Evidence map›Paper›PMID 33941843›Full record

ArticleInternational journal of obesity (2005)2021

Extensive weight loss reduces glycan age by altering IgG N-glycosylation.

Valentina L Greto, Ana Cvetko, Tamara Štambuk, Niall J Dempster, Domagoj Kifer, Helena Deriš, Ana Cindrić, Frano Vučković, Mario Falchi, Richard S Gillies and 8 more

Open access · hybridAbstract read
In one paragraph

Article in International journal of obesity (2005), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Article
  7. Immunoglobulin G in aging and cancer.Frontiers in immunology · 2026
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Glycosylation in aging and neurodegenerative diseases.Acta biochimica et biophysica Sinica · 2024
    Review
  19. Article
  20. 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

18 authors at 5 institutions in 3 countries.

Valentina L Greto *Translational Gastroenterology Unit and NIHR Oxford Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.ORCID http://orcid.org/0000-0002-0155-1846
Ana Cvetko *Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.ORCID http://orcid.org/0000-0002-7134-2484
Tamara Štambuk *Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.
Niall J DempsterOxford Centre for Diabetes and NIHR Oxford Biomedical Research Centre, Endocrinology and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Domagoj KiferFaculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.
Helena DerišGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Ana CindrićGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Frano VučkovićGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Mario FalchiThe Department of Twin Research, King's College London, St Thomas' Hospital, London, UK.
Richard S GilliesDepartment of Upper GI Surgery, Oxford University Hospitals, Oxford, UK.
Jeremy W TomlinsonOxford Centre for Diabetes and NIHR Oxford Biomedical Research Centre, Endocrinology and Metabolism, Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
Olga GornikFaculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia.
Bruno SgromoDepartment of Upper GI Surgery, Oxford University Hospitals, Oxford, UK.
Tim D SpectorThe Department of Twin Research, King's College London, St Thomas' Hospital, London, UK.
Cristina Menni *The Department of Twin Research, King's College London, St Thomas' Hospital, London, UK.ORCID http://orcid.org/0000-0001-9790-0571
Alessandra Geremia *Translational Gastroenterology Unit and NIHR Oxford Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Carolina V Arancibia-Cárcamo *Translational Gastroenterology Unit and NIHR Oxford Biomedical Research Centre, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Gordan Lauc *Faculty of Pharmacy and Biochemistry, University of Zagreb, Zagreb, Croatia. glauc@pharma.hr.ORCID http://orcid.org/0000-0003-1840-9560
University of Oxford · GBUniversity of Zagreb · HRGenos (Croatia) · HRSt Thomas' Hospital · GBOxford University Hospitals NHS Trust · GB

Funding

Medical Research Council MR/P011462/1
6 · The paper itself

Abstract

backgroundObesity, a major global health problem, is associated with increased cardiometabolic morbidity and mortality. Protein glycosylation is a frequent posttranslational modification, highly responsive to inflammation and ageing. The prospect of biological age reduction, by changing glycosylation patterns through metabolic intervention, opens many possibilities. We have investigated whether weight loss interventions affect inflammation- and ageing-associated IgG glycosylation changes, in a longitudinal cohort of bariatric surgery patients. To support potential findings, BMI-related glycosylation changes were monitored in a longitudinal twins cohort.

methodsIgG N-glycans were chromatographically profiled in 37 obese patients, subjected to low-calorie diet, followed by bariatric surgery, across multiple timepoints. Similarly, plasma-derived IgG N-glycan traits were longitudinally monitored in 1680 participants from the TwinsUK cohort.

resultsLow-calorie diet induced a marked decrease in the levels of IgG N-glycans with bisecting GlcNAc, whose higher levels are usually associated with ageing and inflammatory conditions. Bariatric surgery resulted in extensive alterations of the IgG N-glycome that accompanied progressive weight loss during 1-year follow-up. We observed a significant increase in digalactosylated and sialylated glycans, and a substantial decrease in agalactosylated and core fucosylated IgG N-glycans (adjusted p value range 7.38 × 10

conclusionsAltogether, these findings highlight that weight loss substantially affects IgG N-glycosylation, resulting in reduced glycan and biological age.

Indexed as

Immunoglobulin GObesityAdultAgingBariatric SurgeryBody Mass IndexFemaleGlycoproteinsGlycosylationHumansLongitudinal StudiesMaleMiddle AgedTwinsWeight LossGlycoproteinsglycosylated IgGImmunoglobulin G

Identifiers

PMID33941843
PMCPMC8236401
OpenAlexW3158793813

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.