Department of Neurology, West China Hospital of Sichuan University, Chengdu, China.
Acta Neurol Scand. 2019 Mar;139(3):247-253. doi: 10.1111/ane.13046. Epub 2018 Dec 13.
GATOR1 (Gap Activity TOward Rags 1) is composed of three different subunits, DEPDC5 (DEP domain-containing protein 5), NPRL2 (nitrogen permease regulator-like 2) and NPRL3 (nitrogen permease regulator-like 3), and variants in these three genes have mostly been reported in familial focal epilepsy. However, very few studies have been carried out on sporadic drug-resistant focal epilepsy patients. In this study, we aimed to identify the frequency of variants in DEPDC5, NPRL2 and NPRL3 in patients with sporadic drug-resistant focal epilepsy.
MATERIALS & METHODS: One hundred and ninety-three Chinese people with sporadic drug-resistant focal epilepsy were enrolled in the study. Targeted sequencing of DEPDC5, NPRL2 and NPRL3 was applied at an average coverage depth of 2500×.
In the 193 patients with sporadic focal epilepsy included in this study, the median age was 24.6 years with a median age at onset of 13.99 years, and 130 of these patients had identifiable structural lesions. One possibly pathogenic missense variant of DEPDC5, c.2984G>A, p.Arg995His, was found in one patient (0.52%) with hippocampal sclerosis, and one variant of unknown significance, DEPDC5 c.20A>G, p.Tyr7Cys, was found in two patients with hippocampal sclerosis (1.04%).
Our findings suggested that DEPDC5 might be of more importance than NPRL2 or NPRL3 in Chinese epilepsy patients with sporadic drug-resistant focal epilepsy. Future research should focus on the mechanism by which the mechanistic target of rapamycin (mTOR) is involved in epileptogenesis in sporadic epilepsy.
GATOR1(Gap Activity TOward Rags 1)由三个不同的亚基组成,DEP DC5(DEP 结构域蛋白 5)、NPRL2(氮渗透调节蛋白类似物 2)和 NPRL3(氮渗透调节蛋白类似物 3),这些基因的变异主要在家族性局灶性癫痫中报道。然而,很少有研究针对散发性耐药性局灶性癫痫患者进行。在这项研究中,我们旨在鉴定 DEPDC5、NPRL2 和 NPRL3 变异在散发性耐药性局灶性癫痫患者中的频率。
本研究纳入 193 例中国散发性耐药性局灶性癫痫患者。应用靶向测序技术对 DEPDC5、NPRL2 和 NPRL3 进行测序,平均覆盖深度为 2500×。
在本研究纳入的 193 例散发性局灶性癫痫患者中,中位年龄为 24.6 岁,中位发病年龄为 13.99 岁,其中 130 例患者有可识别的结构性病变。在一名伴有海马硬化的患者(0.52%)中发现 DEPDC5 基因的一个可能致病的错义变异 c.2984G>A,p.Arg995His,在两名伴有海马硬化的患者中发现一个未知意义的变异 DEPDC5 c.20A>G,p.Tyr7Cys(1.04%)。
我们的研究结果表明,DEPDC5 在伴有散发性耐药性局灶性癫痫的中国癫痫患者中可能比 NPRL2 或 NPRL3 更为重要。未来的研究应集中在雷帕霉素靶蛋白(mTOR)在散发性癫痫中参与癫痫发生的机制上。