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宏基因组下一代测序在感染性脑炎和脑膜炎诊断中的应用:一项 213 例患者的大型前瞻性病例系列研究。

Metagenomic Next-Generation Sequencing for Diagnosis of Infectious Encephalitis and Meningitis: A Large, Prospective Case Series of 213 Patients.

机构信息

Department of Neurology, Hainan Hospital of PLA General Hospital, Sanya, China.

Department of Neurology, First Medical Center of PLA General Hospital, Beijing, China.

出版信息

Front Cell Infect Microbiol. 2020 Mar 5;10:88. doi: 10.3389/fcimb.2020.00088. eCollection 2020.

DOI:10.3389/fcimb.2020.00088
PMID:32211343
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7066979/
Abstract

We assessed the performance of metagenomic next-generation sequencing (mNGS) in the diagnosis of infectious encephalitis and meningitis. This was a prospective multicenter study. Cerebrospinal fluid samples from patients with viral encephalitis and/or meningitis, tuberculous meningitis, bacterial meningitis, fungal meningitis, and non-central nervous system (CNS) infections were subjected to mNGS. In total, 213 patients with infectious and non-infectious CNS diseases were finally enrolled from November 2016 to May 2019; the mNGS-positive detection rate of definite CNS infections was 57.0%. At a species-specific read number (SSRN) ≥2, mNGS performance in the diagnosis of definite viral encephalitis and/or meningitis was optimal (area under the curve [AUC] = 0.659, 95% confidence interval [CI] = 0.566-0.751); the positivity rate was 42.6%. At a genus-specific read number ≥1, mNGS performance in the diagnosis of tuberculous meningitis (definite or probable) was optimal (AUC=0.619, 95% CI=0.516-0.721); the positivity rate was 27.3%. At SSRNs ≥5 or 10, the diagnostic performance was optimal for definite bacterial meningitis (AUC=0.846, 95% CI = 0.711-0.981); the sensitivity was 73.3%. The sensitivities of mNGS (at SSRN ≥2) in the diagnosis of cryptococcal meningitis and cerebral aspergillosis were 76.92 and 80%, respectively. mNGS of cerebrospinal fluid effectively identifies pathogens causing infectious CNS diseases. mNGS should be used in conjunction with conventional microbiological testing. Chinese Clinical Trial Registry, ChiCTR1800020442.

摘要

我们评估了宏基因组下一代测序(mNGS)在诊断感染性脑炎和脑膜炎中的性能。这是一项前瞻性多中心研究。对病毒性脑炎和/或脑膜炎、结核性脑膜炎、细菌性脑膜炎、真菌性脑膜炎和非中枢神经系统(CNS)感染患者的脑脊液样本进行了 mNGS 检测。2016 年 11 月至 2019 年 5 月,共纳入 213 例感染性和非感染性中枢神经系统疾病患者;明确中枢神经系统感染的 mNGS 阳性检出率为 57.0%。在物种特异性读长数(SSRN)≥2 时,mNGS 对明确病毒性脑炎和/或脑膜炎的诊断性能最佳(曲线下面积[AUC] = 0.659,95%置信区间[CI] = 0.566-0.751);阳性率为 42.6%。在属特异性读长数≥1 时,mNGS 对结核性脑膜炎(明确或可能)的诊断性能最佳(AUC=0.619,95%CI=0.516-0.721);阳性率为 27.3%。在 SSRN≥5 或 10 时,mNGS 对明确细菌性脑膜炎的诊断性能最佳(AUC=0.846,95%CI=0.711-0.981);敏感性为 73.3%。mNGS(在 SSRN≥2 时)对隐球菌性脑膜炎和脑曲霉病的诊断敏感性分别为 76.92%和 80%。mNGS 可有效鉴定引起感染性中枢神经系统疾病的病原体。mNGS 应与常规微生物检测相结合使用。中国临床试验注册中心,ChiCTR1800020442。

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