Evidence map›Paper›PMID 25853334›Full record

ArticleKidney international2015

Common histological patterns in glomerular epithelial cells in secondary focal segmental glomerulosclerosis.

Christoph Kuppe, Hermann-Josef Gröne, Tammo Ostendorf, Toin H van Kuppevelt, Peter Boor, Jürgen Floege, Bart Smeets, Marcus J Moeller

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Kidney international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 71 citations in OpenAlex.

  1. Cell-cell crosstalk in kidney health and disease.Nature reviews. Nephrology · 2026
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  8. Targeting tissue-resident memory CD8Molecular therapy : the journal of the American Society of Gene Therapy · 2022
    Article
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  10. The Pathology Lesion Patterns of Podocytopathies: How and why?Frontiers in cell and developmental biology · 2022
    Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Steroid therapy in children with IgA nephropathy.Pediatric nephrology (Berlin, Germany) · 2020
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Christoph KuppeDepartment of Internal Medicine II, Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany.
Hermann-Josef GröneDepartment of Cellular and Molecular Pathology, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Tammo OstendorfDepartment of Internal Medicine II, Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany.
Toin H van KuppeveltDepartment of Biochemistry, Radboud University Medical Centre, Nijmegen, The Netherlands.
Peter BoorDepartment of Pathology, RWTH Aachen University Hospital, Aachen, Germany.
Jürgen FloegeDepartment of Internal Medicine II, Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany.
Bart SmeetsDepartment of Internal Medicine II, Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany.
Marcus J MoellerDepartment of Internal Medicine II, Nephrology and Clinical Immunology, RWTH Aachen University Hospital, Aachen, Germany.
Universitätsklinikum Aachen · DERadboud University Nijmegen · NLGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parietal epithelial cells (PECs) are involved in the development of sclerotic lesions in primary focal and segmental glomerulosclerosis (FSGS). Here, the role of PECs was explored in the more common secondary FSGS lesions in 68 patient biopsies, diagnosed with 11 different frequently or rarely encountered glomerular pathologies and additional secondary FSGS lesions. For each biopsy, one section was quadruple stained for PECs (ANXA3), podocytes (synaptopodin), PEC matrix (LKIV69), and Hoechst (nuclei), and a second was quadruple stained for activated PECs (CD44 and cytokeratin-19), PEC matrix, and nuclei. In all lesions, cellular adhesions (synechiae) between Bowman's capsule and the tuft were formed by cells expressing podocyte and/or PEC markers. Cells expressing PEC markers were detected in all FSGS lesions independent of the underlying glomerular disease and often stained positive for markers of activation. Small FSGS lesions, which were hardly identified on PAS sections previously, were detectable by immunofluorescent staining using PEC markers, potentially improving the diagnostic sensitivity to identify these lesions. Thus, similar patterns of cells expressing podocyte and/or PEC markers were found in the formation of secondary FSGS lesions independent of the underlying glomerular disease. Hence, our findings support the hypothesis that FSGS lesions follow a final cellular pathway to nephron loss that includes involvement of cells expressing PEC markers.

Indexed as

AdultAgedAnnexin A3Bowman CapsuleCell AdhesionCell NucleusClaudin-1Epithelial CellsFemaleFluorescent Antibody TechniqueGlomerulosclerosis, Focal SegmentalHumansHyaluronan ReceptorsKeratin-19Kidney GlomerulusMaleAnnexin A3Claudin-1Hyaluronan ReceptorsKeratin-19Microfilament ProteinsSYNPO protein, human

Identifiers

PMID25853334
OpenAlexW2036638439

What OpenQuestion holds

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Read underepoch 390

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.