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Antihypertensives and Statin Therapy for Primary Stroke Prevention: A Secondary Analysis of the HOPE-3 Tria

  • Jackie Bosch*
  • , Eva M. Lonn
  • , Gilles R. Dagenais
  • , Peggy Gao
  • , Patricio Lopez-Jaramillo
  • , Jun Zhu
  • , Prem Pais
  • , Alvaro Avezum
  • , Karen Sliwa
  • , Irina E. Chazova
  • , Ron J. G. Peters
  • , Claes Held
  • , Khalid Yusoff
  • , Basil S. Lewis
  • , William D. Toff
  • , Kamlesh Khunti
  • , Christopher M. Reid
  • , Lawrence A. Leiter
  • , Salim Yusuf
  • , Robert G. Hart
  • *Corresponding author for this work
  • Hamilton Health Sciences
  • McMaster University
  • Université Laval
  • Instituto Masira Facultad de Salud Universidad de Santander Bucaramanga Colombia
  • Chinese Academy of Medical Sciences
  • St. John's National Academy of Health Sciences
  • Instituto Dante Pazzanese de Cardiologia
  • University of Cape Town
  • RAS - USSR Cardiology Research Center
  • Amsterdam UMC - University of Amsterdam
  • Uppsala University
  • Universiti Teknologi Majlis Amansh Rakyat Selayang Malaysia (K.Y.).
  • UCSI University
  • Technion-Israel Institute of Technology
  • University Hospitals of Leicester NHS Trust
  • University of Leicester
  • Curtin University
  • Monash University
  • The Keenan Research Centre for Biomedical Science, St Michael's Hospital, Toronto, Ontario, Canada

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Abstract

Background and Purpose: The HOPE-3 trial (Heart Outcomes Prevention Evaluation-3) found that antihypertensive therapy combined with a statin reduced first stroke among people at intermediate cardiovascular risk. We report secondary analyses of stroke outcomes by stroke subtype, predictors, treatment effects in key subgroups. Methods: Using a 2-by-2 factorial design, 12 705 participants from 21 countries with vascular risk factors but without overt cardiovascular disease were randomized to candesartan 16 mg plus hydrochlorothiazide 12.5 mg daily or placebo and to rosuvastatin 10 mg daily or placebo. The effect of the interventions on stroke subtypes was assessed. Results: Participants were 66 years old and 46% were women. Baseline blood pressure (138/82 mm Hg) was reduced by 6.0/3.0 mm Hg and LDL-C (low-density lipoprotein cholesterol; 3.3 mmol/L) was reduced by 0.90 mmol/L on active treatment. During 5.6 years of follow-up, 169 strokes occurred (117 ischemic, 29 hemorrhagic, 23 undetermined). Blood pressure lowering did not significantly reduce stroke (hazard ratio [HR], 0.80 [95% CI, 0.59-1.08]), ischemic stroke (HR, 0.80 [95% CI, 0.55-1.15]), hemorrhagic stroke (HR, 0.71 [95% CI, 0.34-1.48]), or strokes of undetermined origin (HR, 0.92 [95% CI, 0.41-2.08]). Rosuvastatin significantly reduced strokes (HR, 0.70 [95% CI, 0.52-0.95]), with reductions mainly in ischemic stroke (HR, 0.53 [95% CI, 0.37-0.78]) but did not significantly affect hemorrhagic (HR, 1.22 [95% CI, 0.59-2.54]) or strokes of undetermined origin (HR, 1.29 [95% CI, 0.57-2.95]). The combination of both interventions compared with double placebo substantially and significantly reduced strokes (HR, 0.56 [95% CI, 0.36-0.87]) and ischemic strokes (HR, 0.41 [95% CI, 0.23-0.72]). Conclusions: Among people at intermediate cardiovascular risk but without overt cardiovascular disease, rosuvastatin 10 mg daily significantly reduced first stroke. Blood pressure lowering combined with rosuvastatin reduced ischemic stroke by 59%. Both therapies are safe and generally well tolerated. Registration: URL: Https://www.clinicaltrials.gov; Unique identifier: NCT00468923.
Original languageEnglish
Pages (from-to)2494-2501
Number of pages8
JournalStroke
Volume52
Issue number8
Early online date2021
DOIs
Publication statusPublished - Aug 2021

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • blood pressure
  • candesartan
  • cardiovascular disease
  • lipoprotein
  • primary prevention
  • statin

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