» Articles » PMID: 38790182

Exploring the Role of Cell-Free Nucleic Acids and Peritoneal Dialysis: A Narrative Review

Overview
Journal Genes (Basel)
Publisher MDPI
Date 2024 May 25
PMID 38790182
Authors
Affiliations
Soon will be listed here.
Abstract

Introduction: Cell-free nucleic acids (cf-NAs) represent a promising biomarker of various pathological and physiological conditions. Since its discovery in 1948, cf-NAs gained prognostic value in oncology, immunology, and other relevant fields. In peritoneal dialysis (PD), blood purification is performed by exposing the peritoneal membrane. Relevant sections: Complications of PD such as acute peritonitis and peritoneal membrane aging are often critical in PD patient management. In this review, we focused on bacterial DNA, cell-free DNA, mitochondrial DNA (mtDNA), microRNA (miRNA), and their potential uses as biomarkers for monitoring PD and its complications. For instance, the isolation of bacterial DNA in early acute peritonitis allows bacterial identification and subsequent therapy implementation. Cell-free DNA in peritoneal dialysis effluent (PDE) represents a marker of stress of the peritoneal membrane in both acute and chronic PD complications. Moreover, miRNA are promising hallmarks of peritoneal membrane remodeling and aging, even before its manifestation. In this scenario, with multiple cytokines involved, mtDNA could be considered equally meaningful to determine tissue inflammation.

Conclusions: This review explores the relevance of cf-NAs in PD, demonstrating its promising role for both diagnosis and treatment. Further studies are necessary to implement the use of cf-NAs in PD clinical practice.

Citing Articles

Screening for nasal carriage of Staphylococcus (S.) aureus reduces the risk of S. aureus peritonitis in patients on peritoneal dialysis (PD).

Alfano G, Pittiglio M, Ferri C, Romaniello R, Oliviero G, Cancelli Y Int Urol Nephrol. 2024; .

PMID: 39738858 DOI: 10.1007/s11255-024-04309-w.


Analyzing Cell-free Genomic DNA in Spent Culture Media: Noninvasive Insight into the Blastocysts.

Layek S, Kanani S, Doultani S, Gohil T, Patil S, Sudhakar A Glob Med Genet. 2024; 11(3):227-232.

PMID: 39045037 PMC: 11265834. DOI: 10.1055/s-0044-1788260.

References
1.
Niba E, Tran V, Tuan-Pham L, Vu D, Nguyen N, Ta V . Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene. Clin Chim Acta. 2014; 436:155-9. DOI: 10.1016/j.cca.2014.05.018. View

2.
Chen Y, Gong Y, Dou L, Zhou X, Zhang Y . Bioinformatics analysis methods for cell-free DNA. Comput Biol Med. 2022; 143:105283. DOI: 10.1016/j.compbiomed.2022.105283. View

3.
Kurdyukov S, Bullock M . DNA Methylation Analysis: Choosing the Right Method. Biology (Basel). 2016; 5(1). PMC: 4810160. DOI: 10.3390/biology5010003. View

4.
Kohler C, Radpour R, Barekati Z, Asadollahi R, Bitzer J, Wight E . Levels of plasma circulating cell free nuclear and mitochondrial DNA as potential biomarkers for breast tumors. Mol Cancer. 2009; 8:105. PMC: 2780981. DOI: 10.1186/1476-4598-8-105. View

5.
Penyige A, Marton E, Soltesz B, Szilagyi-Bonizs M, Poka R, Lukacs J . Circulating miRNA Profiling in Plasma Samples of Ovarian Cancer Patients. Int J Mol Sci. 2019; 20(18). PMC: 6769773. DOI: 10.3390/ijms20184533. View