Long-term follow-up of neurocognitive function in patients with citrin deficiency and cholestasis.

IF 3.2 Q1 PEDIATRICS Clinical and Experimental Pediatrics Pub Date : 2024-11-28 DOI:10.3345/cep.2024.01102
Meng-Ju Melody Tsai, Jung-Chi Chang, Heng-Yu Lu, Susan Shur-Fen Gau, Yin-Hsiu Chien, Wuh-Liang Hwu, Yen-Hsuan Ni, Huey-Ling Chen, Ni-Chung Lee
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Abstract

Background: 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.

Purpose: 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.

Methods: Thirty patients diagnosed with citrin deficiency prior to 1 year of age underwent neuropsychological assessments including attention-deficit/hyperactivity disorder (ADHD) and intelligence quotient (IQ). We compared the peak laboratory values during infancy between children who were versus were not later diagnosed with ADHD.

Results: 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: six, six, and two 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.

Conclusion: 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.

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柠檬素缺乏和胆汁淤积症患者神经认知功能的长期随访。
背景:柠檬素缺乏症是一种罕见的代谢性疾病,普遍存在于东亚和东南亚,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发病疾病的预后,但关于长期神经认知结果的数据很少。目的:本研究旨在阐明儿童早期短暂的代谢紊乱是否对柠檬素缺乏症患者的神经认知功能有持久的影响。方法:30例1岁前诊断为柠檬素缺乏症的患者进行了神经心理学评估,包括注意缺陷/多动障碍(ADHD)和智商(IQ)。我们比较了婴儿期被诊断为ADHD的儿童和未被诊断为ADHD的儿童的实验室峰值值。结果:对30例年龄在3 ~ 25岁的柠檬素缺乏症患者进行神经认知测试,结果显示其全量表IQ得分呈正态分布。在这个队列中,47%(30人中有14人)被诊断为多动症:分别有6人、6人、2人患有混合型、注意力不集中型和多动冲动型。该患病率高于普通人群(1.7-16%)。此外,1岁前氨水平每增加1个单位,未来出现多动冲动症状的可能性增加1.023倍(p = 0.038;95%置信区间为1.001-1.046)。尽管有这些发现,但对柠檬素缺乏症患者的长期随访表明,它对神经认知功能的影响很小,可以维持正常的生活。结论:婴儿期有柠檬酸缺乏症引起的胆汁淤积史的患者ADHD的发生率高于一般人群,提示儿童早期柠檬酸缺乏症患者的代谢紊乱可能对其神经认知功能产生长期的负面影响。
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来源期刊
CiteScore
8.00
自引率
2.40%
发文量
88
审稿时长
60 weeks
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