Evidence map›Paper›PMID 30747154›Full record

ArticleClinical kidney journal2019

Early decrease in the podocalyxin to synaptopodin ratio in urinary Fabry podocytes.

Hernán Trimarchi, Romina Canzonieri, Cristian Costales-Collaguazo, Juan Politei, Anibal Stern, Matias Paulero, Ivan González-Hoyos, Amalia Schiel, Tatiana Rengel, Mariano Forrester and 5 more

Open access · goldAbstract read
In one paragraph

Article in Clinical kidney journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Pathology and pathogenic pathways in fabry nephropathy.Clinical and experimental nephrology · 2021
    Review
  7. Article
  8. Renal Manifestations of Fabry Disease: A Narrative Review.Canadian journal of kidney health and disease · 2021
    Review
  9. Fabry disease: where are we now?International urology and nephrology · 2020
    Review
  10. Review
  11. Review
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 2 institutions in 1 country.

Hernán TrimarchiNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0002-6921-4811
Romina CanzonieriCentral Laboratory, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Cristian Costales-CollaguazoIFIBIO Houssay, CONICET, Physiopathology, Pharmacy and Biochemistry Faculty, Universidad de Buenos Aires, Buenos Aires, Argentina.
Juan PoliteiNeurology Department, Laboratorio Neuroquímica Dr Néstor Chamoles Buenos Aires, Buenos Aires, Argentina.
Anibal SternCentral Laboratory, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Matias PauleroNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Ivan González-HoyosNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Amalia SchielCentral Laboratory, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Tatiana RengelNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Mariano ForresterNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Fernando LombiNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Vanesa PomeranzNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Romina IriarteNephrology Service, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Alexis MuryanCentral Laboratory, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
Elsa ZottaIFIBIO Houssay, CONICET, Physiopathology, Pharmacy and Biochemistry Faculty, Universidad de Buenos Aires, Buenos Aires, Argentina.
Hospital Británico de Buenos Aires · ARConsejo Nacional de Investigaciones Científicas y Técnicas · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn Fabry nephropathy, podocyturia is an early event that may lead to glomerulosclerosis and chronic kidney disease. The glycocalyx is a potential podocyte damaged compartment in glomerulopathies. We investigated glycocalyx podocalyxin in urinary detached podocytes compared with cytoplasmic synaptopodin.

methodsThis was a cross-sectional study including 68 individuals: Controls (

resultsFabry patients displayed higher podocyturia than controls. Fabry treated subjects (

conclusionFabry patients present higher podocyturia and a presumably more damaged glycocalyx assessed by podocalyxin. Treated patients had significant higher proteinuria suggesting ERT is initiated late, at advanced stages. The degree of podocalyxin-negative podocytes was similar in both groups, but colocalization was associated with lower proteinuria. Podocyturia assessed by podocalyxin alone may be underestimated. The implications of podocyte glycocalyx damage deserve further investigations.

Indexed as

Fabry nephropathypodocalyxinpodocytepodocyturiasynaptopodin

Identifiers

PMID30747154
PMCPMC6366138
OpenAlexW2884013746

What OpenQuestion holds

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LicenceCC BY-NC
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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.