Evidence map›Paper›PMID 40701821›Full record

Observational studyBritish journal of haematology2025

Prevalence and impact of additional CHIP mutations in JAK2V617F-positive ischaemic cerebrovascular patients.

Marie Hvelplund Kristiansen, Vibe Skov, Morten Kranker Larsen, Lasse Kjær, Claus Henrik Nielsen, Hans Carl Hasselbalch, Troels Wienecke

Abstract readObservational Study
In one paragraph

Observational study in British journal of haematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Observational
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

7 authors.

Marie Hvelplund KristiansenDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-4285-6766
Vibe SkovDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.ORCID https://orcid.org/0000-0003-0097-7826
Morten Kranker LarsenDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0002-2873-5928
Lasse KjærDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.ORCID https://orcid.org/0000-0001-6767-0226
Claus Henrik NielsenSection for Oral Biology and Immunopathology, Department of Odontology, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Hans Carl HasselbalchDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.ORCID https://orcid.org/0000-0003-3936-8032
Troels WieneckeDepartment of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

Funding

Fabrikant Einar Willumsens MindelegatFonden til Lægevidenskabens FremmeGreater Copenhagen Health Science PartnersGrosserer A.V. Lykfeldt og Hustrus LegatHarboefondenRegion Sjællands Sundhedsvidenskabelige ForskningsfondSnedkermester Sophus Jacobsen og Hustru Astrid Jacobsens FondToyota-Fonden
6 · The paper itself

Abstract

The JAK2V617F mutation is associated with increased cardiovascular risk, including ischaemic stroke. This study investigates the prevalence of additional mutations in ischaemic cerebrovascular patients with and without JAK2V617F to better understand the mechanisms contributing to thrombotic risk. We examined 63 patients with the JAK2V617F mutation and 126 matched controls from a cohort of 591 ischaemic cerebrovascular patients. Somatic mutations were assessed using targeted next-generation sequencing (NGS). Serum thromboinflammatory markers were evaluated in a subset of patients. Additional somatic mutations were more common in JAK2V617F-positive patients than in controls (47.6% vs. 30.2%, p = 0.028). Patients with JAK2V617F had a higher prevalence of other mutations with variant allele frequencies (VAFs) above 10% (23.8% vs. 7.9%, p = 0.005), a pattern that persisted in cases with JAK2V617F <1% (p = 0.019). In JAK2V617F-positive patients, additional somatic mutations were associated with higher monocyte levels, even when excluding myeloproliferative neoplasms patients (p = 0.011). Patients with other clonal haematopoiesis of indeterminate potential mutations exhibited higher vascular cell adhesion molecule 1 (p = 0.027), soluble urokinase plasminogen activator receptor (p = 0.010) and IL-10 (p = 0.045), as well as higher neutrophil to lymphocyte ratio (p = 0.002). Ischaemic cerebrovascular patients with the JAK2V617F mutation more frequently harbour other somatic mutations and at higher VAF. This may reflect a more advanced clonal profile with relevance for vascular risk in JAK2V617F-positive individuals.

Indexed as

Ischemic Attack, TransientIschemic StrokeJanus Kinase 2Retinal Artery OcclusionUbiquitin-Protein LigasesAgedAged, 80 and overDenmarkFemaleGene FrequencyHumansLeukocyte CountMaleMiddle AgedMonocytesMutationJAK2 protein, humanJanus Kinase 2STUB1 protein, humanUbiquitin-Protein Ligaseshaematopoiesismolecular geneticsthrombosis

Identifiers

PMID40701821
PMCPMC12436222

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.