Laboratory of Molecular Biology, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16147 Genova, Italy.
Clinical Bioinformatics Unit, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16147 Genova, Italy.
Int J Mol Sci. 2021 Dec 28;23(1):328. doi: 10.3390/ijms23010328.
Glycogen storage disease type Ia (GSDIa) is an inherited metabolic disorder caused by mutations in the enzyme glucose-6-phosphatase-α (G6Pase-α). Affected individuals develop renal and liver complications, including the development of hepatocellular adenoma/carcinoma and kidney failure. The purpose of this study was to identify potential biomarkers of the evolution of the disease in GSDIa patients. To this end, we analyzed the expression of exosomal microRNAs (Exo-miRs) in the plasma exosomes of 45 patients aged 6 to 63 years. Plasma from age-matched normal individuals were used as controls. We found that the altered expression of several Exo-miRs correlates with the pathologic state of the patients and might help to monitor the progression of the disease and the development of late GSDIa-associated complications.
糖原贮积病 Ia 型(GSDIa)是一种由葡萄糖-6-磷酸酶-α(G6Pase-α)酶基因突变引起的遗传性代谢紊乱。受影响的个体会出现肾脏和肝脏并发症,包括肝细胞腺瘤/癌和肾衰竭的发展。本研究的目的是确定 GSDIa 患者疾病进展的潜在生物标志物。为此,我们分析了 45 名年龄在 6 至 63 岁的患者血浆外泌体中的外泌体 microRNAs(Exo-miRs)的表达。使用年龄匹配的正常个体的血浆作为对照。我们发现,几种 Exo-miRs 的改变表达与患者的病理状态相关,可能有助于监测疾病的进展和晚期 GSDIa 相关并发症的发生。