Evidence map›Paper›PMID 39639643›Full record

ReviewExpert reviews in molecular medicine2024

Unlocking the potential of miRNAs in detecting pulmonary tuberculosis: prospects and pitfalls.

Rakesh Arya, Surendra Kumar, Joseph M Vinetz, Jong Joo Kim, Reetika Chaurasia

Abstract readReview
In one paragraph

Review in Expert reviews in molecular medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Silymarin Reduces the Inflammatory Response and the Burden ofInternational journal of microbiology · 2026
    Article
  5. Article
  6. 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

5 authors.

Rakesh AryaDepartment of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk, South Korea.ORCID 0000-0003-2089-0891
Surendra KumarDepartment of Orthopaedic Surgery, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.ORCID 0009-0009-1596-8835
Joseph M VinetzDepartment of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0001-8344-2004
Jong Joo KimDepartment of Biotechnology, Yeungnam University, Gyeongsan, Gyeongbuk, South Korea.ORCID 0000-0001-9687-0075
Reetika ChaurasiaDepartment of Internal Medicine, Section of Infectious Diseases, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0002-7718-4720

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tuberculosis (TB) is one of the deadliest infectious diseases globally, ranking as 13th leading cause of mortality and morbidity. According to the Global Tuberculosis Report 2022, TB claimed the lives of 1.6 million people worldwide in 2021. Among the casualties, 1 870 000 individuals with HIV co-infections contributed to 6.7% of the total fatalities, accounting TB as the second most lethal infectious disease following COVID-19. In the quest to identify biomarkers for disease progression and anti-TB therapy, microRNAs (miRNAs) have gained attention due to their precise regulatory role in gene expression in disease stages and their ability to distinguish latent and active TB, enabling the development of early TB prognostic signatures. miRNAs are stable in biological fluids and therefore will be useful for non-invasive and broad sample collection. However, their inherent lack of specificity and experimental variations may lead to false-positive outcomes. These limitations can be overcome by integrating standard protocols with machine learning, presenting a novel tool for TB diagnostics and therapeutics. This review summarizes, discusses and highlights the potential of miRNAs as a biomarker, particularly their differential expression at disease stages. The review assesses the advantages and obstacles associated with miRNA-based diagnostic biomarkers in pulmonary TB and facilitates rapid, point-of-care testing.

Indexed as

BiomarkersMicroRNAsTuberculosis, PulmonaryCOVID-19HumansSARS-CoV-2BiomarkersMicroRNAsmiRNAmiRNA diagnostic markerMycobacterium tuberculosispulmonary tuberculosis

Identifiers

PMID39639643
PMCPMC11629464

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.