Evidence map›Paper›PMID 34639156›Full record

ArticleInternational journal of molecular sciences2021

Neutrophil Pathways of Inflammation Characterize the Blood Transcriptomic Signature of Patients with Psoriasis and Cardiovascular Disease.

Amanda Kvist-Hansen, Hannah Kaiser, Xing Wang, Martin Krakauer, Peter Michael Gørtz, Benjamin D McCauley, Claus Zachariae, Christine Becker, Peter Riis Hansen, Lone Skov

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

19 citing papers in PubMed, 32 citations in OpenAlex.

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  8. Gene Expression Dysregulation in Whole Blood of Patients withInternational journal of molecular sciences · 2024
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  12. Research progress on the neutrophil components and their interactions with immune cells in the development of psoriasis.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023
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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

10 authors at 4 institutions in 2 countries.

Amanda Kvist-HansenDepartment of Dermatology and Allergy, Copenhagen University Hospital-Herlev and Gentofte, 2900 Hellerup, Denmark.ORCID 0000-0002-0390-9151
Hannah KaiserDepartment of Dermatology and Allergy, Copenhagen University Hospital-Herlev and Gentofte, 2900 Hellerup, Denmark.
Xing WangDepartment of Medicine, Division of Clinical Immunology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Martin KrakauerDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital-Bispebjerg and Frederiksberg, 2400 Copenhagen, Denmark.ORCID 0000-0002-2191-1861
Peter Michael GørtzDepartment of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital-Herlev and Gentofte, 2900 Hellerup, Denmark.
Benjamin D McCauleyDepartment of Medicine, Division of Clinical Immunology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Claus ZachariaeDepartment of Dermatology and Allergy, Copenhagen University Hospital-Herlev and Gentofte, 2900 Hellerup, Denmark.ORCID 0000-0001-5506-1319
Christine BeckerDepartment of Medicine, Division of Clinical Immunology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Peter Riis HansenDepartment of Cardiology, Copenhagen University Hospital-Herlev and Gentofte, 2900 Hellerup, Denmark.ORCID 0000-0002-9056-535X
Lone SkovDepartment of Dermatology and Allergy, Copenhagen University Hospital-Herlev and Gentofte, 2900 Hellerup, Denmark.ORCID 0000-0002-4784-9680
Gentofte Hospital · DKIcahn School of Medicine at Mount Sinai · USUniversity of Copenhagen · DKFrederiksberg Hospital · DK

Funding

LEO Foundation LF16115
6 · The paper itself

Abstract

backgroundPatients with psoriasis have an increased risk of atherosclerotic cardiovascular disease (CVD). The molecular mechanisms behind this connection are not fully understood, but the involvement of neutrophils have drawn attention as a shared inflammatory factor.

methodsRNA sequencing using the Illumina platform was performed on blood from 38 patients with moderate to severe psoriasis; approximately half had prior CVD. The neutrophil to lymphocyte ratio (NLR) was obtained from blood samples. Subclinical atherosclerosis was assessed by

results291 genes were differentially expressed between patients with psoriasis with and without CVD. These included 208 upregulated and 83 downregulated DEGs. Neutrophil degranulation was identified as the most significant process related to the upregulated DEGs. Genes for the neutrophil-associated markers MPO, MMP9, LCN2, CEACAM1, CEACAM6 and CEACAM8 were identified as being of special interest and their mRNA levels correlated with NLR, high-sensitive C-reactive protein and markers of subclinical CVD.

conclusionsPatients with psoriasis and CVD had an increased expression of genes related to neutrophil degranulation in their blood transcriptome compared with patients with psoriasis without CVD. NLR may be a potential biomarker of subclinical CVD in psoriasis.

Indexed as

TranscriptomeBiomarkersCardiovascular DiseasesFemaleHumansInflammationMaleMiddle AgedNeutrophil ActivationNeutrophilsPrognosisPsoriasisSequence Analysis, RNABiomarkerscardiovascular diseaseneutrophilsneutrophil to lymphocyte ratiopsoriasisRNA sequencingsubclinical atherosclerosistranscriptome

Identifiers

PMID34639156
PMCPMC8509817
OpenAlexW3202212228

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.