Tsai Meng-Ju Melody, Chang Jung-Chi, Lu Heng-Yu, Gau Susan Shur-Fen, Chien Yin-Hsiu, Hwu Wuh-Liang, Ni Yen-Hsuan, Chen Huey-Ling, Lee Ni-Chung
Department of Pediatrics, National Taiwan University Hospital and College of Medicine, National Taiwan University, Taipei, Taiwan.
Department of Pediatrics, National Taiwan University Hospital Yunlin Branch, Yunlin, Taiwan.
Clin Exp Pediatr. 2025 Mar;68(3):257-265. doi: 10.3345/cep.2024.01102. Epub 2024 Nov 28.
Citrin deficiency is a rare metabolic disorder prevalent in East and Southeast Asia that affects liver or neurological function throughout various life stages. While early diagnosis and dietary management can improve prognosis for infant onset disease, data on long-term neurocognitive outcomes is scarce.
This study aimed to clarify whether transient metabolic disturbances during early childhood have a lasting effect on the neurocognitive function of individuals with citrin deficiency.
Thirty patients diagnosed with citrin deficiency prior to 1 year of age underwent neuropsychological assessments including attention deficit/hyperactivity disorders (ADHD) and intelligence quotient (IQ). We compared the peak laboratory values during infancy between children who were versus were not later diagnosed with ADHD.
Neurocognitive assessments of 30 individuals with citrin deficiency aged 3-25 years revealed that full-scale IQ scores were normally distributed. Of this cohort, 47% (14 of 30) were diagnosed with ADHD: 6, 6, and 2 with the combined, inattentive, and hyperactive-impulsive types, respectively. This prevalence was higher than that in the general population (1.7%-16%). Moreover, a one-unit increase in ammonia levels before 1 year of age was associated with a 1.023-fold increase in the likelihood of future hyperactivity-impulsivity symptoms (P=0.038; 95%confidence interval, 1.001-1.046). Despite these findings, this long-term follow-up of individuals with citrin deficiency indicated that it had minimal impact on neurocognitive function, allowing for a generally normal life.
Patients with a history of cholestasis caused by citrin deficiency during infancy have a greater incidence of ADHD than the general population, suggesting that metabolic disturbances during early childhood in individuals with citrin deficiency may have a long-term negative impact on their neurocognitive function.
瓜氨酸缺乏症是一种罕见的代谢紊乱疾病,在东亚和东南亚地区较为普遍,会在生命的各个阶段影响肝脏或神经功能。虽然早期诊断和饮食管理可以改善婴儿期发病疾病的预后,但关于长期神经认知结果的数据却很稀少。
本研究旨在阐明幼儿期短暂的代谢紊乱是否会对瓜氨酸缺乏症患者的神经认知功能产生持久影响。
30例在1岁前被诊断为瓜氨酸缺乏症的患者接受了神经心理学评估,包括注意力缺陷多动障碍(ADHD)和智商(IQ)测试。我们比较了后来被诊断出患有ADHD和未被诊断出患有ADHD的儿童在婴儿期的实验室峰值数据。
对30名年龄在3至25岁的瓜氨酸缺乏症患者进行的神经认知评估显示,全量表智商得分呈正态分布。在这个队列中,47%(30人中的14人)被诊断患有ADHD:其中6人、6人、2人分别为混合型、注意力不集中型和多动冲动型。这一患病率高于一般人群(1.7%-16%)。此外,1岁前氨水平每增加一个单位,未来出现多动冲动症状的可能性就增加1.023倍(P=0.038;95%置信区间,1.001-1.046)。尽管有这些发现,但对瓜氨酸缺乏症患者的长期随访表明,它对神经认知功能的影响最小,患者通常可以过上正常生活。
婴儿期因瓜氨酸缺乏引起胆汁淤积病史的患者患ADHD的发生率高于一般人群,这表明瓜氨酸缺乏症患者幼儿期的代谢紊乱可能会对其神经认知功能产生长期负面影响。