Evidence map›Paper›PMID 37400796›Full record

ReviewBMC medicine2023

Plasma protein N-glycome composition associates with postprandial lipaemic response.

Panayiotis Louca, Tamara Štambuk, Azra Frkatović-Hodžić, Ana Nogal, Massimo Mangino, Sarah E Berry, Helena Deriš, George Hadjigeorgiou, Jonathan Wolf, Martina Vinicki and 5 more

Open access · goldAbstract readReview
In one paragraph

Review in BMC medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

15 authors at 7 institutions in 4 countries.

Panayiotis Louca *Department of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital Campus, Westminster Bridge Road, London, SE1 7EH, UK.
Tamara Štambuk *Genos Glycoscience Research Laboratory, Zagreb, Croatia.
Azra Frkatović-Hodžić *Genos Glycoscience Research Laboratory, Zagreb, Croatia.
Ana NogalDepartment of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital Campus, Westminster Bridge Road, London, SE1 7EH, UK.
Massimo ManginoDepartment of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital Campus, Westminster Bridge Road, London, SE1 7EH, UK.
Sarah E BerryDepartment of Nutritional Sciences, King's College London, Franklin Wilkins Building, London, SE1 9NH, UK.
Helena DerišGenos Glycoscience Research Laboratory, Zagreb, Croatia.
George HadjigeorgiouZOE Ltd, London, UK.
Jonathan WolfZOE Ltd, London, UK.
Martina VinickiGenos Glycoscience Research Laboratory, Zagreb, Croatia.
Paul W FranksLund University Diabetes Center, Lund University, Malmö, Sweden.
Ana M ValdesAcademic Rheumatology Clinical Sciences Building, Nottingham City Hospital, University of Nottingham, Nottingham, UK.
Tim D SpectorDepartment of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital Campus, Westminster Bridge Road, London, SE1 7EH, UK.
Gordan Lauc *Genos Glycoscience Research Laboratory, Zagreb, Croatia.
Cristina Menni *Department of Twin Research and Genetic Epidemiology, King's College London, St Thomas' Hospital Campus, Westminster Bridge Road, London, SE1 7EH, UK. cristina.menni@kcl.ac.uk.ORCID 0000-0001-9790-0571
St Thomas' Hospital · GBGenos (Croatia) · HRZOE (United Kingdom) · GBKing's College London · GBLund University · SEUniversity of Nottingham · GBUniversity of Zagreb · HR

Funding

Medical Research Council MR/W026813/1Wellcome Trust
6 · The paper itself

Abstract

backgroundA dysregulated postprandial metabolic response is a risk factor for chronic diseases, including type 2 diabetes mellitus (T2DM). The plasma protein N-glycome is implicated in both lipid metabolism and T2DM risk. Hence, we first investigate the relationship between the N-glycome and postprandial metabolism and then explore the mediatory role of the plasma N-glycome in the relationship between postprandial lipaemia and T2DM.

methodsWe included 995 individuals from the ZOE-PREDICT 1 study with plasma N-glycans measured by ultra-performance liquid chromatography at fasting and triglyceride, insulin, and glucose levels measured at fasting and following a mixed-meal challenge. Linear mixed models were used to investigate the associations between plasma protein N-glycosylation and metabolic response (fasting, postprandial (C

resultsWe identified 36 out of 55 glycans significantly associated with postprandial triglycerides (C

conclusionsThis study provides a comprehensive overview of the interconnections between plasma protein N-glycosylation and postprandial responses, demonstrating the incremental predictive benefit of N-glycans. We also suggest a considerable proportion of the effect of prediabetes on postprandial triglycerides is mediated by some plasma N-glycans.

Indexed as

Diabetes Mellitus, Type 2HyperlipidemiasPrediabetic StateBlood GlucoseBlood ProteinsHumansInsulinPolysaccharidesTriglyceridesBlood GlucoseBlood ProteinsInsulinPolysaccharidesTriglyceridesMetabolic responsePlasma N-glycomePostprandial glycaemiaPostprandial lipaemiaProtein glycosylation

Identifiers

PMID37400796
PMCPMC10318725
OpenAlexW4382938190

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.