Evidence map›Paper›PMID 35767852›Full record

ArticleNephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association2023

The role of dendrin in IgA nephropathy.

Anna Levin, Angelina Schwarz, Jenny Hulkko, Liqun He, Ying Sun, Peter Barany, Annette Bruchfeld, Maria Herthelius, Lars Wennberg, Kerstin Ebefors and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 1 country.

Anna LevinDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-1299-6920
Angelina SchwarzDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.
Jenny HulkkoDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.
Liqun HeDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Ying SunDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Peter BaranyDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.
Annette BruchfeldDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-9752-9941
Maria HertheliusDepartment of Clinical Science, Intervention, and Technology, Division of Pediatrics, Karolinska Institutet, Stockholm, Sweden.
Lars WennbergDepartment of Clinical Science, Intervention and Technology, Division of Transplantation Surgery, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden.
Kerstin EbeforsDepartment of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Jaakko PatrakkaDepartment of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Christer BetsholtzDepartment of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Jenny NyströmDepartment of Physiology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Johan MölneDepartment of Laboratory Medicine, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Kjell HultenbyDepartment of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.
Anna WitaspDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.
Annika WernersonDepartment of Clinical Science, Intervention and Technology, Divison of Renal Medicine, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEUniversity of Gothenburg · SEUppsala University · SEKarolinska University Hospital · SELinköping University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmunoglobulin A nephropathy (IgAN) and its systemic variant IgA vasculitis (IgAV) damage the glomeruli, resulting in proteinuria, hematuria and kidney impairment. Dendrin is a podocyte-specific protein suggested to be involved in the pathogenesis of IgAN. Upon cell injury, dendrin translocates from the slit diaphragm to the nucleus, where it is suggested to induce apoptosis and cytoskeletal changes, resulting in proteinuria and accelerated disease progression in mice. Here we investigated gene and protein expression of dendrin in relation to clinical and histopathological findings to further elucidate its role in IgAN/IgAV.

methodsGlomerular gene expression was measured using microarray on 30 IgAN/IgAV patients, 5 patients with membranous nephropathy (MN) and 20 deceased kidney donors. Dendrin was spatially evaluated on kidney tissue sections by immunofluorescence (IF) staining (IgAN patients, n = 4; nephrectomized kidneys, n = 3) and semi-quantified by immunogold electron microscopy (IgAN/IgAV patients, n = 21; MN, n = 5; living kidney donors, n = 6). Histopathological grading was performed according to the Oxford and Banff classifications. Clinical data were collected at the time of biopsy and follow-up.

resultsDendrin mRNA levels were higher (P = .01) in IgAN patients compared with MN patients and controls and most prominently in patients with preserved kidney function and fewer chronic histopathological changes. Whereas IF staining did not differ between groups, immunoelectron microscopy revealed that a higher relative nuclear dendrin concentration in IgAN patients was associated with a slower annual progression rate and milder histopathological changes.

conclusionDendrin messenger RNA levels and relative nuclear protein concentrations are increased and associated with a more benign phenotype and progression in IgAN/IgAV patients.

Indexed as

Glomerulonephritis, IGAGlomerulonephritis, MembranousIgA VasculitisAnimalsKidney GlomerulusMiceNerve Tissue ProteinsProteinuriadendrinNerve Tissue Proteinschronic kidney diseasedendrinIgA nephropathyimmunoelectron microscopymicroarray

Identifiers

PMID35767852
PMCPMC9923709
OpenAlexW4283758681

What OpenQuestion holds

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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.