Messina MariaAnna, Meli Concetta, Raudino Federica, Pittalá Annarita, Arena Alessia, Barone Rita, Giuffrida Fortunata, Iacobacci Riccardo, Muccilli Vera, Sorge Giovanni, Fiumara Agata
Referral Center for Inherited Metabolic Diseases, Pediatric Clinical, AOU Policlinico-VE, Via Santa Sofia 78, 95123 Catania, Italy.
Child Neurology and Psichiatry, AOU Policlinico-VE, Via Santa Sofia 78, 95123 Catania, Italy.
Int J Neonatal Screen. 2018 Apr 5;4(2):12. doi: 10.3390/ijns4020012. eCollection 2018 Jun.
The expanded newborn screening for selected inborn errors of metabolism (IEM) in Sicily was introduced in 2007 by a Regional project entitled "Early detection of congenital metabolic diseases: expanded neonatal screening". It established two newborn screening laboratories, for Western and Eastern Sicily, which started their activity in 2011. Here we present the results of expanded screening (excluding phenylketonuria (PKU)) of the Eastern laboratory from January 2011 to December 2017. Our data highlight the importance of the expanded newborn screening as a basic health program to avoid the underestimation of rare diseases and the need of further investigations even when there are no textbook alterations of the metabolic profiles. We performed our analysis on dried blood spot by tandem mass spectrometry, according to Italian guidelines. A total of 196 samples from 60,408 newborns gave positive screening results (recall rate 0.32%) while 12 babies were true positive, including 2 newborns whose mothers resulted in being affected by a metabolic disease. The overall frequency of IEM found in the screening panel was 1:6041 (mothers excluded) or 1:5034 (mothers included). The introduction of MS/MS technology in Sicily has significantly increased the detection of inherited metabolic disorders, including those not previously covered, with a predictable improved outcome for several disorders.
西西里岛针对特定先天性代谢缺陷(IEM)开展的扩大新生儿筛查于2007年由一个名为“先天性代谢疾病的早期检测:扩大新生儿筛查”的区域项目引入。该项目设立了两个新生儿筛查实验室,分别位于西西里岛西部和东部,于2011年开始运作。在此,我们展示了东部实验室在2011年1月至2017年12月期间扩大筛查(不包括苯丙酮尿症(PKU))的结果。我们的数据突出了扩大新生儿筛查作为一项基础健康项目的重要性,即避免对罕见疾病的漏诊,以及即使代谢谱没有典型改变时仍需进一步检查的必要性。我们按照意大利指南,通过串联质谱法对干血斑进行分析。在60408名新生儿的196份样本中筛查结果呈阳性(召回率0.32%),其中12名婴儿为真正阳性,包括2名母亲患有代谢疾病的新生儿。在筛查组中发现的IEM总体发生率为1:6041(不包括母亲)或1:5034(包括母亲)。西西里岛引入串联质谱技术显著提高了对遗传性代谢疾病的检测率,包括那些以前未涵盖的疾病,预计会改善多种疾病的预后。