Tsai Fang-Chih, Lee Han-Jui, Wang An-Guor, Hsieh Shu-Chen, Lu Yung-Hsiu, Lee Ming-Che, Pai Ju-Shan, Chu Tzu-Hung, Yang Chia-Feng, Hsu Ting-Rong, Lai Chih-Jou, Tsai Ming-Tzu, Ho Ping-Hsun, Lin Min-Chieh, Cheng Ling-Yee, Chuang Ya-Chin, Niu Dau-Ming
Department of Pediatrics, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan, ROC; School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.
J Chin Med Assoc. 2017 Apr;80(4):253-261. doi: 10.1016/j.jcma.2016.07.006. Epub 2017 Mar 13.
Glutaric aciduria type 1 (GA-1) is an organic acidemia with potentially severe neurological sequelae. In Taiwan, newborn screening (NBS) for GA-1 began in 2001, but large-scale reporting is lacking. This study describes Taiwan's largest newborn screening population to date.
Between 2001 and 2015, 1,490,636 newborns were screened for GA-1. Confirmatory examinations included the carnitine loading test. Confirmed patients were treated with a low lysine diet, carnitine, and high-energy intake during illness. Clinical, laboratory, and neuroimaging data were analyzed.
Fourteen newborns were diagnosed with GA-1 (incidence: 1/106,474). C5DC concentration was clearly increased after carnitine loading in the affected newborns, but not in false-positive newborns (p = 0.004), indicating that this test is useful as an adjuvant diagnostic method. Eleven patients followed in our hospital were enrolled, namely nine NBS patients and two patients diagnosed clinically. IVS10-2A>C was the most common mutation. Two novel mutations (T36fs and N291K) were identified. Pendular nystagmus was found in two pediatric GA-1 patients. The corresponding pathology was optic atrophy in one patient, but remained undetermined in the other patient. The frequency of encephalopathic crisis decreased substantially following NBS. Among patients diagnosed by NBS, cognitive functioning was better among patients with good compliance than patients with poor compliance (p = 0.03). Abnormalities were detected by brain MRI including diffusion-weighted imaging and apparent diffusion coefficient maps; these affected various brain regions at different stages of the disease. Basal ganglion injuries occurred after an encephalopathic crisis. White matter disease was prevalent among older patients, either with or without an encephalopathic crisis.
Early diagnosis by newborn screening followed by full compliance with treatment guidelines is important to a good outcome.
1型戊二酸血症(GA - 1)是一种有机酸血症,可能伴有严重的神经后遗症。在台湾,GA - 1的新生儿筛查始于2001年,但缺乏大规模报告。本研究描述了台湾迄今为止最大规模的新生儿筛查人群。
2001年至2015年期间,对1,490,636名新生儿进行了GA - 1筛查。确诊检查包括肉碱负荷试验。确诊患者在患病期间接受低赖氨酸饮食、肉碱和高能量摄入治疗。对临床、实验室和神经影像学数据进行了分析。
14名新生儿被诊断为GA - 1(发病率:1/106,474)。受影响新生儿在肉碱负荷后C5DC浓度明显升高,而假阳性新生儿则无此现象(p = 0.004),表明该试验作为辅助诊断方法很有用。我们医院随访的11名患者被纳入研究,其中9名是通过新生儿筛查确诊的患者,2名是临床诊断的患者。IVS10 - 2A>C是最常见的突变。鉴定出两个新突变(T36fs和N291K)。两名儿童GA - 1患者出现摆动性眼球震颤。其中一名患者相应病理为视神经萎缩,另一名患者病理未明确。新生儿筛查后脑病危机的发生率大幅下降。在通过新生儿筛查确诊的患者中,依从性好的患者认知功能优于依从性差的患者(p = 0.03)。脑部MRI检查发现异常,包括弥散加权成像和表观扩散系数图;这些异常在疾病的不同阶段影响不同脑区。基底神经节损伤发生在脑病危机之后。白质病在老年患者中普遍存在,无论有无脑病危机。
通过新生儿筛查进行早期诊断并完全遵循治疗指南对良好预后很重要。