Blood pressure variability in acute stroke: Risk factors and association with functional outcomes at 1 month.

blood pressure blood pressure variability functional outcomes sodium stroke

Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
13 May 2024
Historique:
revised: 02 04 2024
received: 21 02 2024
accepted: 08 04 2024
medline: 13 5 2024
pubmed: 13 5 2024
entrez: 13 5 2024
Statut: aheadofprint

Résumé

Blood pressure variability, in acute stroke, may be an important modifiable determinant of functional outcome after stroke. In a large international cohort of participants with acute stroke, it was sought to determine the association of blood pressure variability (in the early period of admission) and functional outcomes, and to explore risk factors for increased blood pressure variability. INTERSTROKE is an international case-control study of risk factors for first acute stroke. Blood pressure was recorded at the time of admission, the morning after admission and the time of interview in cases (median time from admission 36.7 h). Multivariable ordinal regression analysis was employed to determine the association of blood pressure variability (standard deviation [SD] and coefficient of variance) with modified Rankin score at 1-month follow-up, and logistic regression was used to identify risk factors for blood pressure variability. Amongst 13,206 participants, the mean age was 62.19 ± 13.58 years. When measured by SD, both systolic blood pressure variability (odds ratio 1.13; 95% confidence interval 1.03-1.24 for SD ≥20 mmHg) and diastolic blood pressure variability (odds ratio 1.15; 95% confidence interval 1.04-1.26 for SD ≥10 mmHg) were associated with a significant increase in the odds of poor functional outcome. The highest coefficient of variance category was not associated with a significant increase in risk of higher modified Rankin score at 1 month. Increasing age, female sex, high body mass index, history of hypertension, alcohol use, and high urinary potassium and low urinary sodium excretion were associated with increased blood pressure variability. Increased blood pressure variability in acute stroke, measured by SD, is associated with an increased risk of poor functional outcome at 1 month. Potentially modifiable risk factors for increased blood pressure variability include low urinary sodium excretion.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
Blood pressure variability, in acute stroke, may be an important modifiable determinant of functional outcome after stroke. In a large international cohort of participants with acute stroke, it was sought to determine the association of blood pressure variability (in the early period of admission) and functional outcomes, and to explore risk factors for increased blood pressure variability.
PATIENTS AND METHODS METHODS
INTERSTROKE is an international case-control study of risk factors for first acute stroke. Blood pressure was recorded at the time of admission, the morning after admission and the time of interview in cases (median time from admission 36.7 h). Multivariable ordinal regression analysis was employed to determine the association of blood pressure variability (standard deviation [SD] and coefficient of variance) with modified Rankin score at 1-month follow-up, and logistic regression was used to identify risk factors for blood pressure variability.
RESULTS RESULTS
Amongst 13,206 participants, the mean age was 62.19 ± 13.58 years. When measured by SD, both systolic blood pressure variability (odds ratio 1.13; 95% confidence interval 1.03-1.24 for SD ≥20 mmHg) and diastolic blood pressure variability (odds ratio 1.15; 95% confidence interval 1.04-1.26 for SD ≥10 mmHg) were associated with a significant increase in the odds of poor functional outcome. The highest coefficient of variance category was not associated with a significant increase in risk of higher modified Rankin score at 1 month. Increasing age, female sex, high body mass index, history of hypertension, alcohol use, and high urinary potassium and low urinary sodium excretion were associated with increased blood pressure variability.
CONCLUSION CONCLUSIONS
Increased blood pressure variability in acute stroke, measured by SD, is associated with an increased risk of poor functional outcome at 1 month. Potentially modifiable risk factors for increased blood pressure variability include low urinary sodium excretion.

Identifiants

pubmed: 38738545
doi: 10.1111/ene.16314
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e16314

Subventions

Organisme : CIHR
Pays : Canada

Informations de copyright

© 2024 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.

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Auteurs

Catriona Reddin (C)

HRB Clinical Research Facility Galway, School of Medicine, University of Galway, Galway, Ireland.
Wellcome Trust-HRB, Irish Clinical Academic Training, Dublin, Ireland.

Robert Murphy (R)

HRB Clinical Research Facility Galway, School of Medicine, University of Galway, Galway, Ireland.

Graeme J Hankey (GJ)

Perron Institute Chair in Stroke Research, Medical School, University of Western Australia, Perth, Western Australia, Australia.
Perron Institute for Neurological and Translational Science, Perth, Western Australia, Australia.

Xingyu Wang (X)

Beijing Hypertension League Institute, Beijing, China.

Peter Langhorne (P)

Academic Section of Geriatric Medicine, Glasgow Royal Infirmary, University of Glasgow, Glasgow, UK.

Shahram Oveisgharan (S)

Rush Alzheimer Disease Research Center, Rush University Medical Center, Chicago, Illinois, USA.

Denis Xavier (D)

St Johns Medical College, Bangalore, India.
St Johns Research Institute, Bangalore, India.

Conor Judge (C)

HRB Clinical Research Facility Galway, School of Medicine, University of Galway, Galway, Ireland.

Annika Rosengren (A)

Sahlgrenska University Hospital and Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Helle K Iversen (HK)

Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Anna Czlonkowska (A)

Institute of Psychiatry and Neurology, Warsaw, Poland.

Fernando Lanas (F)

Faculty of Medicine, Universidad de La Frontera, Temuco, Chile.

Aytekin Oguz (A)

Department of Internal Medicine, Faculty of Medicine, Istanbul Medeniyet University, Dumlupinar Mahallesi, Istanbul, Turkey.
Faculty of Medicine, Istanbul Medeniyet University, Istanbul, Turkey.

Danuta Ryglewicz (D)

Military Institute of Aviation Medicine, Warszawa, Poland.

Mohammad Wasay (M)

Department of Medicine, Aga Khan University, Karachi, Pakistan.

Andrew Smyth (A)

HRB Clinical Research Facility Galway, School of Medicine, University of Galway, Galway, Ireland.

Salim Yusuf (S)

Population Health Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, Ontario, Canada.

Martin O'Donnell (M)

HRB Clinical Research Facility Galway, School of Medicine, University of Galway, Galway, Ireland.
Population Health Research Institute, Hamilton Health Sciences and McMaster University, Hamilton, Ontario, Canada.

Classifications MeSH