Frazier D M, Millington D S, McCandless S E, Koeberl D D, Weavil S D, Chaing S H, Muenzer J
Division of Genetics and Metabolism, Department of Pediatrics, University of North Carolina, Chapel Hill, 27599, USA.
J Inherit Metab Dis. 2006 Feb;29(1):76-85. doi: 10.1007/s10545-006-0228-9.
North Carolina (NC) was the first US state to initiate universal tandem mass spectrometry (MS/MS) newborn screening. This began as a statewide pilot project in 1997 to determine the incidence and feasibility of screening for fatty acid oxidation, organic acid and selected amino acid disorders. The MS/MS analyses were done by a commercial laboratory and all follow-up and confirmatory testing was performed through the NC Newborn Screening (NBS) Program. In April 1999, the NC NBS Laboratory began the MS/MS analyses in-house. Between 28 July 1997 and 28 July 2005, 944,078 infants were screened and 219 diagnoses were confirmed on newborns with elevated screening results, for an overall incidence of 1:4,300. Ninety-nine infants were identified with fatty acid oxidation disorders, 58 with organic acidaemias and 62 with aminoacidopathies. Medium-chain acyl-CoA dehydrogenase deficiency, 3-methylcrotonyl-CoA carboxylase deficiency and disorders of phenylalanine metabolism were the most common disorders detected. Identification of affected infants has allowed retrospective testing of other family members, resulting in an additional 16 diagnoses. Seven neonates died from complications of their metabolic disorders/prematurity despite timely MS/MS screening. In addition, there were six infants who were not identified by elevated NBS results but who presented with symptoms later in infancy. The NC MS/MS NBS Program uses a two-tier system, categorizing results as either 'borderline' or 'diagnostic' elevated, for both the cutoffs and follow-up protocol. Infants with an initial borderline result had only a repeat screen. Infants with a diagnostic or two borderline results were referred for confirmatory testing. The positive predictive value of the NC MS/MS NBS for those infants requiring confirmatory testing was 53% for 2003 and 2004. The success of the NC MS/MS NBS Program in identifying infants with metabolic disorders was dependent on a comprehensive follow-up protocol integrating the public health laboratory and the academic metabolic centres.
北卡罗来纳州(NC)是美国首个启动串联质谱(MS/MS)新生儿筛查的州。这始于1997年的一项全州范围的试点项目,以确定脂肪酸氧化、有机酸和特定氨基酸紊乱筛查的发病率和可行性。MS/MS分析由一家商业实验室进行,所有后续和确诊检测均通过北卡罗来纳州新生儿筛查(NBS)项目进行。1999年4月,北卡罗来纳州NBS实验室开始内部进行MS/MS分析。在1997年7月28日至2005年7月28日期间,对944,078名婴儿进行了筛查,对筛查结果升高的新生儿确诊了219例,总体发病率为1:4,300。确定了99名患有脂肪酸氧化紊乱的婴儿,58名患有有机酸血症的婴儿和62名患有氨基酸病的婴儿。中链酰基辅酶A脱氢酶缺乏症、3-甲基巴豆酰辅酶A羧化酶缺乏症和苯丙氨酸代谢紊乱是检测到的最常见疾病。对受影响婴儿的鉴定使得能够对其他家庭成员进行回顾性检测,又确诊了16例。尽管进行了及时的MS/MS筛查,仍有7名新生儿死于代谢紊乱/早产并发症。此外,有6名婴儿在新生儿筛查结果未升高时未被识别,但在婴儿期后期出现了症状。北卡罗来纳州MS/MS新生儿筛查项目使用两级系统,将结果分类为“临界”或“诊断性”升高,用于临界值和后续方案。初始结果为临界的婴儿仅进行重复筛查。诊断性或两个临界结果的婴儿被转诊进行确诊检测。2003年和2004年,北卡罗来纳州MS/MS新生儿筛查对那些需要确诊检测的婴儿的阳性预测值为53%。北卡罗来纳州MS/MS新生儿筛查项目在识别患有代谢紊乱的婴儿方面的成功取决于整合公共卫生实验室和学术代谢中心的全面后续方案。