Evidence map›Paper›PMID 28468961›Full record

ArticleAmerican journal of physiology. Renal physiology2017

Urine RAS components in mice and people with type 1 diabetes and chronic kidney disease.

Jan Wysocki, Anne Goodling, Mar Burgaya, Kathryn Whitlock, John Ruzinski, Daniel Batlle, Maryam Afkarian

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 4% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  13. SARS- CoV-2 infection and oxidative stress in early-onset preeclampsia.Biochimica et biophysica acta. Molecular basis of disease · 2022
    Review
  14. Mitochondrial Pathophysiology on Chronic Kidney Disease.International journal of molecular sciences · 2022
    Review
  15. Review
  16. Novel roles of the renal angiotensin-converting enzyme.Molecular and cellular endocrinology · 2021
    Review
  17. Review
  18. Review
  19. Article
  20. An update on ACE2 amplification and its therapeutic potential.Acta physiologica (Oxford, England) · 2021
    Review
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

7 authors at 4 institutions in 1 country.

Jan WysockiDivision of Nephrology and Hypertension, Department of Medicine, The Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Anne GoodlingKidney Research Institute and Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington.
Mar BurgayaDivision of Nephrology and Hypertension, Department of Medicine, The Feinberg School of Medicine, Northwestern University, Chicago, Illinois.
Kathryn WhitlockCenter for Child Health, Behavior and Development, Seattle Children's Research Institute, Seattle, Washington; and.
John RuzinskiKidney Research Institute and Division of Nephrology, Department of Medicine, University of Washington, Seattle, Washington.
Daniel BatlleDivision of Nephrology and Hypertension, Department of Medicine, The Feinberg School of Medicine, Northwestern University, Chicago, Illinois; mafkarian@ucdavis.edu.
Maryam AfkarianDivision of Nephrology, Department of Medicine, University of California, Davis, California mafkarian@ucdavis.edu.
Northwestern University · USUniversity of Washington · USSeattle Children's Hospital · USUniversity of California, Davis · US

Funding

Strategies for ACE2 Amplification to Treat Diabetic Kidney DiseaseR01DK080089 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BATLLE, DANIEL · 2009 to 2012
$1.3M
Urinary Renin Angiotensin System in DiabetesR01DK104785 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BATLLE, DANIEL · 2015 to 2017
$939k
NIDDK NIH HHS R01 DK080089NIDDK NIH HHS R01 DK104785
6 · The paper itself

Abstract

The pathways implicated in diabetic kidney disease (DKD) are largely derived from animal models. To examine if alterations in renin-angiotensin system (RAS) in humans are concordant with those in rodent models, we measured concentration of angiotensinogen (AOG), cathepsin D (CTSD), angiotensin-converting enzyme (ACE), and ACE2 and enzymatic activities of ACE, ACE2, and aminopeptidase-A in FVB mice 13-20 wk after treatment with streptozotocin (

Indexed as

Renin-Angiotensin SystemAdultAngiotensin-Converting Enzyme InhibitorsAnimalsBiomarkersDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetic NephropathiesEnzymesFemaleHumansMaleMiceMiddle AgedPredictive Value of TestsRenal Insufficiency, ChronicAngiotensin-Converting Enzyme InhibitorsBiomarkersEnzymesaminopeptidase-Aangiotensin-converting enzymeangiotensin-converting enzyme 2angiotensinogencathepsin Ddiabetic kidney diseaserenin-angiotensin system

Identifiers

PMID28468961
PMCPMC5582909
OpenAlexW2610914416

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.