Evidence map›Paper›PMID 20219828›Full record

ArticleAmerican journal of physiology. Renal physiology2010

Heterogeneous stock rats: a new model to study the genetics of renal phenotypes.

Leah C Solberg Woods, Cary Stelloh, Kevin R Regner, Tiffany Schwabe, Jessica Eisenhauer, Michael R Garrett

Abstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

29 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Bisphenol F Exposure in Adolescent Heterogeneous Stock Rats Affects Growth and Adiposity.Toxicological sciences : an official journal of the Society of Toxicology · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Using Heterogeneous Stocks for Fine-Mapping Genetically Complex Traits.Methods in molecular biology (Clifton, N.J.) · 2019
    Review
  15. Article
  16. Article
  17. Heterogeneous Stock Populations for Analysis of Complex Traits.Methods in molecular biology (Clifton, N.J.) · 2017
    Article
  18. Article
  19. Article
  20. Nephron Deficiency and Predisposition to Renal Injury in a Novel One-Kidney Genetic Model.Journal of the American Society of Nephrology : JASN · 2015
    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

6 authors at 2 institutions in 1 country.

Leah C Solberg WoodsDepartment of Pediatrics, Medical College of Wisconsin, Milwaukee, Wisconsin 53226, USA.
Cary Stelloh
Kevin R Regner
Tiffany Schwabe
Jessica Eisenhauer
Michael R Garrett
Colorado Kidney Care · USMedical College of Wisconsin · US

Funding

Genetics of Renal End Organ Damage in HypertensionR01HL094446 · NHLBI · UNIVERSITY OF MISSISSIPPI MED CTR · PI GARRETT, MICHAEL R · 2009 to 2013
$1.8M
Fine mapping NIDDM QTL 1 using heterogeneous stock ratsK01DK076977 · NIDDK · MEDICAL COLLEGE OF WISCONSIN · PI SOLBERG WOODS, LEAH CATHERINE · 2007 to 2009
$385k
NHLBI NIH HHS HL-094446NHLBI NIH HHS R01 HL094446NIDDK NIH HHS K01 DK076977NIDDK NIH HHS K01-DK-076977
6 · The paper itself

Abstract

Chronic kidney disease is a growing medical concern, with an estimated 25.6 million people in the United States exhibiting some degree of kidney injury and/or decline in kidney function. Animal models provide great insight into the study of the genetics of complex diseases. In particular, heterogeneous stock (HS) rats represent a unique genetic resource enabling rapid fine-mapping of complex traits. However, they have not been explored as a model to study renal phenotypes. To evaluate the usefulness of HS rats in the genetics of renal traits, a time course evaluation (weeks 8-40) was performed for several renal phenotypes. As expected, a large degree of variation was seen for most renal traits. By week 24, three (of 40) rats exhibited marked proteinuria that increased gradually until week 40 and ranged from 33.7 to 80.2 mg/24 h. Detailed histological analysis confirmed renal damage in these rats. In addition, several rats consistently exhibited significant hematuria (5/41). Interestingly, these rats were not the same rats that exhibited proteinuria, indicating that susceptibility to different types of kidney injury is likely segregating within the HS population. One HS rat exhibited unilateral renal agenesis (URA), which was accompanied by a significant degree of proteinuria and glomerular and tubulointerstitial injury. The parents of this HS rat were identified and bred further. Additional offspring of this pair were observed to exhibit URA at frequency between 40% and 60%. In summary, these novel data demonstrate that HS rats exhibit variation in proteinuria and other kidney-related traits, confirming that the model harbors susceptibility alleles for kidney injury and providing the basis for further genetic studies.

Indexed as

Genetic VariationQuantitative Trait, HeritableAnimalsBlood Urea NitrogenChronic DiseaseCreatinineDisease Models, AnimalDisease ProgressionGenetic Predisposition to DiseaseGlycosuria, RenalHematuriaHeterozygoteKidneyKidney DiseasesPhenotypeProteinuriaCreatinine

Identifiers

PMID20219828
PMCPMC2886820
OpenAlexW2171246514

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.