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新生儿莫尔奎氏症和其他溶酶体贮积症的筛查:对 70000 名新生儿的 8 重分析检测结果。

Newborn screening for Morquio disease and other lysosomal storage diseases: results from the 8-plex assay for 70,000 newborns.

机构信息

Department of Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan.

Department of Pediatrics, National Taiwan University Hospital, and National Taiwan University College of Medicine, Taipei, Taiwan.

出版信息

Orphanet J Rare Dis. 2020 Feb 3;15(1):38. doi: 10.1186/s13023-020-1322-z.

Abstract

BACKGROUND

The necessity of early treatment for lysosomal storage diseases (LSDs) has triggered the development of newborn screening for LSDs in recent years. Here we report the first 70,000 newborns screened for Mucopolysaccharidosis (MPS) type 4A (Morquio syndrome) and other LSDs by an 8-plex assay including the original 4-plex LSD screening tandem mass spectrometry (MS/MS) assay for Pompe disease, Fabry disease, Gaucher disease, and MPS I disease.

METHODS

The additional reaction for MPS II, MPS 3B, MPS 4A, and MPS 6 enzymes was performed separately from the 4-plex reaction. The two reactions were quenched and extracted, then combined before carrying out a single 2-min UPLC-MS/MS analysis.

RESULTS

From Mar. 2018 to Apr. 2019, 73,743 newborns were screened with the 8-plex LSD screening assay. The 8-plex assay revealed a better analytical precision than the previous 4-plex assay possibly because the 8-plex was carried out using UPLC-MS/MS. Six newborns were found to have low MPS-4A enzyme (N-acetylgalactosamine-6-sulfatase) activity and biallelic GALNS pathogenic mutations in trans; these patients are presumably affected with MPS4A, making an incidence of one in 12,291 (95% confident interval (CI): 5633-26,817). One mutation, c.857C > T (p.T286 M) of the GALNS gene, accounted 5 of the 12 mutated alleles. These newborns had immature vertebral bodies at 1 month of age, and one case was treated with elosulfase alfa 2 mg/kg/week starting from 4 months of age. Among other MPSs screened, one case of MPS I, 3 cases of MPS II, and 3 cases of MPS 3B were detected. One case of mucolipidosis type III was also diagnosed. In conjunction with another 9 patients of Pompe disease, Gaucher disease, and classical Fabry disease, making an incidence of LSDs as one in 3206 newborns (95% CI: 2137 - 4811). The one with infantile-onset Pompe disease and the one with Gaucher disease were treated since the age of 8 days and 41 days respectively.

CONCLUSIONS

Routine newborn screening of MPS 4A and other LSDs were made possible by the 8-plex LSD screening assay. However, detailed phenotype prediction and the time to start treatment will need further elucidation.

摘要

背景

溶酶体贮积症(LSDs)早期治疗的必要性促使近年来开展 LSDs 的新生儿筛查。在此,我们报告首例通过 8 重分析物检测(包括用于庞贝病、法布雷病、戈谢病和黏多糖贮积症 I 型的原始 4 重 LSD 串联质谱(MS/MS)检测的新增庞贝病检测)筛查 70,000 名新生儿的 Mucopolysaccharidosis(MPS)4A(Morquio 综合征)和其他 LSDs。

方法

MPS II、MPS 3B、MPS 4A 和 MPS 6 酶的额外反应与 4 重反应分开进行。两个反应被淬灭并提取,然后在进行单一 2 分钟 UPLC-MS/MS 分析之前进行合并。

结果

2018 年 3 月至 2019 年 4 月,对 73743 名新生儿进行了 8 重 LSD 筛查检测。8 重分析物检测可能由于使用 UPLC-MS/MS 进行,其分析精度优于之前的 4 重检测。有 6 名新生儿被发现具有低 MPS-4A 酶(N-乙酰半乳糖胺-6-硫酸酯酶)活性和半合子 GALNS 致病性突变;这些患者可能患有 MPS4A,发病率为 12291 分之一(95%置信区间(CI):5633-26817)。GALNS 基因的 c.857C > T(p.T286 M)突变占 12 个突变等位基因的 5 个。这些新生儿在 1 月龄时出现不成熟的椎体,其中 1 例从 4 月龄开始接受每周 2mg/kg/周的艾拉司琼治疗。在筛查的其他黏多糖贮积症中,发现 1 例黏多糖贮积症 I 型、3 例黏多糖贮积症 II 型和 3 例黏多糖贮积症 3B 型。还诊断出 1 例黏脂贮积症 III 型。结合另外 9 例庞贝病、戈谢病和经典法布雷病患者,LSDs 的发病率为每 3206 名新生儿中有 1 例(95%CI:2137-4811)。1 例婴儿期起病的庞贝病患者和 1 例戈谢病患者分别在 8 天和 41 天开始治疗。

结论

通过 8 重 LSD 筛查检测,实现了 MPS 4A 和其他 LSDs 的常规新生儿筛查。然而,详细的表型预测和开始治疗的时间仍需进一步阐明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ca/6998831/c8af32066f6d/13023_2020_1322_Fig1_HTML.jpg

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