dc.contributor.author
Liman, Thomas G.
dc.contributor.author
Siegerink, Bob
dc.contributor.author
Piper, Sophie
dc.contributor.author
Catar, Rusan
dc.contributor.author
Moll, Guido
dc.contributor.author
Riemekasten, Gabriela
dc.contributor.author
Heidecke, Harald
dc.contributor.author
Heuschmann, Peter U.
dc.contributor.author
Elkind, Mitchell S. V.
dc.contributor.author
Dragun, Duska
dc.contributor.author
Endres, Matthias
dc.date.accessioned
2025-12-04T16:49:23Z
dc.date.available
2025-12-04T16:49:23Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/50624
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-50351
dc.description.abstract
Background
Vasoregulatory autoantibodies including autoantibodies targeting G‐protein–coupled receptors might play a functional role in vascular diseases. We investigated the impact of vasoregulatory autoantibodies on clinical outcome after ischemic stroke.
Methods and Results
Data were used from the PROSCIS‐B (Prospective Cohort With Incident Stroke–Berlin). Autoantibody‐targeting receptors such as angiotensin II type 1 receptor (AT1R), endothelin‐1 type A receptor, complement factor‐3 and ‐5 receptors, vascular endothelial growth factor receptor‐1 and ‐2, vascular endothelial growth factor A and factor B were measured. We explored associations of high antibody levels with (1) poor functional outcome defined as modified Rankin Scale >2 or Barthel Index <60 at 1 year after stroke, (2) Barthel Index scores over time using general estimating equations, and (3) secondary vascular events (recurrent stroke, myocardial infarction) or death up to 3 years using Cox proportional hazard models. We included 491 patients with ischemic stroke with data on autoantibody levels and outcome. In models adjusted for demographics and vascular risk factors, high autoantibody concentrations (quartile 4) targeting complement factor C3a receptor, vascular endothelial growth factor receptor‐2, and vascular endothelial growth factor B were associated with poor functional outcome at 1 year: (odds ratio, 2.0 [95% CI, 1.1–3.6]; odds ratio, 1.8 [95% CI, 1.1–3.2]; and odds ratio, 2.1 [95% CI, 1.2–3.6], respectively) and with lower Barthel Index scores over 3 years (complement factor C3a receptor: adjusted β=−3.3 [95% CI, −5.7 to −0.5]; VEGF‐B: adjusted β=−2.4 [95% CI, −4.8 to −0.06]). Patients with high autoantibody levels were not at higher risk for secondary vascular events or death.
Conclusions
High levels of autoantibodies against vascular endothelial growth factor receptor‐2, vascular endothelial growth factor B, and complement factor C3a receptor measured are associated with poor functional outcome after stroke but not with recurrent vascular events or death.
Registration
URL: https://www.clinicaltrials.gov; Unique identifier: NCT01363856.
en
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject
autoantibodies
en
dc.subject
ischemic stroke
en
dc.subject
prospective studies
en
dc.subject
vascular endothelial growth factor A
en
dc.subject
vascular endothelial growth factor B
en
dc.subject
vascular endothelial growth factor receptor-1
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Vasoregulatory Autoantibodies and Clinical Outcome After Ischemic Stroke—PROSCIS‐B
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
e032441
dcterms.bibliographicCitation.doi
10.1161/jaha.123.032441
dcterms.bibliographicCitation.journaltitle
Journal of the American Heart Association
dcterms.bibliographicCitation.number
23
dcterms.bibliographicCitation.originalpublishername
Wiley
dcterms.bibliographicCitation.volume
12
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
DEAL Wiley
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
38014691
dcterms.isPartOf.eissn
2047-9980