Evidence map›Paper›PMID 38551218›Full record

Trial reportHealth technology assessment (Winchester, England)2024

Allopurinol and cardiovascular outcomes in patients with ischaemic heart disease: the ALL-HEART RCT and economic evaluation.

Isla S Mackenzie, Christopher J Hawkey, Ian Ford, Nicola Greenlaw, Filippo Pigazzani, Amy Rogers, Allan D Struthers, Alan G Begg, Li Wei, Anthony J Avery and 10 more

Open access · diamondAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Health technology assessment (Winchester, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Uric acid and subclinical atherosclerosis: distinct associations across coronary and carotid arteries.Clinical research in cardiology : official journal of the German Cardiac Society · 2026
    Article
  3. Mechanism and use strategy of uric acid-lowering drugs on coronary heart disease.International journal of cardiology. Heart & vasculature · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 6 institutions in 1 country.

Isla S MackenzieMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-3680-7127
Christopher J HawkeyNottingham Digestive Diseases Centre, University of Nottingham, Nottingham, UK.ORCID 0000-0002-6031-1017
Ian FordThe Robertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.ORCID 0000-0001-5927-1823
Nicola GreenlawThe Robertson Centre for Biostatistics, University of Glasgow, Glasgow, UK.ORCID 0000-0003-3847-1126
Filippo PigazzaniMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-8726-306X
Amy RogersMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0001-5207-7032
Allan D StruthersMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-2926-2528
Alan G BeggMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-9712-9227
Li WeiSchool of Pharmacy, University College London, London, UK.ORCID 0000-0001-8840-7267
Anthony J AveryCentre for Academic Primary Care, School of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0001-7591-4438
Jaspal S TaggarCentre for Academic Primary Care, School of Medicine, University of Nottingham, Nottingham, UK.ORCID 0000-0002-5031-0977
Andrew WalkerSalus Alba, Glasgow, UK.ORCID 0000-0002-5372-856X
Suzanne L DuceMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0001-6539-1311
Rebecca J BarrMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0003-4820-4240
Jennifer S DumbletonNottingham Digestive Diseases Centre, University of Nottingham, Nottingham, UK.ORCID 0000-0001-9099-5555
Evelien D RookeMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0002-9174-777X
Jonathan N TownendInstitute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK.ORCID 0000-0002-5881-5806
Lewis D RitchieAcademic Primary Care, University of Aberdeen, Aberdeen, UK.ORCID 0000-0002-9380-7641
Thomas M MacDonaldMEMO Research, Division of Molecular and Clinical Medicine, University of Dundee, Dundee, UK.ORCID 0000-0001-5189-6669
ALL-HEART Study Group
University of Dundee · GBUniversity of Nottingham · GBUniversity of Glasgow · GBUniversity College London · GBUniversity of Aberdeen · GBUniversity of Birmingham · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Allopurinol is a xanthine oxidase inhibitor that lowers serum uric acid and is used to prevent acute gout flares in patients with gout. Observational and small interventional studies have suggested beneficial cardiovascular effects of allopurinol. Objective: To determine whether allopurinol improves major cardiovascular outcomes in patients with ischaemic heart disease. Design: Prospective, randomised, open-label, blinded endpoint multicentre clinical trial. Setting: Four hundred and twenty-four UK primary care practices. Participants: Aged 60 years and over with ischaemic heart disease but no gout. Interventions: Participants were randomised (1 : 1) using a central web-based randomisation system to receive allopurinol up to 600 mg daily that was added to usual care or to continue usual care. Main outcome measures: The primary outcome was the composite of non-fatal myocardial infarction, non-fatal stroke or cardiovascular death. Secondary outcomes were non-fatal myocardial infarction, non-fatal stroke, cardiovascular death, all-cause mortality, hospitalisation for heart failure, hospitalisation for acute coronary syndrome, coronary revascularisation, hospitalisation for acute coronary syndrome or coronary revascularisation, all cardiovascular hospitalisations, quality of life and cost-effectiveness. The hazard ratio (allopurinol vs. usual care) in a Cox proportional hazards model was assessed for superiority in a modified intention-to-treat analysis. Results: From 7 February 2014 to 2 October 2017, 5937 participants were enrolled and randomised to the allopurinol arm ( Limitations: The results may not be generalisable to younger populations, other ethnic groups or patients with more acute ischaemic heart disease. One thousand six hundred and thirty-seven participants (57.4%) in the allopurinol arm withdrew from randomised treatment, but an on-treatment analysis gave similar results to the main analysis. Conclusions: The ALL-HEART study showed that treatment with allopurinol 600 mg daily did not improve cardiovascular outcomes compared to usual care in patients with ischaemic heart disease. We conclude that allopurinol should not be recommended for the secondary prevention of cardiovascular events in patients with ischaemic heart disease but no gout. Future work: The effects of allopurinol on cardiovascular outcomes in patients with ischaemic heart disease and co-existing hyperuricaemia or clinical gout could be explored in future studies. Trial registration: This trial is registered as EU Clinical Trials Register (EudraCT 2013-003559-39) and ISRCTN (ISRCTN 32017426). Funding: This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR award ref: 11/36/41) and is published in full in

Indexed as

Acute Coronary SyndromeGoutMyocardial InfarctionMyocardial IschemiaStrokeAgedAllopurinolCost-Benefit AnalysisFemaleHumansMaleMiddle AgedProspective StudiesQuality of LifeUric AcidAllopurinolUric AcidALLOPURINOLCARDIOVASCULAR SYSTEMCAUSE OF DEATHCOST-BENEFIT ANALYSISGOUTHUMANSMULTICENTRE STUDIESMYOCARDIAL INFARCTIONMYOCARDIAL ISCHAEMIAPROSPECTIVE STUDIESRANDOMISED CONTROLLED TRIALSSTROKEUNITED KINGDOMXANTHINE OXIDASE

Identifiers

PMID38551218
PMCPMC11017142
OpenAlexW4393321074

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.