Evidence map›Paper›PMID 35409153›Full record

ArticleInternational journal of molecular sciences2022

Circulating miR-499a-5p Is a Potential Biomarker of

Natalia Baulina, Maria Pisklova, Ivan Kiselev, Olga Chumakova, Dmitry Zateyshchikov, Olga Favorova

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. MYH7 in cardiomyopathy and skeletal muscle myopathy.Molecular and cellular biochemistry · 2024
    Review
  9. Review
  10. Review
  11. Many Faces of Next-Generation Sequencing in Gene Expression Studies.International journal of molecular sciences · 2023
    Article
  12. Review
  13. Article
  14. Article
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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

6 authors at 3 institutions in 1 country.

Natalia BaulinaNational Medical Research Center for Cardiology, Laboratory of Functional Genomics of Cardiovascular Diseases, 121552 Moscow, Russia.ORCID 0000-0001-8767-2958
Maria PisklovaNational Medical Research Center for Cardiology, Laboratory of Functional Genomics of Cardiovascular Diseases, 121552 Moscow, Russia.
Ivan KiselevNational Medical Research Center for Cardiology, Laboratory of Functional Genomics of Cardiovascular Diseases, 121552 Moscow, Russia.ORCID 0000-0003-3366-4113
Olga ChumakovaNational Medical Research Center for Cardiology, Laboratory of Functional Genomics of Cardiovascular Diseases, 121552 Moscow, Russia.ORCID 0000-0003-2373-1183
Dmitry ZateyshchikovNational Medical Research Center for Cardiology, Laboratory of Functional Genomics of Cardiovascular Diseases, 121552 Moscow, Russia.ORCID 0000-0001-7065-2045
Olga FavorovaNational Medical Research Center for Cardiology, Laboratory of Functional Genomics of Cardiovascular Diseases, 121552 Moscow, Russia.
Pirogov Russian National Research Medical University · RUCity Clinical Hospital · RUNational Medical Research Center of Cardiology · RU

Funding

Russian Science Foundation 20-15-00353
6 · The paper itself

Abstract

Hypertrophic cardiomyopathy (HCM) is the most common inherited myocardial disease with significant genetic and phenotypic heterogeneity. To search for novel biomarkers, which could increase the accuracy of HCM diagnosis and improve understanding of its phenotype formation, we analyzed the levels of circulating miRNAs—stable non-coding RNAs involved in post-transcriptional gene regulation. Performed high throughput sequencing of miRNAs in plasma of HCM patients and controls pinpointed miR-499a-5p as one of 35 miRNAs dysregulated in HCM. Further investigation on enlarged groups of individuals showed that its level was higher in carriers of pathogenic/likely pathogenic (P/LP) variants in MYH7 gene compared to controls (fold change, FC = 8.9; p < 0.0001). Just as important, carriers of variants in MYH7 gene were defined with higher miRNA levels than carriers of variants in the MYBPC3 gene (FC = 14.1; p = 0.0003) and other patients (FC = 4.1; p = 0.0008). The receiver operating characteristic analysis analysis showed the ability of miR-499a-5p to identify MYH7 variant carriers with the HCM phenotype with area under the curve value of 0.95 (95% confidence interval: 0.88−1.03, p = 0.0004); sensitivity and specificity were 0.86 and 0.91 (cut-off = 0.0014). Therefore, miR-499a-5p could serve as a circulating biomarker of HCM, caused by P/LP variants in MYH7 gene.

Indexed as

Cardiomyopathy, HypertrophicMicroRNAsBiomarkersCardiac MyosinsHumansMutationMyocardiumMyosin Heavy ChainsBiomarkersCardiac MyosinsMicroRNAsMYH7 protein, humanMyosin Heavy Chainsbiomarkerhypertrophic cardiomyopathymiR-499-5pmiRNAMYH7MYH7Bpathogenic genetic variantsRNA-seq

Identifiers

PMID35409153
PMCPMC8998764
OpenAlexW4221051119

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.