Evidence map›Paper›PMID 31838587›Full record

ArticleVirchows Archiv : an international journal of pathology2020

Matrix-assisted laser desorption/ionization mass spectrometry imaging to uncover protein alterations associated with the progression of IgA nephropathy.

Mariia Ivanova, Olena Dyadyk, Dmytro Ivanov, Francesca Clerici, Andrew Smith, Fulvio Magni

Abstract read
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In one paragraph

Article in Virchows Archiv : an international journal of pathology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Non-invasive molecular imaging of kidney diseases.Nature reviews. Nephrology · 2021
    Review
  5. Article
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

6 authors.

Mariia IvanovaDepartment of Medicine and Surgery, Clinical Proteomics and Metabolomics Unit, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, Italy. mesangium88@gmail.com.ORCID http://orcid.org/0000-0002-7636-1000
Olena DyadykP.L. Shupyk National Medical Academy of Postgraduate Education (NMAPE), Kiev, Ukraine.ORCID http://orcid.org/0000-0002-9912-4286
Dmytro IvanovP.L. Shupyk National Medical Academy of Postgraduate Education (NMAPE), Kiev, Ukraine.ORCID http://orcid.org/0000-0003-2609-0051
Francesca ClericiDepartment of Medicine and Surgery, Clinical Proteomics and Metabolomics Unit, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, Italy.
Andrew SmithDepartment of Medicine and Surgery, Clinical Proteomics and Metabolomics Unit, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, Italy.ORCID http://orcid.org/0000-0001-6530-6113
Fulvio MagniDepartment of Medicine and Surgery, Clinical Proteomics and Metabolomics Unit, University of Milano-Bicocca, Via Raoul Follereau 3, 20854, Vedano al Lambro, Italy.ORCID http://orcid.org/0000-0002-8663-0374

Funding

FIRB RBRN07BMCT_11
6 · The paper itself

Abstract

IgA nephropathy (IgAN) is one of the most diffuse glomerulonephrites worldwide, and many issues still remain regarding our understanding of its pathogenesis. The disease is diagnosed by renal biopsy examination, but potential pitfalls still persist with regard to discriminating its primary origin and, as a result, determining patient outcome remains challenging. In this pilot study, matrix-assisted laser desorption/ionization (MALDI) mass spectrometry imaging (MSI) was performed on renal biopsies obtained from patients with IgAN (n = 11) and other mesangioproliferative glomerulonephrites (MesPGN, n = 6) in order to enlighten proteomic alterations that may be associated with the progression of IgAN. Differences in the proteomic profiles of IgAN and MesPGN tissue could clearly be detected using this approach and, furthermore, 14 signals (AUC ≥ 0.8) were observed to have an altered intensity among the different CKD stages within the IgAN group. In particular, large increases in the intensity of these signals could be observed at CKD stages II and above. These signals primarily corresponded to proteins involved in either inflammatory and healing pathways and their increased intensity was localized within regions of tissue with large amounts of inflammatory cells or sclerosis. Despite much work in recent years, our molecular understanding of IgAN progression remains incomplete. This pilot study represents a promising starting point in the search for novel protein markers that can assist clinicians in better understanding the pathogenesis of IgAN and highlighting those patients who may progress to end-stage renal disease.

Indexed as

Spectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAdolescentAdultBiomarkersChildChild, PreschoolDisease ProgressionFemaleGlomerulonephritis, IGAHumansImmunochemistryKidneyMalePilot ProjectsProteomicsUkraineBiomarkersVimentinVIM protein, humanChronic kidney diseaseIgA nephropathyMALDI-MSIMass spectrometryMesangioproliferative glomerulonephritisProteomics

Identifiers

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Registered trials

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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.