Evidence map›Paper›PMID 41898605›Full record

ArticleInternational journal of molecular sciences2026

C-X-C Motif Chemokine Ligand 5 (CXCL5) Exhibits a U-Shaped Risk Profile for Mortality in Patients with Suspected Coronary Chest Pain.

Dennis Winston T Nilsen, Patrycja Anna Naesgaard, Volker Poenitz, Trygve Brugger-Andersen, Heidi Grundt, Annika Elisabet Michelsen, Pål Aukrust, Harry Staines, Thor Ueland

Registry-linked trialAbstract readClinical Study
In one paragraph

Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00521976 (An Investigation of Activated Factor XII), which is not on this map. Not yet cited in PubMed.

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

NCT00521976 completednot on this map

An Investigation of Activated Factor XII (Fxlla) as a Prognostic Marker.

TypeobservationalSponsorHelse Stavanger HFRan2002 to 2005Enrolled871ConditionsChest Pain, Coronary Artery Disease, Unstable Angina Pectoris, Myocardial Infarction
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Dennis Winston T NilsenDepartment of Clinical Science, University of Bergen, 5021 Bergen, Norway.ORCID 0000-0001-6142-6863
Patrycja Anna NaesgaardDepartment of Cardiology, Stavanger University Hospital, 4068 Stavanger, Norway.
Volker PoenitzDepartment of Cardiology, Stavanger University Hospital, 4068 Stavanger, Norway.
Trygve Brugger-AndersenDepartment of Cardiology, Stavanger University Hospital, 4068 Stavanger, Norway.
Heidi GrundtDepartment of Respiratory Medicine, Stavanger University Hospital, 4068 Stavanger, Norway.
Annika Elisabet MichelsenInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, 0318 Oslo, Norway.ORCID 0000-0001-7207-2407
Pål AukrustInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, 0318 Oslo, Norway.
Harry StainesSigma Statistical Services, Balmullo KY16 0BD, UK.ORCID 0000-0003-1135-5221
Thor UelandInstitute of Clinical Medicine, Faculty of Medicine, University of Oslo, 0318 Oslo, Norway.ORCID 0000-0001-5005-0784

Funding

Western Norway Regional Health Authority, Norway. N/A
6 · The paper itself

Abstract

CXCL5 is a platelet-derived chemokine which promotes inflammatory responses in neutrophils and monocytes through CXCR2. Previous studies on CXCL5 in atherogenesis are to some degree conflicting, with scarce outcome data following acute coronary syndrome. This study aimed to assess the utility and risk profile of CXCL5 as a prognostic marker of all-cause mortality at 5-year follow-up in patients hospitalized for chest pain of suspected coronary origin. We measured CXCL5 levels in platelet-poor plasma in 826 consecutive patients included in the "Risk Markers in the Acute Coronary Syndrome" (RACS) study (ClinicalTrials.gov Identifier: NCT00521976). Stepwise Cox regression models, applying quintiles, were fitted for the biomarker with all-cause mortality within 5 years as the dependent variable. At 5-year follow-up, 250 (30.3%) of the population had died; 34.5% in Quintile (Qt)-1, 32.1% in Qt-2, 23.5% in Qt-3, 29.1% in Qt-4, and 32.1% in Qt-5. Using Qt-3 as a reference, both the univariate and multivariable analysis showed a U-shaped association between CXCL5 and all-cause mortality. Univariate analysis: Qt-1 vs. Qt-3: HR 1.59 (95% CI 1.06-2.39),

Indexed as

Acute Coronary SyndromeChemokine CXCL5Chest PainAgedBiomarkersFemaleHumansMaleMiddle AgedPrognosisRisk FactorsBiomarkersChemokine CXCL5CXCL5 protein, humanacute coronary syndrome (ACS)all-cause mortalitycomposite cardiovascular event (all-cause mortality or myocardial infarction or stroke)C-X-C motif chemokine ligand 5 (CXCL5)prognostic biomarkers

Identifiers

PMID41898605
PMCPMC13026667

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Registered trials

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