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本文引用的文献

1
Impact of age at onset and newborn screening on outcome in organic acidurias.发病年龄和新生儿筛查对有机酸尿症预后的影响。
J Inherit Metab Dis. 2016 May;39(3):341-353. doi: 10.1007/s10545-015-9907-8. Epub 2015 Dec 21.
2
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype.有机酸尿症和尿素循环障碍的表型谱。第2部分:不断演变的临床表型。
J Inherit Metab Dis. 2015 Nov;38(6):1059-74. doi: 10.1007/s10545-015-9840-x. Epub 2015 Apr 15.
3
The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.有机酸血症和尿素循环障碍的表型谱。第1部分:初始表现。
J Inherit Metab Dis. 2015 Nov;38(6):1041-57. doi: 10.1007/s10545-015-9839-3. Epub 2015 Apr 15.
4
Newborn screening by tandem mass spectrometry for glutaric aciduria type 1: a cost-effectiveness analysis.串联质谱法在 1 型戊二酸血症新生儿筛查中的成本效益分析。
Orphanet J Rare Dis. 2013 Oct 17;8:167. doi: 10.1186/1750-1172-8-167.
5
A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document.启动欧盟新生儿筛查政策辩论的框架:一份专家意见文件。
Eur J Hum Genet. 2014 Jan;22(1):12-7. doi: 10.1038/ejhg.2013.90. Epub 2013 May 8.
6
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 1. From blood spot to screening result.欧洲的新生儿筛查计划;关于协调的争论和努力。第 1 部分。从血斑到筛查结果。
J Inherit Metab Dis. 2012 Jul;35(4):603-11. doi: 10.1007/s10545-012-9483-0. Epub 2012 May 3.
7
Newborn screening programmes in Europe; arguments and efforts regarding harmonization. Part 2. From screening laboratory results to treatment, follow-up and quality assurance.欧洲新生儿筛查计划;关于协调的争论和努力。第 2 部分。从筛查实验室结果到治疗、随访和质量保证。
J Inherit Metab Dis. 2012 Jul;35(4):613-25. doi: 10.1007/s10545-012-9484-z. Epub 2012 Apr 28.
8
Clinical and neurocognitive outcome in symptomatic isovaleric acidemia.症状性异戊酸血症的临床和神经认知结局。
Orphanet J Rare Dis. 2012 Jan 25;7:9. doi: 10.1186/1750-1172-7-9.
9
Propionic acidemia: neonatal versus selective metabolic screening.丙酸血症:新生儿期与选择性代谢筛查。
J Inherit Metab Dis. 2012 Jan;35(1):41-9. doi: 10.1007/s10545-011-9419-0. Epub 2011 Dec 2.
10
Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme.对扩展筛查项目中发现的先天性代谢缺陷婴儿进行评估和长期随访。
Mol Genet Metab. 2011 Dec;104(4):470-5. doi: 10.1016/j.ymgme.2011.09.021. Epub 2011 Sep 22.

欧洲的新生儿筛查项目:关于协调统一的争论与努力——以有机酸尿症为重点

Newborn Screening Programmes in Europe, Arguments and Efforts Regarding Harmonisation: Focus on Organic Acidurias.

作者信息

Hörster Friederike, Kölker Stefan, Loeber J Gerard, Cornel Martina C, Hoffmann Georg F, Burgard Peter

机构信息

Division of Neuropediatrics and Inherited Metabolic Diseases, Department of General Pediatrics, University Children's Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.

International Society for Neonatal Screening, Bilthoven, The Netherlands.

出版信息

JIMD Rep. 2017;32:105-115. doi: 10.1007/8904_2016_537. Epub 2016 Jun 26.

DOI:10.1007/8904_2016_537
PMID:27344647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5362556/
Abstract

BACKGROUND

The state of newborn screening (NBS) programmes for organic acidurias in Europe was assessed by a web-based questionnaire in the EU programme of Community Action in Public Health 2010/2011 among the - at that time - 27 EU member states, candidate countries, potential candidates and three EFTA countries.

RESULTS

Thirty-seven data sets from 39 target countries were analysed. Newborn screening for glutaric aciduria type I (GA-I) was performed in ten, for isovaleric aciduria (IVA) in nine and for methylmalonic aciduria including cblA, cblB, cblC and cblD (MMACBL) as well as for propionic aciduria (PA) in seven countries. Samples were obtained at a median age of 2.5 days and laboratory analysis began at median age of 4.5 days. Positive screening results were mostly confirmed in specialised centres by analysis of organic acids in urine. Confirmation of a positive screening result usually did not start before the second week of life (median ages: 9.5 days [IVA], 9 days [GA-I], 8.5 days [PA, MMACBL]) and was completed early in the third week of life (median ages: 15 days [IVA, PA, MMA], 14.5 days [GA-I]). Treatment was initiated in GA-I and IVA at a median age of 14 days and in MMACBL and PA at a median age of 15 days.

CONCLUSION

NBS for organic acidurias in Europe is variable and less often established than for amino acid disorders. While for GA-I its benefit has already been demonstrated, there is room for debate of NBS for IVA and especially PA and MMACBL.

摘要

背景

在2010/2011年欧盟公共卫生社区行动计划中,通过基于网络的调查问卷,对当时的27个欧盟成员国、候选国家、潜在候选国家以及三个欧洲自由贸易联盟国家中有机酸尿症新生儿筛查(NBS)项目的状况进行了评估。

结果

分析了来自39个目标国家的37个数据集。十个国家开展了I型戊二酸血症(GA-I)新生儿筛查,九个国家开展了异戊酸血症(IVA)筛查,七个国家开展了包括cblA、cblB、cblC和cblD型甲基丙二酸血症(MMACBL)以及丙酸血症(PA)的新生儿筛查。样本采集的中位年龄为2.5天,实验室分析开始的中位年龄为4.5天。筛查阳性结果大多在专门中心通过尿液有机酸分析得到确认。筛查阳性结果的确认通常在出生后第二周之前不会开始(中位年龄:IVA为9.5天,GA-I为9天,PA和MMACBL为8.5天),并在出生后第三周初完成(中位年龄:IVA、PA、MMA为15天,GA-I为14.5天)。GA-I和IVA治疗开始的中位年龄为14天,MMACBL和PA治疗开始的中位年龄为15天。

结论

欧洲有机酸尿症的新生儿筛查情况各不相同,且与氨基酸疾病相比,开展得较少。虽然GA-I的筛查益处已得到证实,但IVA尤其是PA和MMACBL的新生儿筛查仍存在争议空间。