Evidence map›Paper›PMID 30814647›Full record

Trial reportScientific reports2019

A ferroptosis-based panel of prognostic biomarkers for Amyotrophic Lateral Sclerosis.

David Devos, Caroline Moreau, Maeva Kyheng, Guillaume Garçon, Anne Sophie Rolland, Hélène Blasco, Patrick Gelé, T Timothée Lenglet, C Veyrat-Durebex, Philippe Corcia and 10 more

Erratum issued Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase III
In one paragraph

Trial report in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT02880033 (Modulation of Oxidative Stress and Apoptosis of Energy Metabolism by Deferiprone From the Circulating Lymphocytes of Patients With Parkinson's Disease or Amyotrophic Lateral Sclerosis), which is not on this map. Cited by 80 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 2 pooled it
12.7field-weighted citation impact, top 1% 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.

NCT02880033 nacompletednot on this map

Modulation of Oxidative Stress and Apoptosis of Energy Metabolism by Deferiprone From the Circulating Lymphocytes of Patients With Parkinson's Disease or Amyotrophic Lateral Sclerosis

TypeinterventionalSponsorUniversity Hospital, LilleRan2011 to 2020Enrolled90ConditionsParkinson's Disease, Amyotrophic Lateral Sclerosis, Oxidative Stress, Iron OverloadArmsdeferiprone, placebo
3 · Its place in the literature

Who cites it

80 citing papers in PubMed, 2 syntheses or guidelines pooled it, 133 citations in OpenAlex.

  1. Pooled it
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  10. Neuroferroptosis in health and diseases.Nature reviews. Neuroscience · 2025
    Review
  11. Ferroptosis: a new target for depression prevention and treatment.Journal of neural transmission (Vienna, Austria : 1996) · 2025
    Review
  12. Review
  13. New developments in imaging in ALS.Journal of neurology · 2025
    Review
  14. Review
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20 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 9 institutions in 5 countries.

David DevosDepartment of Neurology, ALS Center, Lille University, INSERM UMRS_1171, University Hospital Center, LICEND COEN Center, Lille, France. david.devos@chru-lille.fr.ORCID 0000-0002-2417-799X
Caroline MoreauDepartment of Neurology, ALS Center, Lille University, INSERM UMRS_1171, University Hospital Center, LICEND COEN Center, Lille, France.
Maeva KyhengDepartment of Biostatistics, Lille University, University Hospital Center, Lille, France.
Guillaume GarçonUniv. Lille, CHU Lille, Institut Pasteur de Lille, EA4483 IMPECS-IMPact de l'Environnement Chimique sur la Santé humaine, Lille, France.
Anne Sophie RollandDepartment of Medical Pharmacology, Lille University, INSERM UMRS_1171, University Hospital Center, LICEND COEN Center, Lille, France.
Hélène BlascoUniversité François-Rabelais, Inserm U930, Laboratoire de Biochimie, CHRU de Tours, France.
Patrick GeléCRB/CIC1403, Université de LILLE, Lille, France.
T Timothée LengletAPHP, Department of Neurophysiology, Pitié-Salpêtrière Hospital, Paris, France.
C Veyrat-DurebexUniversité François-Rabelais, Inserm U930, Laboratoire de Biochimie, CHRU de Tours, France.
Philippe CorciaCentre Constitutif SLA, Tours-Fédération des centres SLA Tours-Limoges, LITORALS, Tours, France.
Mary DutheilDepartment of Medical Pharmacology, Lille University, INSERM UMRS_1171, University Hospital Center, LICEND COEN Center, Lille, France.
Peter BedeBiomedical Imaging Laboratory, CNRS, INSERM, Sorbonne University, Paris, France.
Andreas JerominQuanterix, Lexington, Massachusetts, USA.
Patrick OecklDepartment of Neurology, Ulm University Hospital, Oberer Eselsberg 45, 89081 Ulm, Ulm, Germany.
Markus OttoDepartment of Neurology, Ulm University Hospital, Oberer Eselsberg 45, 89081 Ulm, Ulm, Germany.ORCID 0000-0003-4273-4267
Vincent MeiningerAPHP, Department of Neurology, Paris ALS Center, Pitié Salpêtrière Hospital, Paris, France.
Véronique Danel-BrunaudDepartment of Neurology, ALS Center, Lille University, INSERM UMRS_1171, University Hospital Center, LICEND COEN Center, Lille, France.
Jean-Christophe DevedjianDepartment of Medical Pharmacology, Lille University, INSERM UMRS_1171, University Hospital Center, LICEND COEN Center, Lille, France.
James A DuceALBORADA Drug Discovery Institute, University of Cambridge, Cambridge Biomedical Campus, Hills Road, Cambridge, CB2 0AH, UK.
Pierre François PradatBiomedical Imaging Laboratory, CNRS, INSERM, Sorbonne University, Paris, France.
Inserm · FRUniversité de Lille · FRUniversité de Tours · FRCentre National de la Recherche Scientifique · FRSorbonne Université · FRQuanterix (United States) · USUniversität Ulm · DEUniversity Hospital Ulm · DEUniversity of Leeds · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accurate patient stratification into prognostic categories and targeting Amyotrophic Lateral Sclerosis (ALS)-associated pathways may pave the way for promising trials. We evaluated blood-based prognostic indicators using an array of pathological markers. Plasma samples were collected as part of a large, phase III clinical trial (Mitotarget/TRO19622) at months 1, 6, 12 and 18. The ALSFRS-r score was used as a proxy of disease progression to assess the predictive value of candidate biological indicators. First, established clinical predictors were evaluated in all 512 patients. Subsequently, pathologic markers, such as proxies of neuronal integrity (Neurofilament light chain and phosphorylated heavy chain), DNA oxidation (8-oxo-2'-desoxyguanosine), lipid peroxidation (4-hydroxy-2-nonenal, isoprostane), inflammation (interleukin-6) and iron status (ferritin, hepcidin, transferrin) were assessed in a subset of 109 patients that represented the whole cohort. Markers of neuronal integrity, DNA and lipid oxidation, as well as iron status at baseline are accurate predictors of disability at 18-month follow-up. The composite scores of these markers in association with established clinical predictors enable the accurate forecasting of functional decline. The identified four biomarkers are all closely associated with 'ferroptosis', a recently discovered form of programmed cell death with promising therapeutic targets. The predictive potential of these pathophysiology-based indicators may offer superior patient stratification for future trials, individualised patient care and resource allocation.

Indexed as

8-Hydroxy-2'-DeoxyguanosineAdultAldehydesAmyotrophic Lateral SclerosisBiomarkersDisease ProgressionFemaleFerritinsFerroptosisFollow-Up StudiesHumansIronIsoprostanesLipid PeroxidationMaleMiddle Aged4-hydroxy-2-nonenal8-Hydroxy-2'-DeoxyguanosineAldehydesBiomarkersFerritinsIronIsoprostanesneurofilament protein LNeurofilament Proteins

Identifiers

PMID30814647
PMCPMC6393674
OpenAlexW2919525768

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Registered trials

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.