# The Role of microRNAs and Cell-Free DNAs in Fungal Infections: Systematic Review and Meta-Analysis of the Literature

**Authors:** Ayse Kalkanci, Fatma Bozdag, Isil Fidan, Ozlem Guzel Tunccan, Sultan Pinar Cetintepe, Mustafa Necmi Ilhan

PMC · DOI: 10.3390/jof11100718 · Journal of Fungi · 2025-10-04

## TL;DR

This paper reviews how microRNAs and cell-free DNA can help diagnose and monitor fungal infections in patients with weakened immune systems.

## Contribution

The study systematically evaluates the diagnostic and prognostic potential of cfDNA and miRNAs in fungal infections using a meta-analysis and literature review.

## Key findings

- Cell-free DNA positivity was observed in 79% of patients with proven fungal infections.
- miRNAs like miR-132 and miR-146a showed high diagnostic accuracy and prognostic value.

## Abstract

Background: Invasive fungal infections (IFIs) remain a major cause of morbidity and mortality among immunocompromised patients, despite advances in antifungal therapy. Conventional diagnostics are limited, highlighting the need for novel biomarkers. Circulating microRNAs (miRNAs) and cell-free DNA (cfDNA) have emerged as promising tools due to their roles in immune regulation, pathogen–host interactions, and disease monitoring. This systematic review and meta-analysis evaluate their diagnostic and prognostic potential in fungal infections. Methods: A systematic search of PubMed, Web of Science, SCOPUS, and EMBASE was conducted up to May 2025 in line with PRISMA guidelines (PROSPERO protocol CRD42021287150). Eligible studies included clinical research on confirmed fungal infections assessing cfDNA or miRNAs. Random-effects meta-analyses were performed for cfDNA, and miRNA findings were synthesized descriptively. Results: In total, 526 studies were included. cfDNA positivity was observed in 12% of all tested samples (95% CI: 0.06–0.22) and in 79% of patients with proven fungal infections (95% CI: 0.62–0.90), supporting its value as a minimally invasive, culture-independent diagnostic marker. Six studies on miRNAs identified disease-specific signatures, including miR-132 and miRNA panels for aspergillosis, with high diagnostic accuracy (AUC ≥ 0.98). miR-146a, miR-223, and miR-545 further correlated with prognosis and mortality. Conclusions: cfDNA and miRNAs show strong potential for early diagnosis, prognosis, and treatment monitoring in IFIs. Standardized methodologies and large-scale validation are essential for clinical translation.

## Linked entities

- **Diseases:** aspergillosis (MONDO:0005657)

## Full-text entities

- **Genes:** MIR146A (microRNA 146a) [NCBI Gene 406938] {aka MIRN146, MIRN146A, miR-146a, miRNA146A}, MIR223 (microRNA 223) [NCBI Gene 407008] {aka MIRN223, miRNA223, mir-223}, MIR545 (microRNA 545) [NCBI Gene 664614] {aka MIRN545, hsa-mir-545, mir-545}, MIR132 (microRNA 132) [NCBI Gene 406921] {aka MIRN132, miRNA132, mir-132}
- **Diseases:** Fungal Infections (MESH:D009181), aspergillosis (MESH:D001228), IFIs (MESH:D000072742)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12565099/full.md

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Source: https://tomesphere.com/paper/PMC12565099