Homoarginine Associates with Carotid Intima-Media Thickness and Atrial Fibrillation and Predicts Adverse Events after Stroke.

acute stroke atrial fibrillation carotid intima-media thickness homoarginine transient ischemic attack

Journal

Life (Basel, Switzerland)
ISSN: 2075-1729
Titre abrégé: Life (Basel)
Pays: Switzerland
ID NLM: 101580444

Informations de publication

Date de publication:
20 Jul 2023
Historique:
received: 06 06 2023
revised: 13 07 2023
accepted: 17 07 2023
medline: 29 7 2023
pubmed: 29 7 2023
entrez: 29 7 2023
Statut: epublish

Résumé

Homoarginine is associated with cardio- and cerebrovascular morbidity and mortality. However, the underlying pathomechanisms remain elusive. Here, we evaluated the association of homoarginine with adverse events (i.e., death, stroke, and myocardial infarction) and carotid intima-media thickness (cIMT) in stroke patients. In the prospective bioMARKers in STROKE (MARK-STROKE) cohort, patients with acute ischemic stroke or transient ischemic attack (TIA) were enrolled. Plasma homoarginine concentrations were analyzed and associated with clinical phenotypes in cross-sectional (374 patients) and prospective (273 patients) analyses. Adjustments for possible confounders were evaluated. A two-fold increase in homoarginine was inversely associated with the National Institutes of Health Stroke Scale (NIHSS) score at admission, cIMT, and prevalent atrial fibrillation (mean factor -0.68 [95% confidence interval (CI): -1.30, -0.07], -0.14 [95% CI: -0.22, -0.05]; and odds ratio 0.57 [95% CI: 0.33, 0.96], respectively). During the follow-up (median 284 [25th, 75th percentile: 198, 431] days), individuals with homoarginine levels in the highest tertile had fewer incident events compared with patients in the lowest homoarginine tertile independent of traditional risk factors (hazard ratio 0.22 [95% CI: 0.08, 0.63]). A lower prevalence of atrial fibrillation and a reduced cIMT pinpointed potential underlying pathomechanisms.

Identifiants

pubmed: 37511965
pii: life13071590
doi: 10.3390/life13071590
pmc: PMC10381763
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Else Kröner-Fresenius-Stiftung
ID : 2018_EKES.04
Organisme : Else Kröner-Fresenius-Stiftung
ID : 2020 EKES.16

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Auteurs

Laura Schwieren (L)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
Institute of Clinical Pharmacology and Toxicology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Märit Jensen (M)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Robert Schulz (R)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Susanne Lezius (S)

Institute of Medical Biometry and Epidemiology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Elena Laxy (E)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Magalie Milatz (M)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Götz Thomalla (G)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Rainer Böger (R)

Institute of Clinical Pharmacology and Toxicology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Christian Gerloff (C)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Tim Magnus (T)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Edzard Schwedhelm (E)

Institute of Clinical Pharmacology and Toxicology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.
German Centre for Cardiovascular Research (DZHK e.V.) Partner Site Hamburg/Kiel/Lübeck, 20246 Hamburg, Germany.

Chi-Un Choe (CU)

Department of Neurology, University Medical Centre Hamburg-Eppendorf, 20246 Hamburg, Germany.

Classifications MeSH