Division of Genetics and Metabolism, Department of Medical Research, Mackay Memorial Hospital, Taipei, Taiwan.
Orphanet J Rare Dis. 2013 Sep 22;8:147. doi: 10.1186/1750-1172-8-147.
Mucopolysaccharidosis type I (MPS I) is a genetic disease caused by the deficiency of α-L-iduronidase (IDUA) activity. MPS I is classified into three clinical phenotypes called Hurler, Scheie, and Hurler-Scheie syndromes according to their clinical severity. Treatments for MPS I are available. Better outcomes are associated with early treatment, which suggests a need for newborn screening for MPS I. The goal of this study was to determine whether measuring IDUA activity in dried blood on filter paper was effective in newborn screening for MPS I.
We conducted a newborn screening pilot program for MPS I from October 01, 2008 to April 30, 2013. Screening involved measuring IDUA activity in dried blood spots from 35,285 newborns using a fluorometric assay.
Of the 35,285 newborns screened, 19 did not pass the tests and had been noticed for a recall examination. After completing further recheck process, 3 were recalled again for leukocyte IDUA enzyme activity testing. Two of the three had deficient leukocyte IDUA activity. Molecular DNA analyses confirmed the diagnosis of MPS I in these two newborns.
It is feasible to use the IDUA enzyme assay for newborn screening. The incidence of MPS I in Taiwan estimated from this study is about 1/17,643.
黏多糖贮积症 I 型(MPS I)是一种由于α-L-艾杜糖苷酸酶(IDUA)活性缺乏引起的遗传疾病。根据其临床严重程度,MPS I 可分为三种临床表型,分别称为 Hurler、Scheie 和 Hurler-Scheie 综合征。目前已有针对 MPS I 的治疗方法。早期治疗与更好的疗效相关,这表明有必要对 MPS I 进行新生儿筛查。本研究旨在确定滤纸干血斑 IDUA 活性测定是否可有效用于 MPS I 的新生儿筛查。
我们于 2008 年 10 月 1 日至 2013 年 4 月 30 日开展了 MPS I 的新生儿筛查试点项目。筛查采用荧光分析法检测 35285 例新生儿滤纸干血斑 IDUA 活性。
在 35285 例接受筛查的新生儿中,有 19 例未通过检测,被注意到需要召回检查。进一步复查后,有 3 例因白细胞 IDUA 酶活性检测而再次召回。其中 2 例白细胞 IDUA 活性缺乏。分子 DNA 分析证实了这两名新生儿的 MPS I 诊断。
使用 IDUA 酶分析法进行新生儿筛查是可行的。本研究估计台湾地区 MPS I 的发病率约为 1/17643。