The Limitations of Cytomegalovirus DNA Detection in Cerebrospinal Fluid of Newborn Infants With Congenital CMV Infection: A Tertiary Care Neonatal Center Experience.

Justyna Czech-Kowalska, Dominika Jedlińska-Pijanowska, Beata Kasztelewicz, Magdalena Kłodzińska, Aleksandra Pietrzyk, Eliza Sarkaria, Dorota Dunin-Wąsowicz, Kinga Gradowska, Anna Niezgoda, Dariusz Gruszfeld, Anna Dobrzańska
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引用次数: 5

Abstract

Background: Congenital cytomegalovirus (cCMV) infection of the central nervous system (CNS) can cause ventriculomegaly, gliosis, calcifications and cortical defects. Detection of CMV DNA in cerebrospinal fluid by PCR (CSF-CMV-PCR) is a marker of CNS involvement.

Objective: To evaluate a diagnostic value of the positive CSF-CMV-PCR in cCMV.

Methods: Analysis of clinical, laboratory, neuroimaging and single-nucleotide polymorphisms (SNPs) data according to the results of CSF-CMV-PCR were performed in infants with cCMV.

Results: A total of 168 infants were included; 145 (86.3%) had negative and 23 (13.7%) had positive CSF-CMV-PCR results. Associations between the positive CSF-CMV-PCR results and prematurity (odds ratio [OR] = 3.24; 95% confidence interval [CI]: 1.30-8.07), microcephaly (OR = 5.67; 95% CI: 2.08-15.41), seizures (OR = 4.15; 95% CI: 1.10-15.67), sensorineural hearing loss (OR = 6.6; 95% CI: 2.49-17.46), splenomegaly (OR = 8.13; 95% CI: 3.12-21.16), hepatitis (OR = 10.51; 95% CI: 3.31-33.35), petechiae (OR = 10.21; 95% CI: 3.78-27.57) and heterozygous T/C genotype at TLR4rs4986791 (OR = 7.88; 95% CI: 1.55-40.12) were observed. When using a multivariate logistic regression analysis, only the presence of severe sensorineural hearing loss (OR = 7.18; 95% CI: 1.75-29.34, P = 0.006), cystic lesions on MRI (OR 5.29; 95% CI: 1.31-21.36, P = 0.02), and calcifications on MRI (OR = 7.19; 95% CI: 1.67-30.97, P = 0.008) remained as the significant independent predictors of the positive CSF-CMV-PCR results.

Conclusions: The detection of CMV DNA in CSF is associated with a higher rate of CNS damage including abnormal MRI neuroimaging and severe hearing loss. Therefore, detection of CMV DNA in CSF may be considered as a marker of severe CNS injury in cCMV infection. However, the very low prevalence of the positive CSF-CMV-PCR results, even in infants with proven CNS involvement, may imply its limited role in clinical practice.

先天性巨细胞病毒感染新生儿脑脊液巨细胞病毒DNA检测的局限性:三级护理新生儿中心经验。
背景:先天性巨细胞病毒(cCMV)感染中枢神经系统(CNS)可引起脑室肿大、胶质瘤、钙化和皮质缺损。脑脊液CMV DNA的PCR检测(CSF-CMV-PCR)是中枢神经系统受累的标志。目的:探讨CSF-CMV-PCR阳性对cCMV的诊断价值。方法:根据CSF-CMV-PCR结果对cCMV患儿的临床、实验室、神经影像学及单核苷酸多态性(snp)数据进行分析。结果:共纳入168例婴儿;CSF-CMV-PCR阴性145例(86.3%),阳性23例(13.7%)。CSF-CMV-PCR阳性结果与早产的相关性(优势比[OR] = 3.24;95%可信区间[CI]: 1.30-8.07),小头畸形(OR = 5.67;95% CI: 2.08-15.41),癫痫发作(OR = 4.15;95% CI: 1.10-15.67),感音神经性听力损失(OR = 6.6;95% CI: 2.49-17.46),脾肿大(OR = 8.13;95% CI: 3.12-21.16),肝炎(OR = 10.51;95% CI: 3.31-33.35)、瘀点(OR = 10.21;95% CI: 3.78-27.57)和TLR4rs4986791的杂合T/C基因型(OR = 7.88;95% CI: 1.55 ~ 40.12)。当使用多变量logistic回归分析时,仅存在严重感音神经性听力损失(OR = 7.18;95% CI: 1.75-29.34, P = 0.006), MRI上的囊性病变(OR 5.29;95% CI: 1.31-21.36, P = 0.02), MRI显示钙化(OR = 7.19;95% CI: 1.67-30.97, P = 0.008)仍然是CSF-CMV-PCR阳性结果的重要独立预测因子。结论:脑脊液中CMV DNA的检测与CNS损伤的高发率相关,包括异常的MRI神经成像和严重的听力损失。因此,脑脊液中CMV DNA的检测可能被认为是cCMV感染时中枢神经系统严重损伤的标志。然而,CSF-CMV-PCR阳性结果的发生率非常低,即使在已证实有中枢神经系统受累的婴儿中也是如此,这可能意味着其在临床实践中的作用有限。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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