Evidence map›Paper›PMID 36869085›Full record

ArticleNature communications2023

Tandem mass tag-based quantitative proteomic profiling identifies candidate serum biomarkers of drug-induced liver injury in humans.

Kodihalli C Ravindra, Vishal S Vaidya, Zhenyu Wang, Joel D Federspiel, Richard Virgen-Slane, Robert A Everley, Jane I Grove, Camilla Stephens, Mireia F Ocana, Mercedes Robles-Díaz and 18 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
9.6field-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.

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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Observational
  13. Review
  14. Article
  15. Methods for causality assessment of idiosyncratic drug-induced liver injury.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Review
  16. Genetic Variants of GBP4: Reduced Risks for Drug-Induced Acute Liver Failure in Non-Finnish European Population.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
  17. Article
  18. Article
  19. Review
  20. Serum/Plasma Proteome in Non-Malignant Liver Disease.International journal of molecular sciences · 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

28 authors at 14 institutions in 7 countries.

Kodihalli C Ravindra *Worldwide Research Development and Medical, Pfizer, USA.
Vishal S Vaidya *Worldwide Research Development and Medical, Pfizer, USA. Vishal.Vaidya@Pfizer.com.
Zhenyu WangWorldwide Research Development and Medical, Pfizer, USA.
Joel D FederspielWorldwide Research Development and Medical, Pfizer, USA.ORCID 0000-0002-2010-0071
Richard Virgen-SlaneWorldwide Research Development and Medical, Pfizer, USA.
Robert A EverleyWorldwide Research Development and Medical, Pfizer, USA.
Jane I GroveNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.ORCID 0000-0002-9950-7201
Camilla StephensServicios de Aparato Digestivo y Farmacología Clínica, Instituto de Investigación Biomédica de Málaga-IBIMA Plataforma Bionand, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Malaga, Spain.ORCID 0000-0002-0796-9610
Mireia F OcanaWorldwide Research Development and Medical, Pfizer, USA.
Mercedes Robles-DíazServicios de Aparato Digestivo y Farmacología Clínica, Instituto de Investigación Biomédica de Málaga-IBIMA Plataforma Bionand, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Malaga, Spain.
M Isabel LucenaServicios de Aparato Digestivo y Farmacología Clínica, Instituto de Investigación Biomédica de Málaga-IBIMA Plataforma Bionand, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Malaga, Spain.ORCID 0000-0001-9586-4896
Raul J AndradeServicios de Aparato Digestivo y Farmacología Clínica, Instituto de Investigación Biomédica de Málaga-IBIMA Plataforma Bionand, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Malaga, Spain.ORCID 0000-0002-1565-0757
Edmond AtallahNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK.ORCID 0000-0002-7341-9174
Alexander L GerbesDepartment of Medicine II, University Hospital, LMU Munich, Munich, Germany.
Sabine WeberDepartment of Medicine II, University Hospital, LMU Munich, Munich, Germany.
Helena Cortez-PintoClínica Universitária de Gastrenterologia, Faculdade de Medicina, Universidade de Lisboa, Lisbon, Portugal.ORCID 0000-0002-8537-8744
Andrew J FowellDepartment of Gastroenterology and Hepatology, Portsmouth Hospitals University NHS Trust, Portsmouth, UK.
Hyder HussainiDepartment of Gastroenterology and Hepatology, Royal Cornwall Hospitals NHS Trust, Cornwall, UK.
Einar S BjornssonDepartment of Gastroenterology, Landspitali University Hospital Reykjavik, Reykjavík, Iceland.
Janisha PatelUniversity Hospital Southampton, Southampton, UK.
Guido StirnimannUniversity Clinic for Visceral Surgery and Medicine, University Hospital Inselspital and University of Bern, Bern, Switzerland.ORCID 0000-0003-3447-264X
Sumita VermaBrighton and Sussex Medical School and University Hospitals Sussex NHS Foundation Trust, Brighton, UK.
Ahmed M ElsharkawyLiver Unit and NIHR Biomedical Research Centre, University Hospitals Birmingham NHS Foundation Trust, Queen Elizabeth Hospital, Birmingham, UK.
William J H GriffithsDepartment of Hepatology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Craig HydeWorldwide Research Development and Medical, Pfizer, USA.ORCID 0000-0002-6939-287X
James W DearPharmacology, Therapeutics and Toxicology, Centre for Cardiovascular Science, University of Edinburgh, The Queen's Medical Research Institute, Edinburgh, UK.ORCID 0000-0002-8630-8625
Guruprasad P AithalNIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK. Guru.Aithal@Nottingham.ac.uk.ORCID 0000-0003-3924-4830
Shashi K RamaiahWorldwide Research Development and Medical, Pfizer, USA. Shashi.Ramaiah@Pfizer.com.
Pfizer (United States) · USCentro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESNottingham University Hospitals NHS Trust · GBLMU Klinikum · DEBrighton and Sussex Medical School · GBCambridge University Hospitals NHS Foundation Trust · GBPortsmouth Hospitals NHS Trust · GBReykjavík University · ISRoyal Cornwall Hospital Trust · GBThe Queen's Medical Research Institute · GBUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Bern · CHUniversity of Lisbon · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diagnosis of drug-induced liver injury (DILI) and its distinction from other liver diseases are significant challenges in drug development and clinical practice. Here, we identify, confirm, and replicate the biomarker performance characteristics of candidate proteins in patients with DILI at onset (DO; n = 133) and follow-up (n = 120), acute non-DILI at onset (NDO; n = 63) and follow-up (n = 42), and healthy volunteers (HV; n = 104). Area under the receiver operating characteristic curve (AUC) for cytoplasmic aconitate hydratase, argininosuccinate synthase, carbamoylphosphate synthase, fumarylacetoacetase, fructose-1,6-bisphosphatase 1 (FBP1) across cohorts achieved near complete separation (range: 0.94-0.99) of DO and HV. In addition, we show that FBP1, alone or in combination with glutathione S-transferase A1 and leukocyte cell-derived chemotaxin 2, could potentially assist in clinical diagnosis by distinguishing NDO from DO (AUC range: 0.65-0.78), but further technical and clinical validation of these candidate biomarkers is needed.

Indexed as

Chemical and Drug Induced Liver InjuryProteomicsArgininosuccinate SynthaseBiomarkersCD8 AntigensFructoseHumansArgininosuccinate SynthaseBiomarkersCD8 AntigensFructose

Identifiers

PMID36869085
PMCPMC9984368
OpenAlexW4323043065

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.