Evidence map›Paper›PMID 29581235›Full record

ArticleThe Journal of biological chemistry2018

Myeloperoxidase-derived oxidants damage artery wall proteins in an animal model of chronic kidney disease-accelerated atherosclerosis.

Lixia Zeng, Anna V Mathew, Jaeman Byun, Kevin B Atkins, Frank C Brosius, Subramaniam Pennathur

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

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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.

Lixia ZengDepartment of Medicine, Division of Nephrology, Ann Arbor, Michigan 48105.
Anna V MathewDepartment of Medicine, Division of Nephrology, Ann Arbor, Michigan 48105.
Jaeman ByunDepartment of Medicine, Division of Nephrology, Ann Arbor, Michigan 48105.
Kevin B AtkinsDepartment of Medicine, Division of Nephrology, Ann Arbor, Michigan 48105.
Frank C BrosiusDepartment of Medicine, Division of Nephrology, Ann Arbor, Michigan 48105; Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48105.
Subramaniam PennathurDepartment of Medicine, Division of Nephrology, Ann Arbor, Michigan 48105; Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan 48105. Electronic address: spennath@umich.edu.
Michigan Medicine · USUniversity of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID P OLSON · 2013 to 2026
$24.3M
Pilot and Feasibility (P and F) ProgramP30DK089503 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Kanakadurga Singer · 2010 to 2026
$20.3M
University of Michigan O'Brien Kidney Translational Core CenterP30DK081943 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BROSIUS, FRANK C · 2008 to 2022
$12.9M
Myeloperoxidase, Chronic Kidney Disease and AtherosclerosisK08HL130944 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MATHEW, ANNA VACHAPARAMPIL · 2016 to 2021
$893k
NHLBI NIH HHS K08 HL130944NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK081943NIDDK NIH HHS P30 DK089503
6 · The paper itself

Abstract

Increased myeloperoxidase (MPO) levels and activity are associated with increased cardiovascular risk among individuals with chronic kidney disease (CKD). However, a lack of good animal models for examining the presence and catalytic activity of MPO in vascular lesions has impeded mechanistic studies into CKD-associated cardiovascular diseases. Here, we show for the first time that exaggerated atherosclerosis in a pathophysiologically relevant CKD mouse model is associated with increased macrophage-derived MPO activity. Male 7-week-old LDL receptor-deficient mice underwent sham (control mice) or 5/6 nephrectomy and were fed either a low-fat or high-fat, high-cholesterol diet for 24 weeks, and the extents of atherosclerosis and vascular reactivity were assessed. MPO expression and oxidation products-protein-bound oxidized tyrosine moieties 3-chlorotyrosine, 3-nitrotyrosine, and

Indexed as

AnimalsAortaAtherosclerosisBlood Urea NitrogenCreatinineDietary FatsDiet, Fat-RestrictedDiet, High-FatDisease Models, AnimalDisease ProgressionKidney Failure, ChronicKidney Function TestsLipidsLipoproteinsMacrophagesMale3-chlorotyrosine3-nitrotyrosineCreatinineDietary FatsLipidsLipoproteinsMuscle ProteinsOxidantsParathyroid HormonePeroxidaseReceptors, LDLTyrosine3-chlorotyrosine3-nitrotyrosineatherosclerosisChronic Kidney Diseasemacrophagemass spectrometry (MS)myeloperoxidaseoxidative stressoxidized amino acids

Identifiers

PMID29581235
PMCPMC5949994
OpenAlexW2792351762

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.