Evidence map›Paper›PMID 33835214›Full record

ReviewSeminars in immunopathology2021

How will artificial intelligence and bioinformatics change our understanding of IgA Nephropathy in the next decade?

Roman David Bülow, Daniel Dimitrov, Peter Boor, Julio Saez-Rodriguez

Erratum issuedOpen access · hybridAbstract readReview
In one paragraph

Review in Seminars in immunopathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Extending the landscape of omics technologies by pathomics.NPJ systems biology and applications · 2023
    Article
  6. Validation of two IgA nephropathy risk-prediction tools using a cohort with a long follow-up.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2023
    Article
  7. Article
  8. Review
  9. Article
  10. Advances in proteomic profiling of pediatric kidney diseases.Pediatric nephrology (Berlin, Germany) · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. IgA nephropathy: a perspective for 2021.Seminars in immunopathology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Roman David Bülow *University Hospital RWTH Aachen, Institute of Pathology, Aachen, Germany.ORCID 0000-0002-8527-7353
Daniel Dimitrov *Faculty of Medicine, Heidelberg University, Heidelberg, Germany.ORCID 0000-0002-5197-2112
Peter BoorUniversity Hospital RWTH Aachen, Institute of Pathology, Aachen, Germany. pboor@ukaachen.de.ORCID 0000-0001-9921-4284
Julio Saez-RodriguezFaculty of Medicine, Heidelberg University, Heidelberg, Germany. julio.saez@uni-heidelberg.de.ORCID 0000-0002-8552-8976
Heidelberg University · DERWTH Aachen University · DEUniversitätsklinikum Aachen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgA nephropathy (IgAN) is the most common glomerulonephritis. It is characterized by the deposition of immune complexes containing immunoglobulin A (IgA) in the kidney's glomeruli, triggering an inflammatory process. In many patients, the disease has a progressive course, eventually leading to end-stage kidney disease. The current understanding of IgAN's pathophysiology is incomplete, with the involvement of several potential players, including the mucosal immune system, the complement system, and the microbiome. Dissecting this complex pathophysiology requires an integrated analysis across molecular, cellular, and organ scales. Such data can be obtained by employing emerging technologies, including single-cell sequencing, next-generation sequencing, proteomics, and complex imaging approaches. These techniques generate complex "big data," requiring advanced computational methods for their analyses and interpretation. Here, we introduce such methods, focusing on the broad areas of bioinformatics and artificial intelligence and discuss how they can advance our understanding of IgAN and ultimately improve patient care. The close integration of advanced experimental and computational technologies with medical and clinical expertise is essential to improve our understanding of human diseases. We argue that IgAN is a paradigmatic disease to demonstrate the value of such a multidisciplinary approach.

Indexed as

Glomerulonephritis, IGAAntigen-Antibody ComplexArtificial IntelligenceComputational BiologyHumansImmunoglobulin AAntigen-Antibody ComplexImmunoglobulin AArtificial intelligenceBioinformaticsIgA nephropathyImagingOmics

Identifiers

PMID33835214
PMCPMC8551101
OpenAlexW3151941374

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.