Evidence map›Paper›PMID 39273602›Full record

ArticleInternational journal of molecular sciences2024

Associations between Various Inflammatory Markers and Carotid Findings in a Voluntary Asymptomatic Population Sample.

Balázs Bence Nyárády, Edit Dósa, László Kőhidai, Éva Pállinger, Renáta Gubán, Ádám Szőnyi, Loretta Zsuzsa Kiss, Zsolt Bagyura

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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. Article
  2. Article
  3. Review
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

8 authors.

Balázs Bence NyárádyHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.ORCID 0000-0003-2345-186X
Edit DósaHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
László KőhidaiDepartment of Genetics, Cell and Immunobiology, Semmelweis University, 1089 Budapest, Hungary.
Éva PállingerDepartment of Genetics, Cell and Immunobiology, Semmelweis University, 1089 Budapest, Hungary.
Renáta GubánHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Ádám SzőnyiHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Loretta Zsuzsa KissHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.
Zsolt BagyuraHeart and Vascular Center, Semmelweis University, 1122 Budapest, Hungary.ORCID 0000-0001-8120-2322

Funding

European Union RRF-2.3.1-21-2022-00003National Research, Development and Innovation Fund of Hungary EFOP-3.6.3-VEKOP-16-2017-00009National Research, Development and Innovation Fund of Hungary NKFI-146929-KNational Research, Development and Innovation Fund of Hungary NVKP_16-1-2016-0017National Research, Development and Innovation Fund of Hungary TKP2021-NVA-15
6 · The paper itself

Abstract

Cardiovascular disease (CVD) is the leading cause of morbidity and mortality worldwide, and atherosclerosis is the key factor promoting its development. Carotid intima-media thickening and the presence of carotid plaques are important indices of cardiovascular risk. In addition, inflammation is a major and complex factor in the development of atherosclerosis. The relationships between carotid atherosclerosis and certain inflammatory markers have rarely been studied in healthy individuals. Therefore, we aimed to investigate the associations between subclinical carotid atherosclerosis and various inflammatory biomarkers in a large Caucasian population free of evident CVD. In addition to recording study participants' demographic characteristics, anthropometric characteristics, and atherosclerotic risk factors, laboratory tests were performed to measure levels of hemoglobin A1c (HbA1c), high-sensitivity C-reactive protein, and inflammatory cytokines/chemokines, including interleukin (IL)-1β, IL-6, IL-8, IL-10, IL-12p70, IL-17A, IL-18, IL-23, IL-33, interferon (IFN)-α2, IFN-γ, tumor necrosis factor-α, and monocyte chemoattractant protein (MCP)-1. This study included 264 asymptomatic individuals with a median age of 61.7 years (interquartile range, 54.5-67.5 years); 45.7% of participants were male. Participants were divided into two groups according to their carotid status: the normal carotid group, comprising 120 participants; and the pathological carotid group, comprising 144 participants. Compared with the normal carotid group, hypertension and diabetes mellitus were significantly more common and serum levels of HbA1c, IL-8, and MCP-1 were significantly higher in the pathological carotid group. Multivariate regression analysis revealed significant positive associations between pathological carotid findings and serum levels of IL-8 (highest tertile, OR: 2.4,

Indexed as

BiomarkersCarotid Artery DiseasesCarotid Intima-Media ThicknessCytokinesInflammationAgedAsymptomatic DiseasesCarotid ArteriesChemokine CCL2C-Reactive ProteinFemaleGlycated HemoglobinHumansInflammation MediatorsMaleMiddle AgedBiomarkersChemokine CCL2C-Reactive ProteinCytokinesGlycated HemoglobinInflammation Mediatorsatherosclerosiscardiovascular risk factorscarotid intima-media thicknesschemokinescytokinesimmunityinflammation

Identifiers

PMID39273602
PMCPMC11394953

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.