Evidence map›Paper›PMID 27215552›Full record

ArticleMolecular & cellular proteomics : MCP2016

Urinary Proteomics Yield Pathological Insights for Ureteropelvic Junction Obstruction.

John W Froehlich, Stephen A Kostel, Patricia S Cho, Andrew C Briscoe, Hanno Steen, Ali R Vaezzadeh, Richard S Lee

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Article
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  14. Urinary biomarkers for renal tract malformations.Expert review of proteomics · 2016
    Review
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

John W FroehlichFrom the ‡Department of Urology and the Urological Diseases Research Center, §Proteomics Center at Children's Hospital Boston, Boston, MA.
Stephen A KostelFrom the ‡Department of Urology and the Urological Diseases Research Center, §Proteomics Center at Children's Hospital Boston, Boston, MA.
Patricia S ChoFrom the ‡Department of Urology and the Urological Diseases Research Center, §Proteomics Center at Children's Hospital Boston, Boston, MA.
Andrew C BriscoeFrom the ‡Department of Urology and the Urological Diseases Research Center, §Proteomics Center at Children's Hospital Boston, Boston, MA.
Hanno Steen§Proteomics Center at Children's Hospital Boston, Boston, MA ¶Department of Pathology, Children's Hospital Boston and Harvard Medical School, Boston, MA;
Ali R VaezzadehFrom the ‡Department of Urology and the Urological Diseases Research Center, §Proteomics Center at Children's Hospital Boston, Boston, MA.
Richard S LeeFrom the ‡Department of Urology and the Urological Diseases Research Center, §Proteomics Center at Children's Hospital Boston, Boston, MA richard.lee@childrens.harvard.edu.

Funding

Research Training in Pediatric Urology/CHB T32T32DK060442 · NIDDK · CHILDREN'S HOSPITAL BOSTON · PI ADAM, ROSALYN M · 2002 to 2023
$2.5M
Early Validation of Urinary Biomarkers of Renal ObstructionR01DK096238 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI LEE, RICHARD SANG-YONG · 2013 to 2017
$1.3M
NIDDK NIH HHS R01 DK096238NIDDK NIH HHS T32 DK060442
6 · The paper itself

Abstract

Prenatal hydronephrosis is a common condition that may spontaneously resolve after birth. However, this condition can result in renal damage and requires surgical correction in a number of cases. Preventing renal damage is paramount, but existing diagnostic technology is invasive, exposes infants to radiation, is costly, and is often indeterminate. A better understanding of the pathophysiology of renal obstruction as reflected in the urinary proteome may provide new insights into the disease that could potentially alter the clinical management of hydronephrosis. We performed a quantitative proteomics study of urine that was surgically obtained from eight clinically significant, unilaterally obstructed infants versus eight healthy controls, with the goal of identifying quantitatively varying proteins and the biological networks associated with them. Notably, urine was obtained from both the obstructed kidney and the bladder. Over 1100 proteins were identified, and a total of 76 quantitatively varying proteins were identified. Proteins involved in oxidative stress, inflammation, and renal disease pathways showed the most significant abundance differences. This study gives a deeper understanding of the critical proteomic changes associated with renal obstruction and represents the deepest proteomic profile of renal obstruction to date.

Indexed as

AdolescentBiomarkersChildChild, PreschoolFemaleHumansInfantKidneyMaleProtein Interaction MapsProteomicsUreteral ObstructionUrinary BladderBiomarkers

Identifiers

PMID27215552
PMCPMC4974339

What OpenQuestion 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 OpenQuestion graph.