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Parasite Circulating Cell-free DNA in the Blood of Alveolar Echinococcosis Patients As a Diagnostic and Treatment-Status Indicator

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Journal Clin Infect Dis
Date 2020 Nov 4
PMID 33146713
Citations 3
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Abstract

Background: Alveolar echinococcosis (AE) is a serious parasitic disease caused by the larvae of Echinococcus multilocularis. It is the less common but substantially more deadly of the 2 major echinococcosis diseases that can occur globally but are concentrated in central Asia.

Methods: We analyzed parasite circulating cell-free DNA (cfDNA) in 149 plasma samples using a DNA sequencing-based method (105 AE, 16 cystic echinococcosis, 4 liver cancer, 4 gallstones, and 20 healthy volunteers). After identifying the Echinococcus-specific cfDNA (Em-cfDNA) sequences in the samples, we determined whether Em-cfDNA could be used for AE diagnosis and as a potential indicator of the effectiveness of surgical treatment. We also examined potential associations between Em-cfDNA levels and clinical features of AE patients.

Results: Our work demonstrates that varying reads of Em-cfDNA were detectable in the plasma of 100% of preoperative AE patients and that all of the non-AE patients and healthy volunteers were negative. Em-cfDNA has good sensitivity and specificity for the diagnosis of AE. We also found that Em-cfDNA levels apparently have reference value for evaluating the therapeutic efficacy of surgery interventions for AE lesions. Finally, our analysis revealed that Em-cfDNA levels can reflect meaningful information about lesion size in preoperative AE patients.

Conclusions: We demonstrate that sequencing-based monitoring of Em-cfDNA can be used in the clinic as a powerful diagnostic indicator for AE. We also note that there is a strong potential for use of this liquid-biopsy method to monitor ongoing disease status in postintervention AE patients.

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Advances in Novel Diagnostic Techniques for Alveolar Echinococcosis.

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Luo X, Jiang P, Ma J, Li Z, Zhou J, Wei X Front Microbiol. 2024; 15:1413532.

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Knapp J, Lallemand S, Monnien F, Felix S, Valmary-Degano S, Courquet S Parasite. 2022; 29:4.

PMID: 35113014 PMC: 8812296. DOI: 10.1051/parasite/2022004.