Evidence map›Paper›PMID 37317065›Full record

ArticleJournal of cellular and molecular medicine2023

RNA sequencing suggests that non-coding RNAs play a role in the development of acquired haemophilia.

Adrian Bogdan Tigu, Ionut Hotea, Rares Drula, Alina-Andreea Zimta, Noemi Dirzu, Maria Santa, Catalin Constantinescu, Delia Dima, Jon Thor Bergthorsson, Victor Greiff and 5 more

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. 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. Article
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

15 authors.

Adrian Bogdan TiguMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Ionut HoteaDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Rares DrulaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Alina-Andreea ZimtaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Noemi DirzuMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Maria SantaDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Catalin ConstantinescuDepartment of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Delia DimaDepartment of Hematology, Ion Chiricuta Clinical Cancer Center, Cluj Napoca, Romania.
Jon Thor BergthorssonBiomedical Center, School of Health Sciences, University of Iceland, Reykjavík, Iceland.
Victor GreiffDepartment of Immunology, University of Oslo and Oslo University Hospital, Oslo, Norway.
Diana GuleiMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.
Daniel CoriuDepartment of Hematology, Carol Davila University of Medicine and Pharmacy, Cluj Napoca, Romania.ORCID 0000-0002-7251-6079
Margit SerbanDepartment of Pediatrics, Victor Babes University of Medicine and Pharmacy, Timisoara, Romania.
Johnny MahlanguHaemophilia Comprehensive Care Centre, Charlotte Maxeke Johannesburg Academic Hospital, University of the Witwatersrand and National Health Laboratory Service, Johannesburg, South Africa.
Ciprian TomuleasaMedfuture Research Center for Advanced Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj Napoca, Romania.ORCID 0000-0001-5500-1519

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acquired haemophilia (AH) is a rare disorder characterized by bleeding in patients with no personal or family history of coagulation/clotting-related diseases. This disease occurs when the immune system, by mistake, generates autoantibodies that target FVIII, causing bleeding. Small RNAs from plasma collected from AH patients (n = 2), mild classical haemophilia (n = 3), severe classical haemophilia (n = 3) and healthy donors (n = 2), for sequencing by Illumina, NextSeq500. Based on bioinformatic analysis, AH patients were compared to all experimental groups and a significant number of altered transcripts were identified with one transcript being modified compared to all groups at fold change level. The Venn diagram shows that haemoglobin subunit alpha 1 was highlighted to be the common upregulated transcript in AH compared to classical haemophilia and healthy patients. Non-coding RNAs might play a role in AH pathogenesis; however, due to the rarity of HA, the current study needs to be translated on a larger number of AH samples and classical haemophilia samples to generate more solid data that can confirm our findings.

Indexed as

Hemophilia AFactor VIIIHemorrhageHumansRNA, UntranslatedSequence Analysis, RNAFactor VIIIRNA, Untranslatedacquired haemophiliacoagulationepigeneticsfactor VIIIRNA sequencing

Identifiers

PMID37317065
PMCPMC10315746

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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.