åberg (ND)

Department of Internal Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

Alexander Wall (A)

Department of Internal Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

Olof Anger (O)

Department of Internal Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

Katarina Jood (K)

Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.
Department for Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Ulf Andreasson (U)

Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.

Kaj Blennow (K)

Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.

Henrik Zetterberg (H)

Clinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, Sweden.
Department of Psychiatry and Neurochemistry, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Mölndal, Sweden.
Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK.
UK Dementia Research Institute at UCL, London, UK.

Jörgen Isgaard (J)

Department of Internal Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

Christina Jern (C)

Department of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.

Johan Svensson (J)

Department of Internal Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Region Västra Götaland, Sahlgrenska University Hospital, Gothenburg, Sweden.

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