Quantitative RT PCR in the Diagnosis of Congenital Cytomegalovirus Infection with Special Reference to Sensorineural Hearing Loss in a Tertiary Care Centre in North Kerala
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Abstract
Background:Cytomegalovirus, a Herpes virus is the most common virus causing congenital viral infections. Sensorineueal hearing loss is the most common non hereditary manifestation. Majority of the babies are asymptomatic or have non specific symptoms at birth. An early diagnosis can help in starting antiviral treatment based on the clinical disease to prevent end organ damage and to intervene early in babies with hearing impairment which can reduce long term sequelae. Objectives :The aim of the study is to diagnose and quantitate neonatal CMV infection by qRTPCR (Quantitative Real Time Polymerase Chain Reaction) ,to evaluate the proportion and clinical profile of congenital CMV infections in a tertiary care hospital. Materials and Methods:This cross sectional diagnostic evaluation was done in the Dept. of Microbiology and Neonatal unit of Dept of Paediatrics, Govt Medical college .Kozhikode from August 2017 to December 2018. Details of demographic data, clinical profile, and CMV viral load in urine in various clinical infections were obtained and analyzed. Urine samples from 225 babies were received and processed in the Microbiology Department. DNA isolation and amplification was performed using commercial DNA extraction kit and CMV PCR kit for detection and quantification of CMV. Results:Of 225 babies with clinical features suggestive of CMV infection, CMV-DNA was detected and quantitated in urine of 27 babies (12%). The most common clinical presentation was hearing impairment, seen in 22 babies. Conclusion:RT-qPCR helps in diagnosing and quantitating CMV in congenital neonatal infection which helps in deciding on therapy and assessing response to treatment and can predict risk for long term sequelae. Diagnosis of congenital CMV in the newborn period is important for identifying those with neurologic abnormalities where appropriate treatment and management is essential.
背景:巨细胞病毒是一种疱疹病毒,是引起先天性病毒感染最常见的病毒。感觉神经性听力损失是最常见的非遗传性表现。大多数婴儿在出生时无症状或无特异性症状。早期诊断有助于根据临床疾病开始抗病毒治疗,以防止终末器官损伤,并对听力障碍婴儿进行早期干预,从而减少长期后遗症。目的:应用qRTPCR (Quantitative Real Time Polymerase Chain Reaction,实时定量聚合酶链反应)技术对新生儿巨细胞病毒感染进行诊断和定量,评价某三级医院先天性巨细胞病毒感染的比例和临床特征。材料与方法:本研究于2017年8月至2018年12月在科日科德公立医学院儿科微生物科和新生儿科进行横断面诊断评估。获得并分析了各种临床感染的人口学数据、临床概况和尿中巨细胞病毒载量的细节。微生物科接收并处理了225名婴儿的尿样。采用商用DNA提取试剂盒和CMV PCR试剂盒进行DNA分离扩增,检测和定量CMV。结果:在225例有CMV感染临床特征的婴儿中,27例(12%)在尿液中检测并定量CMV- dna。最常见的临床表现是听力障碍,22名婴儿出现过。结论:RT-qPCR有助于先天性新生儿感染巨细胞病毒的诊断和定量,有助于决定治疗方案和评估治疗反应,并可预测长期后遗症的风险。新生儿期先天性巨细胞病毒的诊断对于识别那些有神经系统异常的人是重要的,在那里适当的治疗和管理是必不可少的。