Evidence map›Paper›PMID 36950027›Full record

ArticleCanadian journal of kidney health and disease2023

Research Letter: Is the 129S1/SvImJ Mouse Strain More Suitable to Study Anticoagulant-Related Nephropathy Than the C57BL/6 Strain?

Ajay Medipally, Min Xiao, Anjali A Satoskar, Laura Biederman, Iouri Ivanov, Galina Mikhalina, Sergey Brodsky

Open access · goldAbstract read
In one paragraph

Article in Canadian journal of kidney health and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 97% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 3 institutions in 1 country.

Ajay MedipallyDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.
Min XiaoDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.
Anjali A SatoskarDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.
Laura BiedermanDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.
Iouri IvanovDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.
Galina MikhalinaRochester Regional Health Nephrology, NY, USA.
Sergey BrodskyDepartment of Pathology, The Ohio State University Wexner Medical Center, Columbus, USA.ORCID https://orcid.org/0000-0003-4570-5883
The Ohio State University Wexner Medical Center · USNationwide Children's Hospital · USUnity Health System · US

Funding

Anticoagulant related nephropathyR01DK117102 · NIDDK · OHIO STATE UNIVERSITY · PI BRODSKY, SERGEY · 2019 to 2023
$1.9M
NIDDK NIH HHS R01 DK117102
6 · The paper itself

Abstract

Background: We have previously demonstrated that excessive anticoagulation with warfarin or dabigatran may result in acute kidney injury with red blood cell (RBC) tubular casts in some patients with chronic kidney disease, and this condition was named anticoagulant-related nephropathy (ARN). 5/6 nephrectomy (5/6NE) rats treated with warfarin or dabigatran reproduce the main pathologic features of human ARN. We had reported that 5/6NE C57BL/6 mice only partially develop ARN with increased serum creatinine and hematuria but no RBC tubular casts in the kidney. Objectives: The aim of this study was to investigate whether ARN can develop in 5/6NE 129S1/SvImJ mice. Methods: 5/6NE was performed in 129S1/SvImJ mice. Three weeks after 5/6NE, mice were treated with warfarin (1.0 and 1.5 mg/kg/day) or vehicle for 7 days. Serum creatinine, hematuria, and prothrombin time (PT) were monitored daily. Renal morphology was evaluated at the end of the studies. Results: Treatment with warfarin resulted in PT elevation 2 to 3 folds from baseline (1.0 mg/kg/day warfarin) and 4 to 5 folds from baseline (1.5 mg/kg/day warfarin) by day 7. Serum creatinine and hematuria elevated by day 7 in a dose-dependent manner. Histologically, 2 of 8 (25%) 5/6NE mice had RBCs in the tubules, and there was acute tubular epithelial cell injury in all warfarin-treated 5/6NE 129S1/SvImJ mice. Conclusions: Our findings suggest that 129S1/SvImJ mouse strain is a more suitable murine model to study ARN than C57BL/6 mouse strain.

Indexed as

acute kidney injuryanticoagulant-related nephropathyhematuriamouse strainrenal pathology

Identifiers

PMID36950027
PMCPMC10026089
OpenAlexW4327791008

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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.