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Effects of blood pressure and lipid lowering on cognition: Results from the HOPE-3 study

  • Jackie Bosch
  • , Martin O'donnell
  • , Balakumar Swaminathan
  • , Eva Marie Lonn
  • , Mikul Sharma
  • , Gilles Dagenais
  • , Rafael Diaz
  • , Kamlesh Khunti
  • , Basil S. Lewis
  • , Alvaro Avezum
  • , Claes Held
  • , Matyas Keltai
  • , Christopher Reid
  • , William D. Toff
  • , Antonio Dans
  • , Lawrence A. Leiter
  • , Karen Sliwa
  • , Shun Fu Lee
  • , Janice M. Pogue
  • , Robert Hart
  • Salim Yusuf
  • Population Health Research Institute, Ontario
  • McMaster University
  • Institut Universitaire de Cardiologie et de Pneumologie de Québec
  • Instituto Cardiovascular de Rosario
  • University of Leicester
  • Technion - Israel Institute of Technology
  • Dante Pazzanese Institute of Cardiology
  • Uppsala University
  • Semmelweis University
  • Monash University
  • Curtin University
  • University of Leicester General Hospital
  • University of the Philippines Manila
  • Li Ka Shing Knowledge Institute
  • University of Cape Town

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

84 Citations (Scopus)

Abstract

ObjectiveTo assess whether long-term treatment with candesartan/hydrochlorothiazide, rosuvastatin, or their combination can slow cognitive decline in older people at intermediate cardiovascular risk.MethodsThe Heart Outcomes Prevention Evaluation-3 (HOPE-3) study was a double-blind, randomized, placebo-controlled clinical trial using a 2 × 2 factorial design. Participants without known cardiovascular disease or need for treatment were randomized to candesartan (16 mg) plus hydrochlorothiazide (12.5 mg) or placebo and to rosuvastatin (10 mg) or placebo. Participants who were ≥70 years of age completed the Digit Symbol Substitution Test (DSST), the modified Montreal Cognitive Assessment, and the Trail Making Test Part B at baseline and study end.ResultsCognitive assessments were completed by 2,361 participants from 228 centers in 21 countries. Compared with placebo, candesartan/hydrochlorothiazide reduced systolic blood pressure by 6.0 mm Hg, and rosuvastatin reduced low-density lipoprotein cholesterol by 24.8 mg/dL. Participants were followed up for 5.7 years (median), and 1,626 completed both baseline and study-End assessments. Mean participant age was 74 years (SD ±3.5 years); 59% were women; 45% had hypertension; and 24% had ≥12 years of education. The mean difference in change in DSST scores was -0.91 (95% confidence interval [CI] -2.25 to 0.42) for candesartan/hydrochlorothiazide compared with placebo, -0.54 (95% CI -1.88 to 0.80) for rosuvastatin compared with placebo, and -1.43 (95% CI -3.37 to 0.50) for combination therapy vs double placebo. No significant differences were found for other measures.ConclusionsLong-term blood pressure lowering with candesartan plus hydrochlorothiazide, rosuvastatin, or their combination did not significantly affect cognitive decline in older people.ClinicalTrials.gov identifierNCT00468923.Classification of evidenceThis study provides Class II evidence that for older people, candesartan plus hydrochlorothiazide, rosuvastatin, or their combination does not significantly affect cognitive decline.

Original languageEnglish
Pages (from-to)E1435-E1446
JournalNeurology
Volume92
Issue number13
DOIs
Publication statusPublished - 26 Mar 2019

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

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