Endothelial Dysfunction is Associated With Early-Onset Cryptogenic Ischemic Stroke in Men and With Increasing Age.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
20 07 2021
Historique:
pubmed: 7 7 2021
medline: 29 10 2021
entrez: 6 7 2021
Statut: ppublish

Résumé

Background The aim of this study was to assess the association between endothelial function and early-onset cryptogenic ischemic stroke (CIS), with subgroup analyses stratified by sex and age groups. Methods and Results We prospectively enrolled 136 consecutive patients aged 18 to 49 years (median age, 41 years; 44% women) with a recent CIS and 136 age- and sex-matched (±5 years) stroke-free controls. Endothelial function was measured with an EndoPAT 2000 device and analyzed as tertiles of natural logarithm of reactive hyperemia index with lower values reflecting dysfunction. We used conditional logistic regression adjusting for age, education, hypertension, diabetes mellitus, dyslipidemia, current smoking, heavy drinking, obesity, and diet score to assess the independent association between endothelial function and CIS. Patients in the lowest tertile of natural logarithm of reactive hyperemia index were more often men and they more frequently had a history of dyslipidemia; they were also more often obese, had a lower diet score, and lower high-density lipoprotein cholesterol. In the entire cohort, we found no association in patients with endothelial function and CIS compared with stroke-free controls. In sex- and age-specific analyses, endothelial dysfunction was associated with CIS in men (adjusted odds ratio [OR], 3.50 for lowest versus highest natural logarithm of reactive hyperemia index tertile; 95% CI, 1.22-10.07) and in patients ≥41 years (OR, 5.78; 95% CI, 1.52-21.95). These associations remained significant when dyslipidemia was replaced with the ratio of total to high-density lipoprotein cholesterol. Conclusions Endothelial dysfunction appears to be an independent player in early-onset CIS in men and patients approaching middle age.

Identifiants

pubmed: 34227391
doi: 10.1161/JAHA.121.020838
pmc: PMC8483459
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e020838

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Auteurs

Nicolas Martinez-Majander (N)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

Daniel Gordin (D)

Abdominal Center Nephrology University of Helsinki and Helsinki University Central Hospital Helsinki Finland.
Folkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Joslin Diabetes Center Harvard Medical School Boston MA.

Lotta Joutsi-Korhonen (L)

Coagulation Disorders Unit Department of Clinical Chemistry HUSLAB Laboratory ServicesHelsinki University Hospital Helsinki Finland.

Titta Salopuro (T)

Coagulation Disorders Unit Department of Clinical Chemistry HUSLAB Laboratory ServicesHelsinki University Hospital Helsinki Finland.

Krishna Adeshara (K)

Abdominal Center Nephrology University of Helsinki and Helsinki University Central Hospital Helsinki Finland.
Folkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.
Clinical and Molecular Metabolism Faculty of Medicine Research Programs University of Helsinki Finland.

Gerli Sibolt (G)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

Sami Curtze (S)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

Jani Pirinen (J)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.
Department of Cardiology, Heart and Lung Center Helsinki University Hospital and University of Helsinki Finland.
Department of Clinical Physiology and Nuclear Medicine HUS Medical Imaging CenterHelsinki University Central Hospital and University of Helsinki Finland.

Ron Liebkind (R)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

Lauri Soinne (L)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

Tiina Sairanen (T)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

Juha Sinisalo (J)

Department of Cardiology, Heart and Lung Center Helsinki University Hospital and University of Helsinki Finland.

Mika Lehto (M)

Department of Cardiology, Heart and Lung Center Helsinki University Hospital and University of Helsinki Finland.

Per-Henrik Groop (PH)

Abdominal Center Nephrology University of Helsinki and Helsinki University Central Hospital Helsinki Finland.
Folkhälsan Institute of GeneticsFolkhälsan Research Center Helsinki Finland.

Turgut Tatlisumak (T)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.
Department of Clinical Neuroscience Institute of Neuroscience and Physiology The Sahlgrenska Academy at University of Gothenburg Sweden.
Department of Neurology Sahlgrenska University Hospital Gothenburg Sweden.

Jukka Putaala (J)

Department of Neurology Helsinki University Hospital and Clinical NeurosciencesUniversity of Helsinki Finland.

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