Department of Community Medicine and Social Healthcare Science, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe, Hyogo 650-0017, Japan.
Faculty of Nutrition, Kobe Gakuin University, 518 Arise, Ikawadani-cho, Nishi-ku, Kobe, Hyogo 651-2180, Japan.
Kobe J Med Sci. 2021 Nov 2;67(2):E71-E78.
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.
糖原贮积病 Ia 型(GSDIa,OMIM#232200)是一种常染色体隐性遗传代谢疾病,其特征为葡萄糖稳态受损,并伴有肝细胞腺瘤/癌这一长期并发症。GSDIa 由葡萄糖-6-磷酸酶基因(G6PC)的有害突变引起。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葡萄糖代谢并预防严重晚期并发症的一个好方法。疾病的早期治疗需要一个早期的疾病检测系统。因此,我们旨在使用干血斑(DBS)开发一种用于 GSDIa 的筛查系统,以检测 G6PC 中的 c.648G>T 突变,这是东亚人群中的一种常见突变。在这项研究中,总共测试了 51 个 DBS 样本(50 个健康对照和一个患有 c.648G>T 的患者),采用改良竞争寡核苷酸引物 PCR(mCOP-PCR)进行检测。在对照 DBS 样本中,c.648G 等位基因的扩增 Cq 值(定量循环)较低(<11),而 c.648T 等位基因的扩增 Cq 值较高(>14)。在患者的 DBS 样本中,c.648T 等位基因的扩增 Cq 值较低(<11),而 c.648G 等位基因的扩增 Cq 值较高(>14)。基于这些发现,我们得出结论,我们的 mCOP-PCR 系统能够清楚地区分野生型和突变型等位基因,可能适用于筛查 G6PC 中的 c.648G>T 突变导致的 GSDIa。