Evidence map›Paper›PMID 35156387›Full record

ArticleJournal of the American Heart Association2022

Glycoprotein Acetyls: A Novel Inflammatory Biomarker of Early Cardiovascular Risk in the Young.

Scott T Chiesa, Marietta Charakida, Georgios Georgiopoulos, Justin D Roberts, Simon J Stafford, Chloe Park, Juha Mykkänen, Mika Kähönen, Terho Lehtimäki, Mika Ala-Korpela and 8 more

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

67 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  8. Association of Glycoprotein Acetylation With Carotid-Femoral Pulse Wave Velocity in Patients Receiving Maintenance Hemodialysis.Medical science monitor : international medical journal of experimental and clinical research · 2026
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  14. The physiological effects of APOE genotype in healthy young/middle-aged individuals.Biological reviews of the Cambridge Philosophical Society · 2026
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7 more citing papers are in PubMed but not listed here.

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.

Scott T ChiesaInstitute of Cardiovascular Science University College London UK.ORCID 0000-0003-4323-2189
Marietta CharakidaDepartment of Imaging Science and Biomedical Engineering King's College London UK.
Georgios GeorgiopoulosDepartment of Imaging Science and Biomedical Engineering King's College London UK.
Justin D RobertsCambridge Centre for Sport and Exercise Sciences Anglia Ruskin University Cambridge UK.
Simon J StaffordMolecular Diagnostics Unit Medical Technology Research Centre Faculty of Health, Education, Medicine & Social Care Anglia Ruskin University Chelmsford UK.
Chloe ParkCardiometabolic Phenotyping Group Institute of Cardiovascular Science University College London UK.
Juha MykkänenResearch Centre of Applied and Preventive Cardiovascular Medicine University of Turku Finland.
Mika KähönenDepartment of Clinical Physiology Tampere University Hospital Tampere Finland.
Terho LehtimäkiFinnish Cardiovascular Research Center Tampere Faculty of Medicine and Health Technology Tampere University Tampere Finland.
Mika Ala-KorpelaComputational Medicine Faculty of Medicine University of Oulu and Biocenter Oulu Finland.
Olli RaitakariResearch Centre of Applied and Preventive Cardiovascular Medicine University of Turku Finland.
Milla PietiäinenOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.
Pirkko PussinenOral and Maxillofacial Diseases University of Helsinki and Helsinki University Hospital Helsinki Finland.ORCID 0000-0003-3563-1876
Vivek MuthuranguCentre for Cardiovascular Imaging UCL Institute of Cardiovascular Science London United Kingdom.
Alun D HughesCardiometabolic Phenotyping Group Institute of Cardiovascular Science University College London UK.ORCID 0000-0001-5432-5271
Naveed SattarInstitute of Cardiovascular and Medical Sciences British Heart Foundation (BHF) Glasgow Cardiovascular Research CentreUniversity of Glasgow UK.ORCID 0000-0002-1604-2593
Nicholas J TimpsonPopulation Health Sciences Bristol Medical School Faculty of Health Sciences University of Bristol UK.
John E DeanfieldInstitute of Cardiovascular Science University College London UK.

Funding

Maternal overnutrition and offspring fat mass, metabolic and vascular function.R01DK077659 · NIDDK · UNIVERSITY OF BRISTOL · PI LAWLOR, DEBORAH ANNE · 2006 to 2009
$986k
British Heart Foundation CS/15/6/31468British Heart Foundation PG/18/45/33814Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_19009NIDDK NIH HHS R01 DK077659Wellcome TrustWellcome Trust 076467/Z/05/ZWellcome Trust 217065/Z/19/Z
6 · The paper itself

Abstract

Background Low-grade inflammation in the young may contribute to the early development of cardiovascular disease. We assessed whether circulating levels of glycoprotein acetyls (GlycA) were better able to predict the development of adverse cardiovascular disease risk profiles compared with the more commonly used biomarker high-sensitivity CRP (C-reactive protein). Methods and Results A total of 3306 adolescents and young adults from the Avon Longitudinal Study of Parents and Children (mean age, 15.4±0.3; n=1750) and Cardiovascular Risk in Young Finns Study (mean age, 32.1±5.0; n=1556) were included. Baseline associations between inflammatory biomarkers, body composition, cardiovascular risk factors, and subclinical measures of vascular dysfunction were assessed cross-sectionally in both cohorts. Prospective risk of developing hypertension and metabolic syndrome during 9-to-10-year follow-up were also assessed as surrogate markers for future cardiovascular risk. GlycA showed greater within-subject correlation over 9-to-10-year follow-up in both cohorts compared with CRP, particularly in the younger adolescent group (r=0.36 versus 0.07). In multivariable analyses, GlycA was found to associate with multiple lifestyle-related cardiovascular disease risk factors, cardiometabolic risk factor burden, and vascular dysfunction (eg, mean difference in flow-mediated dilation=-1.2 [-1.8, -0.7]% per z-score increase). In contrast, CRP levels appeared predominantly driven by body mass index and showed little relationship to any measured cardiovascular risk factors or phenotypes. In both cohorts, only GlycA predicted future risk of both hypertension (risk ratio [RR], ≈1.1 per z-score increase for both cohorts) and metabolic syndrome (RR, ≈1.2-1.3 per z-score increase for both cohorts) in 9-to-10-year follow-up. Conclusions Low-grade inflammation captured by the novel biomarker GlycA is associated with adverse cardiovascular risk profiles from as early as adolescence and predicts future risk of hypertension and metabolic syndrome in up to 10-year follow-up. GlycA is a stable inflammatory biomarker which may capture distinct sources of inflammation in the young and may provide a more sensitive measure than CRP for detecting early cardiovascular risk.

Indexed as

Cardiovascular DiseasesHypertensionMetabolic SyndromeAdolescentBiomarkersC-Reactive ProteinGlycoproteinsHeart Disease Risk FactorsHumansInflammationLongitudinal StudiesProspective StudiesRisk FactorsBiomarkersC-Reactive ProteinGlycoproteinsALSPACcardiovascular diseaseCRPGlycAYoung Finns Study

Identifiers

PMID35156387
PMCPMC9245818

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Registered trials

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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.