Song Junhyup, Kim Sinyoung, Kwak Eunmin, Park Younhee
Department of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Front Microbiol. 2023 Sep 19;14:1257124. doi: 10.3389/fmicb.2023.1257124. eCollection 2023.
Human cytomegalovirus (CMV) transmitted through breast milk poses fatal risks to preterm infants. However, current molecular assay systems often do not accommodate breast milk samples. In this study, we evaluated the analytical and clinical performance of the measurement procedure of CMV load in breast milk utilizing the Cobas CMV test on the Cobas 6,800 system. This was enabled by incorporating a simple independent sample preparation procedure before the application of samples on the automated assay system. Clinical data from electronic medical records were retrospectively analyzed. Breast milk samples from mothers of preterm infants born before 33 weeks of gestation were screened for CMV using the automated assay system. CMV positivity rates in breast milk and neonatal samples and the CMV transmission rate were calculated. Furthermore, to validate the analytical accuracy of the overall measurement procedure with newly obtained residual breast milk samples, the linearity of the measurement procedure was assessed, and a simplified sample preparation method was validated against a conventional method. The CMV positivity rates in maternal breast milk and neonatal samples were 57.8 and 5.2%, respectively. The CMV transmission rate through breast milk was 7.7%. No significant differences in gestational age or birth weight were found between the CMV-negative and CMV-positive neonates. The linearity of the procedure was observed within a range of 1.87-4.73 log IU/mL. The simplified sample preparation method had an equivalent or even improved CMV detection sensitivity than the conventional method. Incorporating a simple independent sample preparation procedure effectively resolved any potential issues regarding the application of breast milk on the automated assay system. Our approach contributed to reduced vertical transmission of CMV by providing a convenient and reliable method for the monitoring of breast milk CMV positivity for clinicians.
通过母乳传播的人巨细胞病毒(CMV)对早产儿构成致命风险。然而,目前的分子检测系统往往无法处理母乳样本。在本研究中,我们利用Cobas 6800系统上的Cobas CMV检测法评估了母乳中CMV载量测量程序的分析性能和临床性能。这是通过在将样本应用于自动化检测系统之前纳入一个简单的独立样本制备程序来实现的。对电子病历中的临床数据进行了回顾性分析。使用自动化检测系统对妊娠33周前出生的早产儿母亲的母乳样本进行CMV筛查。计算了母乳和新生儿样本中的CMV阳性率以及CMV传播率。此外,为了用新获得的剩余母乳样本验证整个测量程序的分析准确性,评估了测量程序的线性,并针对传统方法验证了一种简化的样本制备方法。母亲母乳和新生儿样本中的CMV阳性率分别为57.8%和5.2%。通过母乳的CMV传播率为7.7%。CMV阴性和阳性新生儿在胎龄或出生体重方面未发现显著差异。在1.87 - 4.73 log IU/mL范围内观察到该程序的线性。简化的样本制备方法具有与传统方法相当甚至更高的CMV检测灵敏度。纳入一个简单的独立样本制备程序有效地解决了关于将母乳应用于自动化检测系统的任何潜在问题。我们的方法为临床医生提供了一种方便可靠的监测母乳CMV阳性的方法,有助于减少CMV的垂直传播。