Evidence map›Paper›PMID 32146472›Full record

ArticleAmerican journal of nephrology2020

Adverse Effects of Autoclaved Diets on the Progression of Chronic Kidney Disease and Chronic Kidney Disease-Mineral Bone Disorder in Rats.

Annabel Biruete, Shruthi Srinivasan, Kalisha D O'Neill, Colby J Vorland, Kathleen M Hill Gallant, Weijing Cai, Jaime Uribarri, Nancy Johnston, Matthew R Allen, Neal X Chen and 1 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in American journal of nephrology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. 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

11 authors at 4 institutions in 1 country.

Annabel BirueteDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Shruthi SrinivasanDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Kalisha D O'NeillDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Colby J VorlandDepartment of Applied Health Science, School of Public Health-Bloomington, Indiana University, Bloomington, Indiana, USA.
Kathleen M Hill GallantDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Weijing CaiDivision of Nephrology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Jaime UribarriDivision of Nephrology, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Nancy JohnstonLaboratory Animal Resource Center, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Matthew R AllenDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Neal X ChenDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Sharon M MoeDivision of Nephrology, Indiana University School of Medicine, Indianapolis, Indiana, USA, smoe@iu.edu.
Indiana University School of MedicineIcahn School of Medicine at Mount Sinai · USPurdue University West Lafayette · USRichard L. Roudebush VA Medical Center · US

Funding

Quality Assurance and Quality Control Project Management: Improving Submissions and Study Conduct in the Human Subjects Research Prior Approval ProcessUL1TR002529 · NCATS · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M, WIEHE, SARAH ELIZABETH · 2018 to 2022
$27.2M
Resource CoreP30AR072581 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI STUART J WARDEN · 2017 to 2026
$8.3M
Comprehensive Training Program in Musculoskeletal ResearchT32AR065971 · NIAMS · INDIANA UNIVERSITY INDIANAPOLIS · PI ALEXANDER G ROBLING · 2015 to 2026
$4.4M
Pathogenesis of compromised bone quality and mechanics in chronic kidney disease.R01DK110871 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI ALLEN, MATTHEW R, MOE, SHARON M · 2016 to 2019
$1.8M
Indiana University Kidney Training Program (IU-KTP)T32DK120524 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI MOE, SHARON M · 2019 to 2023
$1.3M
Phosphorus Absorption and Balance in Normal Physiology and Chronic Kidney DiseaseK01DK102864 · NIDDK · UNIVERSITY OF MINNESOTA · PI GALLANT, KATHLEEN M HILL · 2015 to 2019
$692k
The Mechanism of Uremia Induced Vascular CalcificationI01BX001471 · VA · RLR VA MEDICAL CENTER · PI MOE, SHARON M · 2012 to 2020
–
BLRD VA I01 BX001471NCATS NIH HHS UL1 TR002529NIAMS NIH HHS P30 AR072581NIAMS NIH HHS T32 AR065971NIDDK NIH HHS K01 DK102864NIDDK NIH HHS R01 DK110871NIDDK NIH HHS T32 DK120524
6 · The paper itself

Abstract

backgroundAutoclaving rodent diets is common in laboratory animals, but autoclaving increases the formation of dietary advanced glycation end-products (AGE). We studied the effect of autoclaved (AC) diet alone or in combination with a diet high in bioavailable phosphorus on biochemistries of chronic kidney disease-mineral and bone disorder (CKD-MBD), intestinal gene expression, and oxidative stress.

methodsMale CKD rats (Cy/+) and normal littermates were fed 1 of 3 diets: AC 0.7% phosphorus grain-based diet for 28 weeks (AC); AC diet for 17 weeks followed by non-autoclaved (Non-AC) 0.7% phosphorus casein diet until 28 weeks (AC + Casein); or Non-AC diet for 16 weeks followed by a Non-AC purified diet until 30 weeks (Non-AC + Casein).

resultsAC diets contained ~3× higher AGEs and levels varied depending on the location within the autoclave. Rats fed the AC and AC + Casein diets had higher total AGEs and oxidative stress, irrespective of kidney function. Kidney function was more severely compromised in CKD rats fed AC or AC + Casein compared to Non-AC + Casein. There was a disease-by-diet interaction for plasma phosphorus, parathyroid hormone, and c-terminal fibroblast growth factor-23, driven by high values in the CKD rats fed the AC + Casein diet. Compared to Non-AC + Casein, AC and AC + Casein-fed groups had increased expression of receptor of AGEs and intestinal NADPH oxidase dual oxidase-2, independent of kidney function.

conclusionsAutoclaving rodent diets impacts the progression of CKD and CKD-MBD, highlighting the critical importance of standardizing diets in experiments.

Indexed as

Animal FeedAnimalsChronic Kidney Disease-Mineral and Bone DisorderDisease Models, AnimalDisease ProgressionGlycation End Products, AdvancedHot TemperatureHumansMaleOxidative StressRatsRenal Insufficiency, ChronicSterilizationGlycation End Products, AdvancedAdvanced glycation end-productsChronic kidney disease-mineral and bone disorderDietGastrointestinalOxidative stress

Identifiers

PMID32146472
PMCPMC7228841
OpenAlexW3009270317

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.