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新生儿黏多糖贮积症II型筛查:经验教训

Newborn screening for mucopolysaccharidosis type II: Lessons learned.

作者信息

Burton Barbara K, Shively Vera, Quadri Allegra, Warn Lauren, Burton Jennifer, Grange Dorothy K, Christensen Katherine, Groepper Daniel, Ashbaugh Laura, Ehrhardt Joan, Basheeruddin Khaja

机构信息

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA; Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.

出版信息

Mol Genet Metab. 2023 Sep-Oct;140(1-2):107557. doi: 10.1016/j.ymgme.2023.107557. Epub 2023 Mar 6.

Abstract

We describe our experience with population-based newborn screening for mucopolysaccharidosis type II (MPS II) in 586,323 infants by measurement of iduronate-2-sulfatase activity in dried blood spots between December 12, 2017 and April 30, 2022. A total of 76 infants were referred for diagnostic testing, 0.01% of the screened population. Of these, eight cases of MPS II were diagnosed for an incidence of 1 in 73,290. At least four of the eight cases detected had an attenuated phenotype. In addition, cascade testing revealed a diagnosis in four extended family members. Fifty-three cases of pseudodeficiency were also identified, for an incidence of 1 in 11,062. Our data suggest that MPS II may be more common than previously recognized with a higher prevalence of attenuated cases.

摘要

我们描述了2017年12月12日至2022年4月30日期间,通过检测干血斑中的艾杜糖醛酸-2-硫酸酯酶活性,对586,323名婴儿进行基于人群的II型黏多糖贮积症(MPS II)新生儿筛查的经验。共有76名婴儿被转诊进行诊断测试,占筛查人群的0.01%。其中,确诊8例MPS II,发病率为1/73,290。在检测出的8例病例中,至少有4例为症状较轻的表型。此外,级联检测在4名大家庭成员中确诊。还发现了53例假性缺陷病例,发病率为1/11,062。我们的数据表明,MPS II可能比以前认为的更常见,症状较轻病例的患病率更高。

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