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通过检测循环无细胞 DNA 和 miRNA 诊断包虫病。

Diagnosis of echinococcosis by detecting circulating cell-free DNA and miRNA.

机构信息

Department of parasitology and mycology, Faculty of medicine, Isfahan University of Medical sciences, Isfahan, Iran.

Research center for Hydatid disease in Iran, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Expert Rev Mol Diagn. 2023 Feb;23(2):133-142. doi: 10.1080/14737159.2023.2178903. Epub 2023 Feb 18.

Abstract

INTRODUCTION

Diagnosis of echinococcosis is difficult and usually performed based on clinical findings, imaging, and serological test. However, all of them have limitations, especially in follow-up approaches.

AREAS COVERED

Detection of cell-free DNA (cfDNA) and micro-RNA (miRNA) is currently a hot topic for diagnosis of echinococcosis diseases. For detecting cell-free DNA in echinococcosis patient's samples such as sera, some techniques are based on next-generation sequencing (NGS), DNA-deep sequencing, some are based on PCR-based methods, and a few works related to the detection of miRNA for the diagnosis of human echinococcosis.

EXPERT OPINION

In the detection of cell-free DNA in echinococcosis patient' samples, NGS and DNA-deep sequencing have shown high level of sensitivity, but are not suitable for routine clinical examination as they are expensive and inaccessible in the majority of endemic areas. However, PCR-based methods have shown a sensitivity of about 20-25%. To improve the sensitivity of these tests, improving the DNA extraction method, designing appropriate primers for detecting short-length fragments of circulating DNA, using a higher volume of a serum sample, and application of more sensitive PCR methods are recommended. In the field of miRNA detection, further works are recommended.

摘要

简介

包虫病的诊断较为困难,通常基于临床发现、影像学和血清学检查来进行。然而,所有这些方法都存在局限性,尤其是在随访方法中。

涵盖领域

游离细胞 DNA(cfDNA)和微 RNA(miRNA)的检测目前是包虫病诊断的热门话题。为了检测包虫病患者血清等样本中的游离 DNA,一些技术基于下一代测序(NGS)、深度 DNA 测序,一些基于基于 PCR 的方法,还有一些与 miRNA 检测相关的工作用于诊断人类包虫病。

专家意见

在包虫病患者样本中游离 DNA 的检测方面,NGS 和深度 DNA 测序显示出较高的灵敏度,但由于价格昂贵且在大多数流行地区无法获得,因此不适合常规临床检查。然而,基于 PCR 的方法显示出约 20-25%的灵敏度。为了提高这些检测的灵敏度,建议改进 DNA 提取方法、设计用于检测循环 DNA 短片段的适当引物、使用更大体积的血清样本,并应用更敏感的 PCR 方法。在 miRNA 检测领域,建议开展更多的相关工作。

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