Evidence map›Paper›PMID 26840264›Full record

ArticleOncotarget2016

Identification of novel plasma glycosylation-associated markers of aging.

Mariangela Catera, Vincenzo Borelli, Nadia Malagolini, Mariella Chiricolo, Giulia Venturi, Celso A Reis, Hugo Osorio, Provvidenza M Abruzzo, Miriam Capri, Daniela Monti and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Exploring serumHeliyon · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Age-Related Changes in SerumBiomolecules · 2023
    Article
  9. Article
  10. The role ofFrontiers in immunology · 2023
    Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Glycosylation and Cardiovascular Diseases.Advances in experimental medicine and biology · 2021
    Article
  16. Glycosylation and Aging.Advances in experimental medicine and biology · 2021
    Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 3 institutions in 2 countries.

Mariangela CateraDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Vincenzo BorelliDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Nadia MalagoliniDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Mariella ChiricoloDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Giulia VenturiDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Celso A ReisInstituto de Investigação e Inovação em Saúde (Institute for Research and Innovation in Health), University of Porto, and Institute of Molecular Pathology and Immunology of The University of Porto IPATIMUP), Porto, Portugal.
Hugo OsorioInstituto de Investigação e Inovação em Saúde (Institute for Research and Innovation in Health), University of Porto, and Institute of Molecular Pathology and Immunology of The University of Porto IPATIMUP), Porto, Portugal.
Provvidenza M AbruzzoDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Miriam CapriDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Daniela MontiDipartimento di Scienze Biomediche, Sperimentali e Cliniche "Mario Serio", University of Florence, Florence, Italy.
Rita OstanDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Claudio FranceschiDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
Fabio Dall'OlioDipartimento di Medicina Specialistica Diagnostica e Sperimentale (DIMES) University of Bologna, Bologna, Italy.
University of Bologna · ITi3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto · PTUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pro- or anti-inflammatory activities of immunoglobulins G (IgGs) are controlled by the structure of the glycan N-linked to Asn297 of their heavy chain. The age-associated low grade inflammation (inflammaging) is associated with increased plasmatic levels of agalactosylated IgGs terminating with N-acetylglucosamine (IgG-G0) whose biogenesis has not been fully explained. Although the biosynthesis of glycans is in general mediated by glycosyltransferases associated with internal cell membranes, the extracellular glycosylation of circulating glycoproteins mediated by plasmatic glycosyltransferases has been recently demonstrated. In this study we have investigated the relationship between plasmatic glycosyltransferases, IgG glycosylation and inflammatory and aging markers. In cohorts of individuals ranging from infancy to centenarians we determined the activity of plasmatic β4 galactosyltransferase(s) (B4GALTs) and of α2,6-sialyltransferase ST6GAL1, the glycosylation of IgG, the GlycoAge test (a glycosylation-based marker of aging) and the plasma level of inflammatory and liver damage markers. Our results show that: 1) plasmatic B4GALTs activity is a new marker of aging, showing a linear increase throughout the whole age range. 2) plasmatic ST6GAL1 was high only in children and in people above 80, showing a quadratic relationship with age. 3) Neither plasmatic glycosyltransferase correlated with markers of liver damage. 4) plasmatic ST6GAL1 showed a positive association with acute phase proteins in offspring of short lived parents, but not in centenarians or in their offspring. 5) Although the glycosylation of IgGs was not correlated with the level of the two plasmatic glycosyltransferases, it showed progressive age-associated changes consistent with a shift toward a pro-inflammatory glycotype.

Indexed as

AdolescentAdultAgedAged, 80 and overAgingAntigens, CDbeta-D-Galactoside alpha 2-6-SialyltransferaseBiomarkersChildChild, PreschoolFemaleGalactosyltransferasesGlycoproteinsGlycosylationHumansImmunoglobulin GAntigens, CDbeta-1,4-galactosyltransferase Ibeta-D-Galactoside alpha 2-6-SialyltransferaseBiomarkersGalactosyltransferasesGlycoproteinsglycosylated IgGImmunoglobulin GSialyltransferasesST6GAL1 protein, humanantibody glycosylationGerotargetinflammagingplasma galactosyltransferasesplasma sialyltransferasessoluble glycosyltransferases

Identifiers

PMID26840264
PMCPMC4884931
OpenAlexW2286906488

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.