Evidence map›Paper›PMID 35969278›Full record

ArticlePediatric nephrology (Berlin, Germany)2023

Pioglitazone enhances proteinuria reduction in complicated pediatric nephrotic syndrome.

Tracy E Hunley, Guillermo Hidalgo, Kar Hui Ng, Yoko Shirai, Kenichiro Miura, Hostensia M Beng, Qiang Wu, Motoshi Hattori, William E Smoyer

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Article in Pediatric nephrology (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

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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

9 authors at 5 institutions in 3 countries.

Tracy E Hunley *Monroe Carell Jr. Children's Hospital at Vanderbilt, Vanderbilt University School of Medicine, Nashville, TN, USA.
Guillermo Hidalgo *Department of Pediatrics, Brody School of Medicine, East Carolina University, Greenville, NC, USA.
Kar Hui NgDepartment of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Republic of Singapore.
Yoko ShiraiTokyo Women's Medical University, Tokyo, Japan.
Kenichiro MiuraTokyo Women's Medical University, Tokyo, Japan.
Hostensia M BengDepartment of Pediatrics, Brody School of Medicine, East Carolina University, Greenville, NC, USA.
Qiang WuEast Carolina University, Greenville, NC, USA.
Motoshi HattoriTokyo Women's Medical University, Tokyo, Japan.
William E SmoyerCenter for Clinical and Translational Research, Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA. William.Smoyer@Nationwidechildrens.org.
East Carolina University · USTokyo Women's Medical University · JPMonroe Carell Jr. Children's Hospital · USNational University of Singapore · SGNationwide Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNephrotic syndrome (NS) is a common pediatric kidney disease, yet current treatments for complicated NS are only partially effective and have significant toxicity. There is no Food and Drug Administration (FDA)- or European Medicines Agency (EMA)-approved safe and effective treatment for NS. Thiazolidinediones (TZDs) have been shown to reduce proteinuria in both diabetic and non-diabetic kidney disease and in preclinical studies to directly protect podocytes from injury and reduce proteinuria. Here, we report on the potential utility of the addition of the TZD pioglitazone (PIO) to enhance proteinuria reduction in 8 children and young adults with steroid dependent NS and steroid resistant NS.

methodsClinical data were analyzed in comparable time periods before and after the addition of PIO to their medical regimens. Eight NS patients with minimal change NS (n = 2), focal segmental glomerulosclerosis (FSGS) (n = 4), or collapsing FSGS (n = 2) were evaluated.

resultsPrior to PIO initiation, all children and young adults had already received multiple immunosuppressive medications (mean = 3.75). Five of eight patients (63%; "Responders") had notable proteinuria reduction within 1 month of PIO initiation (62% reduction; P = 0.04) and normalization within 6 months (97% reduction; P = 0.04). PIO-related benefits among the responders included notable increases in serum albumin (2.5 to 3.7 g/dl; P = 0.08), dramatic reductions in hospitalizations for IV albumin infusions and diuresis (11 to 0; P < 0.01), and considerable reduction in total immunosuppression (43% reduction; P > 0.1). Importantly, no patients experienced any adverse events attributable to PIO during a total of 136 patient-months of treatment.

conclusionsWhile confirmatory safety and efficacy studies are needed, these findings suggest pioglitazone (a non-immunosuppressive drug) may be useful to enhance proteinuria reduction in some children and young adults with complicated NS. A higher resolution version of the Graphical abstract is available as Supplementary information.

Indexed as

Glomerulosclerosis, Focal SegmentalNephrotic SyndromeChildHumansPioglitazoneProteinuriaSteroidsYoung AdultPioglitazoneSteroidsDrug repurposingFSGSMinimal change nephrotic syndromeNuclear receptorPodocytePPARγSteroid dependent nephrotic syndromeSteroid resistant nephrotic syndromeTZD

Identifiers

PMID35969278
OpenAlexW4291894188

What Socratic 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 Socratic graph.