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Ⅰ型黏多糖贮积症新生儿筛查五年经验报告及文献综述

Report of Five Years of Experience in Neonatal Screening for Mucopolysaccharidosis Type I and Review of the Literature.

作者信息

Gragnaniello Vincenza, Gueraldi Daniela, Rubert Laura, Manzoni Francesca, Cazzorla Chiara, Giuliani Antonella, Polo Giulia, Salviati Leonardo, Burlina Alberto

机构信息

Division of Inherited Metabolic Diseases, Department of Diagnostic Services, University Hospital of Padua, via Orus 2/B, 35129 Padua, Italy.

Clinical Genetics Unit, Department of Diagnostic Services, University Hospital of Padua, via Giustiniani 2, 35129 Padua, Italy.

出版信息

Int J Neonatal Screen. 2020 Nov 2;6(4):85. doi: 10.3390/ijns6040085.

Abstract

Mucopolysaccharidosis type I (MPS I) is a progressive lysosomal storage disease, with neurological and visceral involvement, in which early diagnosis through newborn screening (NBS) and early treatment can improve outcomes. We present our first 5 years of experience with laboratory and clinical management of NBS for MPS I. Since 2015, we have screened 160,011 newborns by measuring α-L-iduronidase (IDUA) activity and, since 2019, glycosaminoglycans (GAGs) in dried blood spot (DBS) as a second-tier test. Positive screening patients were referred to our clinic for confirmatory clinical and molecular testing. We found two patients affected by MPS I (incidence of 1:80,005). Before the introduction of second-tier testing, we found a high rate of false-positives due to pseudodeficiency. With GAG analysis in DBS as a second-tier test, no false-positive newborns were referred to our clinic. The confirmed patients were early treated with enzyme replacement therapy and bone-marrow transplantation. For both, the clinical outcome of the disease is in the normal range. Our experience confirms that NBS for MPS I is feasible and effective, along with the need to include GAG assay as a second-tier test. Follow-up of the two positive cases identified confirms the importance of early diagnosis through NBS and early treatment to improve the outcome of these patients.

摘要

I型黏多糖贮积症(MPS I)是一种进行性溶酶体贮积病,累及神经和内脏,通过新生儿筛查(NBS)进行早期诊断并尽早治疗可改善预后。我们介绍了我们在MPS I新生儿筛查的实验室和临床管理方面的首个5年经验。自2015年以来,我们通过检测α-L-艾杜糖醛酸酶(IDUA)活性对160,011名新生儿进行了筛查,自2019年起,将干血斑(DBS)中的糖胺聚糖(GAGs)作为二线检测项目。筛查阳性的患者被转诊至我们的诊所进行确诊的临床和分子检测。我们发现了两名受MPS I影响的患者(发病率为1:80,005)。在引入二线检测之前,我们发现由于假缺陷导致的假阳性率很高。将DBS中的GAG分析作为二线检测后,没有假阳性新生儿被转诊至我们的诊所。确诊的患者接受了酶替代疗法和骨髓移植的早期治疗。对于这两名患者,疾病的临床结局均在正常范围内。我们的经验证实,MPS I的新生儿筛查是可行且有效的,同时需要将GAG检测作为二线检测项目。对确诊的两例阳性病例的随访证实了通过新生儿筛查进行早期诊断和尽早治疗以改善这些患者预后的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/968a/7712507/43b1a0a3fabc/IJNS-06-00085-g001.jpg

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