Evidence map›Paper›PMID 38668984›Full record

ArticleJournal of nephrology2024

X-linked Alport syndrome presenting in mother and son with the same unique histopathological features.

Nicolas A D Bergeron, Alexandre P Garneau, Mathieu Rousseau-Gagnon, Julie Riopel, Paul Isenring

Abstract readCase Reports
In one paragraph

Article in Journal of nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. An Alport variant illuminates the bioactivity of the collagen IVbioRxiv : the preprint server for biology · 2026
    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

5 authors.

Nicolas A D BergeronService of Nephrology, L'Hôtel-Dieu de Québec Research Center, CHU de Québec-Université Laval, 10 McMahon Street (Room 3852), Québec, QC, G1R 2J6, Canada.
Alexandre P GarneauService de Néphrologie-Transplantation Rénale Adultes, Hôpital Necker-Enfants Malades, AP-HP, Inserm U1151, Université Paris Cité, Rue de Sèvres, Paris, France.
Mathieu Rousseau-GagnonService of Nephrology, L'Hôtel-Dieu de Québec Research Center, CHU de Québec-Université Laval, 10 McMahon Street (Room 3852), Québec, QC, G1R 2J6, Canada.
Julie RiopelService of Pathology, CHU de Québec-Université Laval, Québec, QC, G1R 2J6, Canada.
Paul IsenringService of Nephrology, L'Hôtel-Dieu de Québec Research Center, CHU de Québec-Université Laval, 10 McMahon Street (Room 3852), Québec, QC, G1R 2J6, Canada. paul.isenring@crhdq.ulaval.ca.ORCID 0000-0002-5569-6258

Funding

Canadian Institutes of Health and Research Grant ProjectKidney Foundation of Canada Biomedical Research
6 · The paper itself

Abstract

Alport syndrome has been linked to three different genes, that is, COL4A3, COL4A4 and COL4A5. It is characterized by progressive and non-specific glomerulosclerosis with irregular thickening of the glomerular basement membrane (GBM). At times, the histopathologic picture is dominated by lesions that are consistent with focal and segmental glomerulosclerosis or IgA nephropathy. Here, we report the cases of two related individuals (mother and son) who were diagnosed with COL4A5-related Alport syndrome due to a missense variant (p.Gly1170Ser) in a G-X-Y repeat and found to present the same highly unusual histopathological abnormalities on their kidney biopsies. One of the abnormalities shared, which does not appear to have been reported, was reduced COL4A5 immunolabeling that was limited to Bowman's capsule even though the ultrastructure of the GBM was distorted. The other abnormality was superimposed segmental IgA deposition in both individuals, accompanied by mesangial changes in the mother. We feel that these findings provide novel insight into the mechanisms of disease manifestation in Alport syndrome. They suggest, in particular, that collagen expression and/or assemblies in Bowman's capsule is more vulnerable to missense mutations in COL4A5 than elsewhere in the kidney. Our findings also suggest that certain coinherited gene polymorphisms act as unexpectedly important phenotypic determinants in COL4A-related disorders.

Indexed as

Collagen Type IVGlomerular Basement MembraneMutation, MissenseNephritis, HereditaryAdultBiopsyBowman CapsuleGenetic Predisposition to DiseaseHumansImmunoglobulin AMiddle AgedPedigreePhenotypeCOL4A5 protein, humanCollagen Type IVImmunoglobulin AAlport syndromeBowman’s capsuleCOL4A5Collagen assemblyIgA nephropathy

Identifiers

PMID38668984
PMCPMC11150303

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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.