Evidence map›Paper›PMID 36478058›Full record

ReviewEuropean heart journal2023

Translational opportunities of single-cell biology in atherosclerosis.

Menno P J de Winther, Magnus Bäck, Paul Evans, Delphine Gomez, Isabel Goncalves, Helle F Jørgensen, Rory R Koenen, Esther Lutgens, Giuseppe Danilo Norata, Elena Osto and 7 more

Abstract readReview
In one paragraph

Review in European heart journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

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  13. Research progress on macrophage regulation of atherosclerosis.Frontiers in cardiovascular medicine · 2026
    Review
  14. Review
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Menno P J de WintherDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam Infection and Immunity, Amsterdam UMC location University of Amsterdam, Meibergdreef 9, 1105AZ Amsterdam, The Netherlands.ORCID 0000-0002-4038-6636
Magnus BäckTranslational Cardiology, Karolinska Institute and Karolinska University Hospital, Stockholm, Sweden.ORCID 0000-0003-0853-5141
Paul EvansDepartment of Infection, Immunity and Cardiovascular Disease, INSIGNEO Institute, and the Bateson Centre, University of Sheffield, Sheffield, UK.ORCID 0000-0001-7975-681X
Delphine GomezDepartment of Medicine, Division of Cardiology, Heart, Lung, Blood and Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA, USA.ORCID 0000-0002-3880-6961
Isabel GoncalvesCardiovascular Research Translational Studies, Clinical Sciences, Lund University, Malmö, Sweden.ORCID 0000-0002-2935-0181
Helle F JørgensenCardiorespiratory Medicine Section, Department of Medicine, University of Cambridge, Hills Road, Cambridge CB2 0QQ, UK.ORCID 0000-0002-7909-2977
Rory R KoenenDepartment of Biochemistry, Cardiovascular Research Institute Maastricht, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-9955-9730
Esther LutgensInstitute of Cardiovascular Prevention (IPEK), Ludwig-Maximilian's Universität, Munich, Germany.ORCID 0000-0002-2609-5744
Giuseppe Danilo NorataDepartment of Excellence in Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy.ORCID 0000-0002-6081-1257
Elena OstoInstitute of Clinical Chemistry and Department of Cardiology, Heart Center, University Hospital and University of Zurich, Zurich, Switzerland.ORCID 0000-0001-8196-5696
Lea DibKennedy Institute of Rheumatology, NDORMS, University of Oxford, Roosevelt Drive, OX37FY Oxford, UK.ORCID 0000-0001-5889-4738
Michael SimonsDepartments of Internal Medicine and Cell Biology, Yale University and Yale Cardiovascular Research Center, 300 George St, New Haven, CT 06511, USA.ORCID 0000-0003-0348-7734
Konstantinos StellosEuropean Center for Angioscience, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID 0000-0002-0194-0825
Seppo Ylä-HerttualaA.I. Virtanen Institute, University of Eastern Finland and Heart Center, Kuopio University Hospital, Kuopio, Finland.ORCID 0000-0001-7593-2708
Holger WinkelsDepartment of Internal Medicine III, Division of Cardiology, University of Cologne, Faculty of Medicine and University Hospital Cologne, Kerpener Str. 62, 50937 Cologne, Germany.ORCID 0000-0003-1333-2031
Marie-Luce Bochaton-PiallatDepartment of Pathology and Immunology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID 0000-0001-8408-8932
Claudia MonacoKennedy Institute of Rheumatology, NDORMS, University of Oxford, Roosevelt Drive, OX37FY Oxford, UK.ORCID 0000-0003-1985-4914

Funding

Surgery / Physiology CoreP01HL107205 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL · 2012 to 2022
$18.8M
Epigenetic control of smooth muscle cell phenotype during microvascular remodelingR01HL146465 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Delphine Gomez · 2019 to 2026
$3.4M
Vascular smooth muscle cell heterogeneity and diseaseR01HL152197 · NHLBI · YALE UNIVERSITY · PI SIMONS, MICHAEL, TELLIDES, GEORGE · 2021 to 2024
$3.3M
British Heart Foundation RG/19/10/34506Medical Research Council MR/W00366X/1NHLBI NIH HHS P01 HL107205NHLBI NIH HHS R01 HL146465NHLBI NIH HHS R01 HL152197
6 · The paper itself

Abstract

The advent of single-cell biology opens a new chapter for understanding human biological processes and for diagnosing, monitoring, and treating disease. This revolution now reaches the field of cardiovascular disease (CVD). New technologies to interrogate CVD samples at single-cell resolution are allowing the identification of novel cell communities that are important in shaping disease development and direct towards new therapeutic strategies. These approaches have begun to revolutionize atherosclerosis pathology and redraw our understanding of disease development. This review discusses the state-of-the-art of single-cell analysis of atherosclerotic plaques, with a particular focus on human lesions, and presents the current resolution of cellular subpopulations and their heterogeneity and plasticity in relation to clinically relevant features. Opportunities and pitfalls of current technologies as well as the clinical impact of single-cell technologies in CVD patient care are highlighted, advocating for multidisciplinary and international collaborative efforts to join the cellular dots of CVD.

Indexed as

AtherosclerosisCardiovascular DiseasesPlaque, AtheroscleroticHumansAtherosclerosisEndothelial cellLymphocyteMacrophageSingle-cell biologySmooth muscle cell

Identifiers

PMID36478058
PMCPMC10120164

What OpenQuestion holds

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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.