Evidence map›Paper›PMID 31514489›Full record

ArticleJournal of clinical research in pediatric endocrinology2020

Soluble Receptor for Glycation End-products Concentration Increases Following the Treatment of Severe Diabetic Ketoacidosis

William H. Hoffman, Takaki Ishikawa, James Blum, Naoto Tani, Tomoya Ikeda, Carol M. Artlett

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
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 4 institutions in 2 countries.

William H. HoffmanAugusta University, Medical College of Georgia, Department of Pediatrics, Georgia, USAORCID 0000-0002-7800-0532
Takaki IshikawaOsaka City University Faculty of Medicine, Department of Legal Medicine, Abeno Osaka, JapanORCID 0000-0002-4349-9740
James BlumUniversity of North Carolina-Wilmington, Department of Mathematics and Statistics, North Carolina, USAORCID 0000-0003-3060-1942
Naoto TaniOsaka City University Faculty of Medicine, Department of Legal Medicine, Abeno Osaka, JapanORCID 0000-0002-4981-0456
Tomoya IkedaOsaka City University Faculty of Medicine, Department of Legal Medicine, Abeno Osaka, JapanORCID 0000-0003-3262-3141
Carol M. ArtlettDrexel University College of Medicine, Department of Microbiology and Immunology, Pennsylvania, USAORCID 0000-0002-9060-0581
Osaka City University · JPAugusta University · USOwl Research Institute · USUniversity of North Carolina Wilmington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To determine the time relationships of soluble receptor for glycation end-products (sRAGE), [a decoy of the advanced glycation end-products (AGE)-RAGE axis] and D-lactate, (a metabolite of methylglyoxal) in the inflammatory response to diabetic ketoacidosis (DKA). Methods: Sixteen children and adolescents with type 1 diabetes (T1D) had blood samples obtained, 6-12 hours into treatment, at three weeks and three months post start of treatment. sRAGE and D-lactate concentrations at three months were considered baseline. Expression of RAGE was investigated in the myocardium of a newly diagnosed and untreated young person with fatal T1D/DKA. Results: sRAGE 6-12 hours after the start of treatment was 39% lower than the values at two weeks (p=0.0036) and at three months (p=0.0023) post treatment. D-lactate was higher during treatment than at three weeks (p=0.04) and at three months (p=0.035). Conclusion: sRAGE concentration was decreased during treatment, compared to concentrations at two weeks and three months after treatment. The increased D-lactate during treatment was in keeping with the known increase in dicarbonyls at this time. The finding of RAGE expression in a young myocardium prior to DKA treatment suggested cardiovascular inflammation pre-treatment and at a young age.

Indexed as

AdolescentChildDiabetes Mellitus, Type 1Diabetic KetoacidosisFemaleGlycation End Products, AdvancedHumansHypoglycemic AgentsInflammationInsulinLactic AcidLongitudinal StudiesMaleMyocarditisReceptor for Advanced Glycation End ProductsSeverity of Illness IndexAGER protein, humanGlycation End Products, AdvancedHypoglycemic AgentsInsulinLactic AcidReceptor for Advanced Glycation End ProductsDiabetic ketoacidosisD-lactatemyocarditissoluble receptor for advanced glycation end-products

Identifiers

PMID31514489
PMCPMC7291407
OpenAlexW2972784633

What Socratic holds

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LicenceCC BY
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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 Socratic graph.