Meyer Lucy, Sharon Bazak, Huang Tina C, Meyer Abby C, Gravel Kristin E, Schimmenti Lisa A, Swanson Elizabeth C, Herd Hannah E, Hernandez-Alvarado Nelmary, Coverstone Kirsten R, McCann Mark, Schleiss Mark R
Center for Infectious Diseases and Microbiology Translational Research, Department of Pediatrics, Division of Pediatric Infectious Diseases and Immunology, University of Minnesota Medical School, Minneapolis, MN, United States.
Lions Children's Hearing Center, University of Minnesota Medical Center/Fairview Health Services, Minneapolis, MN, United States.
Am J Otolaryngol. 2017 Sep-Oct;38(5):565-570. doi: 10.1016/j.amjoto.2017.06.002. Epub 2017 Jun 7.
Congenital cytomegalovirus (cCMV) infection is the most common non-genetic cause of sensorineural hearing loss (SNHL). However, accurate diagnosis of cCMV as the etiology of SNHL is problematic beyond the neonatal period. This study therefore examined whether cCMV infection could be identified retrospectively in children presenting with unexplained SNHL to a multidisciplinary diagnostic outpatient otolaryngology clinic at an academic medical center in Minnesota.
Over a 4-year period, 57 patients with an age range of 3months to 10years with unexplained SNHL were recruited to participate in this study. Informed consent was obtained to test the archived dried blood spots (DBS) of these patients for cCMV infection by real-time PCR, targeting a highly conserved region of the CMV UL83 gene. Results were normalized to recovery of an NRAS gene control. Chart review was conducted to identify subjects who underwent genetic testing and/or neurodiagnostic imaging to investigate possible genetic, syndromic, or anatomical causes of SNHL.
In total, 15 of the 57 children with unexplained SNHL tested positive for CMV DNA in their DBS (26%). A mean viral load of 8.3×10 (±4.1×10) [range, 1×10-6×10] copies/μg DNA was observed in subjects retrospectively diagnosed with cCMV. No statistically significant correlation was found between viral load and SNHL severity.
A retrospective DBS analysis demonstrated that 26% of patients presenting with unexplained SNHL in childhood had cCMV. DBS testing is useful in the retrospective diagnosis of cCMV, and may provide definitive diagnostic information about the etiology of SNHL.
先天性巨细胞病毒(cCMV)感染是感音神经性听力损失(SNHL)最常见的非遗传病因。然而,在新生儿期之后,准确诊断cCMV作为SNHL的病因存在问题。因此,本研究调查了在明尼苏达州一家学术医疗中心的多学科诊断门诊耳鼻喉科诊所就诊的不明原因SNHL儿童中,是否可以回顾性地识别出cCMV感染。
在4年期间,招募了57例年龄在3个月至10岁之间、不明原因SNHL的患者参与本研究。获得知情同意后,通过实时PCR检测这些患者的存档干血斑(DBS)中是否存在cCMV感染,以CMV UL83基因的高度保守区域为靶点。结果以NRAS基因对照的回收率进行标准化。进行病历审查以识别接受基因检测和/或神经诊断成像以调查SNHL可能的遗传、综合征或解剖学病因的受试者。
在57例不明原因SNHL的儿童中,共有15例(26%)的DBS检测出CMV DNA呈阳性。在回顾性诊断为cCMV的受试者中,观察到平均病毒载量为8.3×10(±4.1×10)[范围,1×10 - 6×10]拷贝/μg DNA。未发现病毒载量与SNHL严重程度之间存在统计学显著相关性。
回顾性DBS分析表明,26%的童年期不明原因SNHL患者患有cCMV。DBS检测在cCMV的回顾性诊断中有用,并且可能为SNHL的病因提供明确的诊断信息。