Evidence map›Paper›PMID 35472008›Full record

Trial reportAmerican journal of hematology2022

Proton pump inhibition for secondary hemochromatosis in hereditary anemia: a phase III placebo-controlled randomized cross-over clinical trial.

Annelies van Vuren, Jean Louis Kerkhoffs, Saskia Schols, Anita Rijneveld, Erfan Nur, Dore Peereboom, Yves Gandon, Paco Welsing, Richard van Wijk, Roger Schutgens and 5 more

Open access · hybridAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in American journal of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Review
  3. Metal Ion Signaling in Biomedicine.Chemical reviews · 2025
    Review
  4. Review
  5. Review
  6. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 9 institutions in 3 countries.

Annelies van VurenCenter for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-4258-3836
Jean Louis KerkhoffsDepartment of Hematology, HagaZiekenhuis, The Hague, The Netherlands.ORCID 0000-0001-5107-047X
Saskia ScholsDepartment of Hematology, Radboud university medical center, Nijmegen, The Netherlands.ORCID 0000-0003-2423-2829
Anita RijneveldDepartment of Hematology, Erasmus Medical Center Cancer Institute, Rotterdam, The Netherlands.
Erfan NurDepartment of Hematology, Amsterdam University Centers, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-7069-930X
Dore PeereboomContactgroep Pyruvaatkinasedeficiëntie, Stichting Zeldzame Bloedziekten, Medemblik, The Netherlands.
Yves GandonDepartment of Radiology, CHU Rennes, University of Rennes, Rennes, France.ORCID 0000-0002-7729-6087
Paco WelsingDivision of Internal Medicine and Dermatology, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0003-2361-2803
Richard van WijkCentral Diagnostic Laboratory - Research, Division of Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-8236-8292
Roger SchutgensCenter for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-2762-6033
Wouter van SolingeCentral Diagnostic Laboratory - Research, Division of Laboratories, Pharmacy and Biomedical Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0003-2867-2581
Joannes MarxUniversity Medical Center Utrecht, Utrecht, The Netherlands.
Tim LeinerDepartment of Radiology, Mayo Clinic, Rochester, Minnesota, USA.ORCID 0000-0003-1885-5499
Bart BiemondDepartment of Hematology, Amsterdam University Centers, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-3199-7718
Eduard van BeersCenter for Benign Haematology, Thrombosis and Haemostasis, Van Creveldkliniek, University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-3934-7189
Utrecht University · NLAmsterdam University Medical Centers · NLErasmus MC Cancer Institute · NLHaga Hospital · NLMayo Clinic · USRadboud University Nijmegen · NLSanquin · NLUniversité Rennes 2 · FRUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Iron overload is a severe general complication of hereditary anemias. Treatment with iron chelators is hampered by important side-effects, high costs, and the lack of availability in many countries with a high prevalence of hereditary anemias. In this phase III randomized placebo-controlled trial, we assigned adults with non-transfusion-dependent hereditary anemias with mild-to-moderate iron overload to receive esomeprazole (at a dose of 40 mg twice daily) or placebo for 12 months in a cross-over design. The primary end point was change of liver iron content measured by MRI. A total of 30 participants were enrolled in the trial. Treatment with esomeprazole resulted in a statistically significant reduction in liver iron content that was 0.55 mg Fe/g dw larger than after treatment with placebo (95%CI [0.05 to 1.06]; p = 0.03). Median baseline liver iron content at the start of esomeprazole was 4.99 versus 4.49 mg Fe/g dw at start of placebo. Mean delta liver iron content after esomeprazole treatment was -0.57 (SD 1.20) versus -0.11 mg Fe/g dw (SD 0.75) after placebo treatment. Esomeprazole was well tolerated, reported adverse events were mild and none of the patients withdrew from the study due to side effects. In summary, esomeprazole resulted in a significant reduction in liver iron content when compared to placebo in a heterogeneous group of patients with non-transfusion-dependent hereditary anemias. From an international perspective this result can have major implications given the fact that proton pump inhibitors may frequently be the only realistic therapy for many patients without access to or not tolerating iron chelators.

Indexed as

AnemiaHemochromatosisIron OverloadAdultCross-Over StudiesDouble-Blind MethodEsomeprazoleHumansIronIron Chelating AgentsProton PumpsTreatment OutcomeEsomeprazoleIronIron Chelating AgentsProton Pumps

Identifiers

PMID35472008
PMCPMC9325377
OpenAlexW4224482809

What OpenQuestion holds

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LicenceCC BY-NC
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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.