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

Publication date: Dec 06, 2024

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.

Concepts Keywords
Deadliest Biomarkers
Learning Biomarkers
Micrornas COVID-19
Tuberculosis Humans
MicroRNAs
MicroRNAs
miRNA
miRNA diagnostic marker
Mycobacterium tuberculosis
pulmonary tuberculosis
SARS-CoV-2
Tuberculosis, Pulmonary

Semantics

Type Source Name
disease MESH pulmonary tuberculosis
disease MESH Tuberculosis
pathway KEGG Tuberculosis
disease MESH infectious diseases
disease MESH morbidity
disease MESH co-infections
pathway REACTOME Infectious disease
disease IDO infectious disease
disease MESH COVID-19
disease MESH disease progression
disease IDO role

Original Article

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