Evidence map›Paper›PMID 28905229›Full record

ArticleDiabetologia2017

Increased plasma N-glycome complexity is associated with higher risk of type 2 diabetes.

Toma Keser, Ivan Gornik, Frano Vučković, Najda Selak, Tamara Pavić, Edita Lukić, Ivan Gudelj, Hrvoje Gašparović, Bojan Biočina, Therese Tilin and 11 more

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
8.8field-weighted citation impact, top 2% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 106 citations in OpenAlex.

  1. Pooled it
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  7. The Human BloodJACS Au · 2024
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  8. Article
  9. Article
  10. Review
  11. Review
  12. Observational
  13. Article
  14. Article
  15. Article
  16. Article
  17. High-Throughput Glycomic Methods.Chemical reviews · 2022
    Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 7 institutions in 6 countries.

Toma KeserUniversity of Zagreb Faculty of Pharmacy and Biochemistry, Ante Kovačića 1, 10 000, Zagreb, Croatia.
Ivan GornikClinical Hospital Centre Zagreb, Zagreb, Croatia.
Frano VučkovićGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Najda SelakUniversity of Zagreb Faculty of Pharmacy and Biochemistry, Ante Kovačića 1, 10 000, Zagreb, Croatia.
Tamara PavićUniversity of Zagreb Faculty of Pharmacy and Biochemistry, Ante Kovačića 1, 10 000, Zagreb, Croatia.
Edita LukićClinical Hospital Centre Zagreb, Zagreb, Croatia.
Ivan GudeljGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Hrvoje GašparovićDepartment of Cardiac Surgery, University Hospital Center Zagreb, University of Zagreb School of Medicine, Zagreb, Croatia.
Bojan BiočinaDepartment of Cardiac Surgery, University Hospital Center Zagreb, University of Zagreb School of Medicine, Zagreb, Croatia.
Therese TilinInstitute of Cardiovascular Science, University College London, London, UK.
Annika WennerströmNational Institute for Health and Welfare (THL), Helsinki, Finland.
Satu MännistöNational Institute for Health and Welfare (THL), Helsinki, Finland.
Veikko SalomaaNational Institute for Health and Welfare (THL), Helsinki, Finland.
Aki HavulinnaNational Institute for Health and Welfare (THL), Helsinki, Finland.
Wei WangSchool of Medical and Health Sciences, Edith Cowan University, Perth, Australia.
James F WilsonCentre for Global Health Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.
Nish ChaturvediInstitute of Cardiovascular Science, University College London, London, UK.
Markus PerolaNational Institute for Health and Welfare (THL), Helsinki, Finland.
Harry CampbellCentre for Global Health Research, Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.
Gordan LaucUniversity of Zagreb Faculty of Pharmacy and Biochemistry, Ante Kovačića 1, 10 000, Zagreb, Croatia.
Olga GornikUniversity of Zagreb Faculty of Pharmacy and Biochemistry, Ante Kovačića 1, 10 000, Zagreb, Croatia. ogornik@pharma.hr.
Finnish Institute for Health and Welfare · FIUniversity of Zagreb · HRUniversity Hospital Centre Zagreb · HRScience Research Laboratory · USUniversity College London · GBUniversity of Edinburgh · GBCapital Medical University · CN

Funding

British Heart Foundation CS/13/1/30327British Heart Foundation SP/07/001/23603Diabetes UK 13/0004774Wellcome Trust WT082464
6 · The paper itself

Abstract

aims/hypothesisBetter understanding of type 2 diabetes and its prevention is a pressing need. Changes in human plasma N-glycome are associated with many diseases and represent promising diagnostic and prognostic biomarkers. Variations in glucose metabolism directly affect glycosylation through the hexosamine pathway but studies of plasma glycome in type 2 diabetes are scarce. The aim of this study was to determine whether plasma protein N-glycome is changed in individuals who are at greater risk of developing type 2 diabetes.

methodsUsing a chromatographic approach, we analysed N-linked glycans from plasma proteins in two populations comprising individuals with registered hyperglycaemia during critical illness (increased risk for development of type 2 diabetes) and individuals who stayed normoglycaemic during the same condition: AcuteInflammation (59 cases vs 49 controls) and AcuteInflammation Replication (52 cases vs 14 controls) populations. N-glycome was also studied in individuals from FinRisk (37 incident cases of type 2 diabetes collected at baseline vs 37 controls), Orkney Complex Disease Study (ORCADES; 94 individuals with HbA

resultsIndividuals with increased risk for diabetes type 2 development (AcuteInflammation and AcuteInflammation Replication populations), incident cases of type 2 diabetes collected at baseline (FinRisk population) and individuals with elevated HbA CONCLUSIONS/

interpretationIncreased complexity of plasma N-glycan structures is associated with higher risk of developing type 2 diabetes and poorer regulation of blood glucose levels. Although further research is needed, this finding could offer a potential new approach for improvement in prevention of diabetes and its complications.

Indexed as

AdultAgedAged, 80 and overBlood GlucoseDiabetes Mellitus, Type 2FemaleGlycated HemoglobinGlycosylationHumansHyperglycemiaMaleMiddle AgedPolysaccharidesPregnancyYoung AdultBlood GlucoseGlycated HemoglobinPolysaccharidesDiabetes predispositionHyperglycaemiaN-linked glycansPlasma N-glycomeType 2 diabetes

Identifiers

PMID28905229
OpenAlexW2755746995

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.