Evidence map›Paper›PMID 20681980›Full record

ReviewInternational journal of experimental pathology2011

Congenital ureteropelvic junction obstruction: human disease and animal models.

Julie Klein, Julien Gonzalez, Mathieu Miravete, Cécile Caubet, Rana Chaaya, Stéphane Decramer, Flavio Bandin, Jean-Loup Bascands, Bénédicte Buffin-Meyer, Joost P Schanstra

Open access · bronzeAbstract readReview
In one paragraph

Review in International journal of experimental pathology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 21% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 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

10 authors at 3 institutions in 1 country.

Julie KleinInstitut National de la Santé et de la Recherche Médicale (INSERM), Toulouse, France.
Julien Gonzalez
Mathieu Miravete
Cécile Caubet
Rana Chaaya
Stéphane Decramer
Flavio Bandin
Jean-Loup Bascands
Bénédicte Buffin-Meyer
Joost P Schanstra
Université Toulouse III - Paul Sabatier · FRInserm · FRHôpital des Enfants · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ureteropelvic junction (UPJ) obstruction is the most frequently observed cause of obstructive nephropathy in children. Neonatal and foetal animal models have been developed that mimic closely what is observed in human disease. The purpose of this review is to discuss how obstructive nephropathy alters kidney histology and function and describe the molecular mechanisms involved in the progression of the lesions, including inflammation, proliferation/apoptosis, renin-angiotensin system activation and fibrosis, based on both human and animal data. Also we propose that during obstructive nephropathy, hydrodynamic modifications are early inducers of the tubular lesions, which are potentially at the origin of the pathology. Finally, an important observation in animal models is that relief of obstruction during kidney development has important effects on renal function later in adult life. A major short-coming is the absence of data on the impact of UPJ obstruction on long-term adult renal function to elucidate whether these animal data are also valid in humans.

Indexed as

AnimalsApoptosisCell ProliferationDisease Models, AnimalDisease ProgressionHumansHydrodynamicsKidneyMiceRabbitsRatsRenin-Angiotensin SystemSwineUreteral Obstruction

Identifiers

PMID20681980
PMCPMC3101490
OpenAlexW1922006896

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.