Evidence map›Paper›PMID 39633383›Full record

ArticleCardiovascular diabetology2024

ApoC-III proteoforms are associated with better lipid, inflammatory, and glucose profiles independent of total apoC-III.

Pere Rehues, Josefa Girona, Montse Guardiola, Enrique Ozcariz, Núria Amigó, Roser Rosales, Yaiza Esteban, Helena Banús, Gemma Gavaldà-Alsina, Ana González-Lleó and 2 more

Abstract readComparative Study
In one paragraph

Article in Cardiovascular diabetology, 2024. 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
–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

3 citing papers in PubMed.

  1. Review
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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

12 authors.

Pere Rehues *Unitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Josefa Girona *Unitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Montse GuardiolaUnitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain. montse.guardiola@urv.cat.
Enrique OzcarizCenter for Health and Bioresources, Molecular Diagnostics, AIT Austrian Institute of Technology GmbH, Vienna, Austria.
Núria AmigóInstitut d'Investigació Sanitària Pere Virgili, Reus, Spain.
Roser RosalesUnitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Yaiza EstebanUnitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Helena BanúsUnitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Gemma Gavaldà-AlsinaUnitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Ana González-LleóUnitat de Medicina Vascular i Metabolisme. Servei de Medicina Interna, Hospital Universitari Sant Joan de Reus, Reus, Spain.
Gemma Rojo-MartínezCentro de Investigación Biomédica en Red de Diabetes y Enfermedades Metabólicas Asociadas, Madrid, Spain.
Josep RibaltaUnitat de Recerca en Lípids i Arteriosclerosi, Departament de Medicina i Cirurgia, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.

Funding

Instituto de Salud Carlos III PI21/01294Ministerio de Universidades FPU19/04610
6 · The paper itself

Abstract

backgroundApolipoprotein (apo) C-III is involved in several processes that increase triglyceride levels, inflammation, and insulin resistance. Four of its proteoforms have been the focus of several studies and have shown differential associations with cardiovascular risk biomarkers, mostly lipids. However, there are other proteoforms of apoC-III that have not yet been investigated in detail. The aim of this study was to evaluate the associations of seven apoC-III proteoforms with a comprehensive set of biomarkers, including lipid metabolism, inflammation, and glucose homeostasis.

methodsSeven apoC-III proteoforms (apoC-III

resultsThree proteoform ratios (apoC-III

conclusionsWhile apoC-III is positively associated with biomarkers of cardiometabolic risk, the proportions of three apoC-III proteoforms show opposite associations, independent of total apoC-III concentrations. Measuring not only apoC-III but also the proportions of apoC-III proteoforms can provide valuable information since individuals with similar levels of total apoC-III could display opposite lipid profiles depending on the proportion of apoC-III proteoforms.

Indexed as

Apolipoprotein C-IIIBiomarkersBlood GlucoseInflammationInflammation MediatorsAdultAgedCross-Sectional StudiesFemaleHumansInsulin ResistanceLipidsMaleMiddle AgedRisk AssessmentAPOC3 protein, humanApolipoprotein C-IIIBiomarkersBlood GlucoseInflammation MediatorsLipidsApolipoprotein C-IIICardiovascular diseaseDyslipidemiaGlycoproteinsInflammationInsulin resistanceLipoproteinsProteoformsTriglyceridesType 2 diabetes

Identifiers

PMID39633383
PMCPMC11619673

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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.