Evidence map›Paper›PMID 36768645›Full record

Observational studyInternational journal of molecular sciences2023

PCSK9 Inhibitors Have Apolipoprotein C-III-Related Anti-Inflammatory Activity, Assessed by 1H-NMR Glycoprotein Profile in Subjects at High or very High Cardiovascular Risk.

Pere Rehues, Josefa Girona, Montse Guardiola, Núria Plana, Roberto Scicali, Salvatore Piro, Ovidio Muñiz-Grijalvo, José Luis Díaz-Díaz, Lluís Recasens, Marta Pinyol and 6 more

Full text readObservational Study
In one paragraph

Observational study in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  6. 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

16 authors.

Pere RehuesUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.
Josefa GironaUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.ORCID 0000-0002-6267-8779
Montse GuardiolaUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.ORCID 0000-0002-9696-7384
Núria PlanaInstitut d'Investigació Sanitària Pere Virgili, 43204 Reus, Spain.
Roberto ScicaliDepartment of Clinical and Experimental Medicine, University of Catania, 95131 Catania, Italy.ORCID 0000-0002-7023-3649
Salvatore PiroDepartment of Clinical and Experimental Medicine, University of Catania, 95131 Catania, Italy.ORCID 0000-0002-1781-0902
Ovidio Muñiz-GrijalvoUnidad Clinico-Experimental de Riesgo Vascular, Hospital Virgen del Rocío, 41013 Sevilla, Spain.
José Luis Díaz-DíazDepartment of Internal Medicine, Complejo Hospitalario Universitario A Coruña, 15006 A Coruña, Spain.ORCID 0000-0002-9194-495X
Lluís RecasensHeart Diseases Biomedical Research Group, IMIM (Hospital del Mar Medical Research Institute), 08003 Barcelona, Spain.
Marta PinyolUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.
Roser RosalesUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.
Yaiza EstebanUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.
Núria AmigóInstitut d'Investigació Sanitària Pere Virgili, 43204 Reus, Spain.ORCID 0000-0002-0116-9145
Lluís MasanaUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.ORCID 0000-0002-0789-4954
Daiana IbarretxeUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.
Josep RibaltaUniversitat Rovira i Virgili, Departament de Medicina i Cirurgia, Unitat de Recerca en Lípids i Arteriosclerosi, 43201 Reus, Spain.ORCID 0000-0002-8879-4719

Funding

Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas CB07/08/0028Ministerio de Universidades, Spain FPU19/04610Ministry of Economy, Industry and Competitiveness PI21/01294Sanofi (Spain) Allied
6 · The paper itself

Abstract

Atherosclerosis is a chronic inflammatory disease caused by the accumulation of cholesterol in the intima. Proprotein convertase subtilisin/kexin type 9 inhibitors (iPCSK9) can reduce low-density lipoprotein (LDL) cholesterol levels by 60%, but there is still no evidence that they can lower markers of systemic inflammation such as high-sensitivity C-reactive protein (hsCRP). Acute-phase serum glycoproteins are upregulated in the liver during systemic inflammation, and their role as inflammatory biomarkers is under clinical evaluation. In this observational study, we evaluate the effects of iPCSK9 on glycoproteins (Glyc) A, B and F. Thirty-nine patients eligible for iPCSK9 therapy were enrolled. One sample before and after one to six months of iPCSK9 therapy with alirocumab was obtained from each patient. Lipids, apolipoproteins, hsCRP and PCSK9 levels were measured by biochemical analyses, and the lipoprotein and glycoprotein profiles were measured by 1H nuclear magnetic resonance (1H-NMR). The PCSK9 inhibitor reduced total (36.27%,

Indexed as

Cardiovascular DiseasesProprotein Convertase 9Anti-Inflammatory AgentsApolipoprotein C-IIICholesterolCholesterol, LDLC-Reactive ProteinGlycoproteinsHeart Disease Risk FactorsHumansInflammationLipoproteinsMagnetic Resonance SpectroscopyPCSK9 InhibitorsProton Magnetic Resonance SpectroscopyRisk FactorsAnti-Inflammatory AgentsApolipoprotein C-IIICholesterolCholesterol, LDLC-Reactive ProteinGlycoproteinsLipoproteinsPCSK9 InhibitorsPCSK9 protein, humanProprotein Convertase 9Triglyceridesalirocumabapolipoprotein C-IIIglycoproteinsinflammationLDLPCSK9

Identifiers

PMID36768645
PMCPMC9917120

What Socratic holds

Textfull text, public
LicenceCC BY
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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 Socratic graph.