Evidence map›Paper›PMID 41009639›Full record

ArticleInternational journal of molecular sciences2025

Comprehensive Profiling Identifies Circulating microRNA Dysregulation in Vietnamese Patients with Heart Failure.

Bao-Quoc Vu, Phuong Anh Huynh, Nhu Nhat Quynh Nguyen, Niem Van Thanh Vo, Linh Gia Hoang Le, Vu Hoang Vu, Thanh Cong Nguyen, Minh Hoang, Diem My Vu

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Plasma Expression andBiomolecules · 2026
    Article
  3. Article
  4. Review
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.

Bao-Quoc VuCenter for Molecular Biomedicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0000-0002-2491-9682
Phuong Anh HuynhCenter for Molecular Biomedicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0009-0001-9032-840X
Nhu Nhat Quynh NguyenCenter for Molecular Biomedicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0000-0003-0782-4312
Niem Van Thanh VoCenter for Molecular Biomedicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0000-0002-9089-5199
Linh Gia Hoang LeCenter for Molecular Biomedicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0009-0006-6310-4845
Vu Hoang VuDepartment of Internal Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0000-0001-5482-859X
Thanh Cong NguyenCardiovascular Center, University Medical Center Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.
Minh HoangPasteur Institute of Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.ORCID 0000-0002-3444-1360
Diem My VuCenter for Molecular Biomedicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Vietnam.

Funding

This work has received support from the Korea International Cooperation Agency (KOICA) under the project entitled "Education and Research Capacity Building Project at University of Medicine and Pharmacy at Ho Chi Minh City", conducted from 2024 to 2025 2021-00020-3
6 · The paper itself

Abstract

Heart failure (HF) is a complex and multifactorial syndrome with high morbidity and mortality rates worldwide. Accumulative evidence suggests that microRNAs (miRNAs) play critical roles in maintaining cardiac homeostasis. The dysregulation of various miRNAs has been reported in different studies on failing human hearts. However, little is known about their circulatory profile. In this study, comprehensive miRNA profiling was performed by next-generation sequencing for plasma samples of 24 HF and 24 age and sex-matched, non-HF patients. A total of 1391 miRNAs were detected, of which 228 miRNAs and 261 miRNAs were commonly expressed in the HF and non-HF groups, respectively. Eight miRNAs (hsa-let-7b-3p, hsa-miR-92b-5p, hsa-miR-145-3p, hsa-miR-206, hsa-miR-664a-5p, hsa-miR-1307-5p, hsa-miR-1908-5p, and hsa-miR-3074-5p) were found to be dysregulated between HF and non-HF patients. The expression of another seven miRNAs (hsa-miR-589-5p, hsa-miR-30b-5p, hsa-miR-654-3p, hsa-miR-1292-5p, hsa-miR-659-5p, hsa-miR-548d-5p, and hsa-miR-7847-3p) was frequently observed in HF patients but not in non-HF cases. Subsequent analyses of target gene prediction and associated pathways revealed the enrichment of pathways related to vascular development, the cell cycle, and transcriptional activity. These data reveal the expression profile and the dysregulation of circulating miRNAs in our patients with HF.

Indexed as

Circulating MicroRNAHeart FailureMicroRNAsAgedBiomarkersCase-Control StudiesFemaleGene Expression ProfilingGene Expression RegulationHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedSoutheast Asian PeopleVietnamBiomarkersCirculating MicroRNAMicroRNAscirculating miRNAsheart failurenext generation sequencing

Identifiers

PMID41009639
PMCPMC12470235

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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.