Evidence map›Paper›PMID 38211336›Full record

ArticleBlood2024

High microRNA-145 plasma levels are associated with decreased risk of future incident venous thromboembolism: the HUNT study.

Vânia M Morelli, Omri Snir, Kristian Dalsbø Hindberg, Kristian Hveem, Sigrid K Brækkan, John-Bjarne Hansen

Abstract read
PubMed Publisher
In one paragraph

Article in Blood, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Plasma microRNA-145-5p as a diagnostic biomarker for acute deep vein thrombosis.Research and practice in thrombosis and haemostasis · 2025
    Article
  8. Review
  9. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Vânia M MorelliThrombosis Research Group, Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0002-0872-6645
Omri SnirThrombosis Research Group, Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway.
Kristian Dalsbø HindbergThrombosis Research Center, Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway.ORCID 0000-0002-8194-6679
Kristian HveemK. G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Levanger, Norway.
Sigrid K BrækkanThrombosis Research Group, Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0002-9678-9696
John-Bjarne HansenThrombosis Research Group, Department of Clinical Medicine, UiT The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0003-4854-3162
University Hospital of North Norway · NONorwegian University of Science and Technology · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractMicroRNA-145 (miR-145) has been reported to downregulate the expression of tissue factor and factor XI in vitro and decrease venous thrombus formation in animal models. However, the association between miR-145 and risk of future venous thromboembolism (VTE) in the general population remains unknown. We investigated the association between plasma levels of miR-145 and risk of future VTE in a case-cohort study. Incident VTE cases (n = 510) and a subcohort (n = 1890) were derived from the third survey of the Trøndelag Health Study (HUNT3), a population-based cohort. The expression levels of miR-145 were measured in plasma samples obtained at baseline. The study population was divided into quartiles based on miR-145 levels in participants in the subcohort, and weighted Cox regression was used to estimate hazard ratios (HRs) with 95% confidence intervals (CIs). Plasma levels of miR-145 were inversely associated with VTE risk. Participants with miR-145 levels in the highest quartile had a 49% lower risk of VTE (HR, 0.51; 95% CI, 0.38-0.68) than those with miR-145 in the lowest quartile in age- and sex-adjusted analysis, and the inverse association was most pronounced for unprovoked VTE (HR, 0.39; 95% CI, 0.25-0.61). Risk estimates remained virtually the same after further adjustment for body mass index, and cancer and arterial cardiovascular disease at baseline. In conclusion, elevated expression levels of miR-145 in plasma were associated with decreased risk of future incident VTE. The protective role of miR-145 against VTE is consistent with previous experimental data and suggests that miR-145 has the potential to be a target for VTE prevention.

Indexed as

MicroRNAsVenous ThromboembolismAdultAgedCase-Control StudiesCohort StudiesFemaleHumansIncidenceMaleMiddle AgedNorwayRisk FactorsMicroRNAsMIRN145 microRNA, human

Identifiers

PMID38211336
OpenAlexW4390731820

What OpenQuestion holds

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Registered trials

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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.