Evidence map›Paper›PMID 28473934›Full record

ArticleCase reports in nephrology2017

In Acute IgA Nephropathy, Proteinuria and Creatinine Are in the Spot, but Podocyturia Operates in Silence: Any Place for Amiloride?

H Trimarchi, M Paulero, R Canzonieri, A Schiel, A Iotti, C Costales-Collaguazo, A Stern, M Forrester, F Lombi, V Pomeranz and 5 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in nephrology, 2017. 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
0.7field-weighted citation impact, top 31% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. The Perspective of Vitamin D on suPAR-Related AKI in COVID-19.International journal of molecular sciences · 2022
    Review
  4. Review
  5. Review
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

15 authors at 2 institutions in 1 country.

H TrimarchiNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0002-6921-4811
M PauleroNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
R CanzonieriBiochemistry, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0003-1876-137X
A SchielBiochemistry, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0001-7837-7156
A IottiPathology Services, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
C Costales-CollaguazoIFIBIO Houssay-UBA CONICET, Facultad de Medicina, Universidad de Buenos Aires, Argentina.
A SternBiochemistry, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
M ForresterNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
F LombiNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
V PomeranzNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
R IriarteNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
T RengelNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
I Gonzalez-HoyosNephrology, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.
A MuryanBiochemistry, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0002-9144-4699
E ZottaPathology Services, Hospital Británico de Buenos Aires, Buenos Aires, Argentina.ORCID 0000-0001-6314-5264
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

IgA nephropathy is the most frequent cause of primary glomerulonephritis, portends erratic patterns of clinical presentation, and lacks specific treatment. In general, it slowly progresses to end-stage renal disease. The clinical course and the response to therapy are usually assessed with proteinuria and serum creatinine. Validated biomarkers have not been identified yet. In this report, we present a case of acute renal injury with proteinuria and microscopic hematuria in a young male. A kidney biopsy disclosed IgA nephropathy. Podocyturia was significantly elevated compared to normal subjects. Proteinuria, renal function, and podocyturia improved promptly after steroids and these variables remained normal after one year of follow-up, when steroids had already been discontinued and patient continued on valsartan and amiloride. Our report demonstrates that podocyturia is critically elevated during an acute episode of IgA nephropathy, and its occurrence may explain the grim long-term prognosis of this entity. Whether podocyturia could be employed in IgA nephropathy as a trustable biomarker for treatment assessment or even for early diagnosis of IgA nephropathy relapses should be further investigated.

Identifiers

PMID28473934
PMCPMC5394405
OpenAlexW2604549558

What OpenQuestion holds

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LicenceCC BY
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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.