用滤纸上的干血点筛选糖原贮积病Ia型:COP-PCR在检测c.648G>T G6PC基因突变中的应用。

Q3 Medicine Kobe Journal of Medical Sciences Pub Date : 2021-11-02
Yogik Onky Silvana Wijaya, Emma Tabe Eko Niba, Ryo Yabushita, Yoshihiro Bouike, Hisahide Nishio, Hiroyuki Awano
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引用次数: 0

摘要

Ia型糖原储存病(GSDIa,OMIM#223200)是一种常染色体隐性代谢性疾病,其特征是葡萄糖稳态受损,并伴有肝细胞腺瘤/癌的长期并发症。GSDIa是由葡萄糖-6-磷酸酶基因(G6PC)的有害突变引起的。最近的研究表明,通过基因替代疗法进行早期治疗可能是纠正糖代谢和预防严重晚期并发症的良好解决方案。这种疾病的早期治疗需要一个早期疾病检测系统。因此,我们旨在开发一种GSDIa筛查系统,使用干血点(DBS)来检测G6PC中的c.648G>T突变,这是东亚人群中的一种常见突变。在本研究中,共有51个DBS样本(50名健康对照和一名c.648G>T患者)通过改良竞争性寡核苷酸启动PCR(mCOP PCR)进行了检测。在对照DBS样本中,c.648G等位基因在较低的Cq(量化周期)值下扩增(14)。在患者DBS样本中,c.648T等位基因以较低的Cq值扩增(14)。基于这些发现,我们得出结论,我们的mCOP PCR系统清楚地区分了野生型和突变等位基因,并可能适用于筛查G6PC中具有c.648G>T突变的GSDIa。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Glycogen Storage Disease Type Ia Screening Using Dried Blood Spots on Filter Paper: Application of COP-PCR for Detection of the c.648G>T G6PC Gene Mutation.

Glycogen storage disease type Ia (GSDIa, OMIM #232200) is an autosomal recessive metabolic disease characterized by impaired glucose homeostasis and has a long-term complication of hepatocellular adenoma/carcinoma. GSDIa is caused by deleterious mutations in the glucose-6-phosphatase gene (G6PC). Recent studies have suggested that early treatment by gene replacement therapy may be a good solution to correct the glucose metabolism and prevent serious late complications. Early treatment of the disease needs an early disease detection system. Thus, we aimed to develop a screening system for GSDIa using dried blood spots (DBS) to detect the c.648G>T mutation in G6PC, which is a frequent mutation in the East Asian population. In this study, a total of 51 DBS samples (50 healthy controls and one patient with c.648G>T) were tested by modified competitive oligonucleotide priming PCR (mCOP-PCR). In control DBS samples, the c.648G allele was amplified at lower Cq (quantification cycle) values (<11), while the c.648T allele was amplified at higher Cq values (>14). In the patient DBS sample, the c.648T allele was amplified at a lower Cq value (<11), and the c.648G allele was amplified at a higher Cq value (>14). Based on these findings, we concluded that our mCOP-PCR system clearly differentiated the wild-type and mutant alleles, and may be applicable for screening for GSDIa with the c.648G>T mutation in G6PC.

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来源期刊
Kobe Journal of Medical Sciences
Kobe Journal of Medical Sciences Medicine-Medicine (all)
CiteScore
1.20
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0.00%
发文量
4
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