Evidence map›Paper›PMID 31408493›Full record

Observational studyPloS one2019

Relations of advanced glycation endproducts and dicarbonyls with endothelial dysfunction and low-grade inflammation in individuals with end-stage renal disease in the transition to renal replacement therapy: A cross-sectional observational study.

Remy J H Martens, Natascha J H Broers, Bernard Canaud, Maarten H L Christiaans, Tom Cornelis, Adelheid Gauly, Marc M H Hermans, Constantijn J A M Konings, Frank M van der Sande, Jean L J M Scheijen and 4 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Advanced Glycation End Products and Inflammatory Cytokine Profiles in Maintenance Hemodialysis Patients After the Ingestion of a Protein-Dense Meal.Journal of renal nutrition : the official journal of the Council on Renal Nutrition of the National Kidney Foundation · 2023
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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

14 authors at 8 institutions in 4 countries.

Remy J H MartensDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, the Netherlands.ORCID 0000-0003-4632-6412
Natascha J H BroersDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, the Netherlands.
Bernard CanaudMedical Office EMEA, Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.
Maarten H L ChristiaansDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, the Netherlands.ORCID 0000-0003-3558-2277
Tom CornelisDepartment of Nephrology, Jessa Hospital, Hasselt, Belgium.
Adelheid GaulyMedical Office EMEA, Fresenius Medical Care Deutschland GmbH, Bad Homburg, Germany.ORCID 0000-0002-2554-0711
Marc M H HermansDepartment of Internal Medicine, Division of Nephrology, Viecuri Medical Center, Venlo, the Netherlands.
Constantijn J A M KoningsDepartment of Internal Medicine, Division of Nephrology, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.
Frank M van der SandeDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, the Netherlands.
Jean L J M ScheijenCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, the Netherlands.
Frank StifftDepartment of Internal Medicine, Division of Nephrology, Zuyderland Medical Center, Sittard-Geleen, the Netherlands.
Joris J J M WirtzDepartment of Internal Medicine, Division of Nephrology, St. Laurentius Hospital, Roermond, the Netherlands.
Jeroen P KoomanDepartment of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, the Netherlands.
Casper G SchalkwijkCARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, the Netherlands.
Maastricht University · NLFresenius Medical Care (Germany) · DEJessa Hospital · BELaurentius Ziekenhuis · NLRadboud University Nijmegen · NLUniversité de Montpellier · FRVieCuri Medisch Centrum · NLZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular disease (CVD) related mortality and morbidity are high in end-stage renal disease (ESRD). The pathophysiology of CVD in ESRD may involve non-traditional CVD risk factors, such as accumulation of advanced glycation endproducts (AGEs), dicarbonyls, endothelial dysfunction (ED) and low-grade inflammation (LGI). However, detailed data on the relation of AGEs and dicarbonyls with ED and LGI in ESRD are limited.

methodsWe examined cross-sectional Spearman's rank correlations of AGEs and dicarbonyls with serum biomarkers of ED and LGI in 43 individuals with chronic kidney disease (CKD) stage 5 not on dialysis (CKD5-ND). Free and protein-bound serum AGEs (N∈-(carboxymethyl)lysine (CML), N∈-(carboxyethyl)lysine (CEL), Nδ-(5-hydro-5-methyl-4-imidazolon-2-yl)ornithine (MG-H1)) and serum dicarbonyls (glyoxal, methylglyoxal, 3-deoxyglucosone) were analyzed with tandem mass spectrometry, and tissue AGE accumulation was estimated by skin autofluorescence (SAF). Further, serum biomarkers of ED and LGI included sVCAM-1, sE-selectin, sP-selectin, sThrombomodulin, sICAM-1, sICAM-3, hs-CRP, SAA, IL-6, IL-8 and TNF-α.

resultsAfter adjustment for age, sex and diabetes status, protein-bound CML was positively correlated with sVCAM-1; free CEL with sVCAM-1 and sThrombomodulin; glyoxal with sThrombomodulin; and methylglyoxal with sVCAM-1 (correlation coefficients ranged from 0.36 to 0.44). In addition, free CML was positively correlated with SAA; protein-bound CML with IL-6; free CEL with hs-CRP, SAA and IL-6; free MG-H1 with SAA; protein-bound MG-H1 with IL-6; and MGO with hs-CRP and IL-6 (correlation coefficients ranged from 0.33 to 0.38). Additional adjustment for eGFR attenuated partial correlations of serum AGEs and serum dicarbonyls with biomarkers of ED and LGI.

conclusionsIn individuals with CKD5-ND, higher levels of serum AGEs and serum dicarbonyls were related to biomarkers of ED and LGI after adjustment for age, sex and diabetes mellitus. Correlations were attenuated by eGFR, suggesting that eGFR confounds and/or mediates the relation of serum AGEs and dicarbonyls with ED and LGI.

Indexed as

Diabetes MellitusKidney Failure, ChronicRenal DialysisAdultAgedBiomarkersCross-Sectional StudiesDeoxyglucoseEndothelium, VascularFemaleGlycation End Products, AdvancedGlyoxalHumansLysineMaleMiddle Aged3-deoxyglucosoneBiomarkersDeoxyglucoseGlycation End Products, AdvancedGlyoxalLysineN(6)-carboxyethyllysineN(6)-carboxymethyllysineOrnithine

Identifiers

PMID31408493
PMCPMC6692010
OpenAlexW2967627151

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.