Evidence map›Paper›PMID 25349207›Full record

ArticleJournal of the American Society of Nephrology : JASN2015

Nephron Deficiency and Predisposition to Renal Injury in a Novel One-Kidney Genetic Model.

Xuexiang Wang, Ashley C Johnson, Jan M Williams, Tiffani White, Alejandro R Chade, Jie Zhang, Ruisheng Liu, Richard J Roman, Jonathan W Lee, Patrick B Kyle and 2 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 25% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  7. Review
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  9. Article
  10. Loss ofHypertension (Dallas, Tex. : 1979) · 2020
    Article
  11. Temporal Expression and Cellular Localization of PAPPA2 in the Developing Kidney of Rat.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
    Article
  12. Article
  13. Article
  14. Article
  15. Single-Nephron Glomerular Filtration Rate in Healthy Adults.The New England journal of medicine · 2017
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
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

12 authors at 2 institutions in 2 countries.

Xuexiang WangDepartments of *Pharmacology and Toxicology.
Ashley C JohnsonDepartments of *Pharmacology and Toxicology.
Jan M WilliamsDepartments of *Pharmacology and Toxicology, Medicine (Nephrology).
Tiffani WhiteDepartments of *Pharmacology and Toxicology.
Alejandro R ChadePhysiology and Biophysics, Radiology, University of Mississippi Medical Center, Jackson, Mississippi; and.
Jie ZhangPhysiology and Biophysics.
Ruisheng LiuPhysiology and Biophysics.
Richard J RomanDepartments of *Pharmacology and Toxicology, Medicine (Nephrology).
Jonathan W LeeDepartments of *Pharmacology and Toxicology.
Patrick B KylePathology, and.
Leah Solberg-WoodsDepartment of Pediatrics, Medical College of Wisconsin, Madison, Wisconsin.
Michael R GarrettDepartments of *Pharmacology and Toxicology, Medicine (Nephrology), mrgarrett@umc.edu.
Institute of Molecular Biology and Biophysics · RUMedical College of Wisconsin · US

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
The role of leptin in autoimmune-associated hypertensionP20GM104357 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI TAYLOR, ERIN BASSFORD · 2013 to 2022
$23.4M
Center for Psychiatric NeuroscienceP30GM103328 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI STOCKMEIER, CRAIG ALLEN · 2013 to 2017
$5.5M
20-HETE-TGF-beta in Hypertension-Induced Renal InjuryR37HL036279 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI ROMAN, RICHARD J. · 2005 to 2014
$4.0M
Microcirculation in Renovascular HypertensionR01HL095638 · NHLBI · UNIVERSITY OF MISSOURI-COLUMBIA · PI CHADE, ALEJANDRO ROBERTO · 2010 to 2021
$3.9M
Genetics of Renal End Organ Damage in HypertensionR01HL094446 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI GARRETT, MICHAEL R · 2009 to 2013
$1.8M
Renal microcirculation and hypertension induced renal injuryR01DK104184 · NIDDK · UNIVERSITY OF MISSISSIPPI MED CTR · PI ROMAN, RICHARD J. · 2014 to 2017
$1.8M
Tubuloglomerular feedback and salt-sensitive hypertensionR01DK098582 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI LIU, RUISHENG · 2013 to 2016
$1.3M
Primary cilia and modulation of the renal microcirculationR01DK099276 · NIDDK · UNIVERSITY OF SOUTH FLORIDA · PI LIU, RUISHENG · 2014 to 2017
$980k
NHLBI NIH HHS R01 HL094446NHLBI NIH HHS R01 HL095638NHLBI NIH HHS R37 HL036279NIDDK NIH HHS R01 DK098582NIDDK NIH HHS R01 DK099276NIDDK NIH HHS R01 DK104184NIGMS NIH HHS P20 GM103476NIGMS NIH HHS P20-GM103476)NIGMS NIH HHS P20 GM104357NIGMS NIH HHS P20-GM104357NIGMS NIH HHS P30 GM103328NIGMS NIH HHS P30-GM103328PHS HHS NIH/NHLBIHL095638
6 · The paper itself

Abstract

Some studies have reported up to 40% of patients born with a single kidney develop hypertension, proteinuria, and in some cases renal failure. The increased susceptibility to renal injury may be due, in part, to reduced nephron numbers. Notably, children who undergo nephrectomy or adults who serve as kidney donors exhibit little difference in renal function compared with persons who have two kidneys. However, the difference in risk between being born with a single kidney versus being born with two kidneys and then undergoing nephrectomy are unclear. Animal models used previously to investigate this question are not ideal because they require invasive methods to model congenital solitary kidney. In this study, we describe a new genetic animal model, the heterogeneous stock-derived model of unilateral renal agenesis (HSRA) rat, which demonstrates 50%-75% spontaneous incidence of a single kidney. The HSRA model is characterized by reduced nephron number (more than would be expected by loss of one kidney), early kidney/glomerular hypertrophy, and progressive renal injury, which culminates in reduced renal function. Long-term studies of temporal relationships among BP, renal hemodynamics, and renal function demonstrate that spontaneous single-kidney HSRA rats are more likely than uninephrectomized normal littermates to exhibit renal impairment because of the combination of reduced nephron numbers and prolonged exposure to renal compensatory mechanisms (i.e., hyperfiltration). Future studies with this novel animal model may provide additional insight into the genetic contributions to kidney development and agenesis and the factors influencing susceptibility to renal injury in individuals with congenital solitary kidney.

Indexed as

Acute Kidney InjuryAdultAnalysis of VarianceAnimalsCausalityChildDisease Models, AnimalDisease ProgressionFemaleGlomerular Filtration RateHumansHypertrophyKidneyMaleModels, GeneticNephrectomychronic kidney diseasegenetics and developmentglomerular hyperfiltrationpediatric nephrologyrenal agenesistranscriptional profiling

Identifiers

PMID25349207
PMCPMC4483580
OpenAlexW2083997280

What OpenQuestion holds

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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.