Luo Xiaoqin, Jiang Ping, Ma Jideng, Li Zian, Zhou Jianwu, Wei Xiaoxing, A Jide, Chai Jinping, Lv Yanke, Cheng Peng, Cao Chunhua, A Xiangren
Qinghai University, Xining, China.
Department of Clinical Laboratory, Qinghai Provincial People's Hospital, Xining, China.
Front Microbiol. 2024 Jul 3;15:1413532. doi: 10.3389/fmicb.2024.1413532. eCollection 2024.
Echinococcosis is a chronic zoonotic disease caused by tapeworms of the genus . The World Health Organization (WHO) has identified encapsulated disease as one of 17 neglected diseases to be controlled or eliminated by 2050. There is no accurate, early, non-invasive molecular diagnostic method to detect echinococcosis. The feasibility of circulating free DNA as a diagnostic method for echinococcosis has yielded inconclusive results in a number of published studies. However, there has been no systematic evaluation to date assessing the overall performance of these assays. We report here the first meta-analysis assessing the diagnostic accuracy of cfDNA in plasma, serum, and urine for echinococcosis.
We systematically searched PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure (CNKI), and WeiPu databases up to 17 January 2024, for relevant studies. All analyses were performed using RevMan 5.3, Meta-DiSc 1.4, Stata 17.0, and R 4.3.1 software. The sensitivity, specificity, and other accuracy indicators of circulating free DNA for the diagnosis of echinococcosis were summarized. Subgroup analyses and meta-regression were performed to identify sources of heterogeneity.
A total of 7 studies included 218 patients with echinococcosis and 214 controls (156 healthy controls, 32 other disease controls (non-hydatid patients), and 26 non-study-targeted echinococcosis controls were included). Summary estimates of the diagnostic accuracy of cfDNA in the diagnosis of echinococcosis were as follows: sensitivity (SEN) of 0.51 (95% CI: 0.45-0.56); specificity (SPE) of 0.99 (95% CI: 0.97-0.99); positive likelihood ratio (PLR) of 11.82 (95% CI: 6.74-20.74); negative likelihood ratio (NLR) of 0.57 (95% CI: 0.41-0.80); diagnostic ratio (DOR) of 36.63 (95% CI: 13.75-97.59); and area under the curve (AUC) value of 0.98 (95% CI: 0.96-1.00).
Existing evidence indicates that the combined specificity of circulating cfDNA for echinococcosis is high. However, the combined sensitivity performance is unsatisfactory due to significant inter-study heterogeneity. To strengthen the validity and accuracy of our findings, further large-scale prospective studies are required.Systematic review registrationThe systematic review was registered in the International Prospective Register of Systematic Reviews PROSPERO [CRD42023454158]. https://www.crd.york.ac.uk/PROSPERO/.
棘球蚴病是一种由棘球属绦虫引起的慢性人畜共患病。世界卫生组织(WHO)已将包囊型疾病确定为到2050年要控制或消除的17种被忽视疾病之一。目前尚无准确、早期、非侵入性的分子诊断方法来检测棘球蚴病。循环游离DNA作为棘球蚴病诊断方法的可行性在一些已发表的研究中结果尚无定论。然而,迄今为止尚未有系统评价来评估这些检测方法的整体性能。我们在此报告第一项荟萃分析,评估血浆、血清和尿液中循环游离DNA(cfDNA)对棘球蚴病的诊断准确性。
我们系统检索了截至2024年1月17日的PubMed、Embase、Cochrane图书馆、中国知网(CNKI)和维普数据库,以查找相关研究。所有分析均使用RevMan 5.3、Meta-DiSc 1.4、Stata 17.0和R 4.3.1软件进行。总结了循环游离DNA诊断棘球蚴病的敏感性、特异性和其他准确性指标。进行亚组分析和Meta回归以确定异质性来源。
共有7项研究纳入了218例棘球蚴病患者和214例对照(包括156例健康对照、32例其他疾病对照(非包虫病患者)和26例非研究目标的棘球蚴病对照)。cfDNA诊断棘球蚴病的诊断准确性总结估计如下:敏感性(SEN)为0.51(95%CI:0.45 - 0.56);特异性(SPE)为0.99(95%CI:0.97 - 0.99);阳性似然比(PLR)为11.82(95%CI:6.74 - 20.74);阴性似然比(NLR)为0.57(95%CI:0.41 - 0.80);诊断比值比(DOR)为36.63(95%CI:13.75 - 97.59);曲线下面积(AUC)值为0.98(95%CI:0.96 - 1.00)。
现有证据表明,循环cfDNA对棘球蚴病的综合特异性较高。然而,由于研究间存在显著异质性,综合敏感性表现不尽人意。为加强我们研究结果的有效性和准确性,需要进一步开展大规模前瞻性研究。
系统评价注册
该系统评价已在国际前瞻性系统评价注册库PROSPERO[CRD42023454158]中注册。https://www.crd.york.ac.uk/PROSPERO/ 。