代谢性疾病肝移植术后的长期神经发育结果--单一中心的经验。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Journal of Inherited Metabolic Disease Pub Date : 2024-08-12 DOI:10.1002/jimd.12785
Catherine Patterson, Anna Gold, Stephanie So, Leila Kahnami, Michaela Dworsky-Fried, Eva Mamak, Alaine Rogers, Andreas Schulze, Birgit Ertl-Wagner, Vicky Ng, Yaron Avitzur
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引用次数: 0

摘要

本研究描述了尿素循环障碍(UCD)和有机酸血症(OA)患儿在肝移植(LT)前、肝移植后 1 年和 3 年的神经发育结果。我们对2014年1月至2021年12月期间移植的OA或UCD患儿进行了回顾性病历审查。我们收集了在任何时间点进行过≥1次运动/认知评估的儿童的标准化运动和认知评估得分。LT前脑磁共振成像(MRI)进行了分级。研究还探讨了人口统计学/医学变量与神经发育结果之间的关联。26名儿童(64%为男性)在中位年龄1.4岁(四分位距为0.71-3.84)时接受了LT治疗。15名患儿(58%)确诊为尿毒症,14名患儿(54%)因高氨血症需要透析,10名患儿(42%)在确诊前有典型的癫痫发作。在各个时间点,大运动量评分低于平均值大于 1 个标准差 (SD) 的儿童比例有所增加,在各个时间点,智力评分低于平均值大于 2 个标准差的儿童比例≥50%。我们注意到以下重要关联:UCD 诊断与较低的一般智力评分有关(p = 0.019);精琥珀酸裂解酶缺乏症诊断与长管治疗后 3 年较低的视觉运动评分有关(p = 0.035);长管治疗前有癫痫发作史与长管治疗后 3 年较低的一般智力(低于平均值 2SD 以上)有关(p = 0.020);LT 前有透析史,LT 后 1 年时运动评分较低(低于平均值 1 SD 以上)(p = 0.039);LT 前有癫痫发作史,LT 后 3 年时一般智力评分较高(p = 0.001)。磁共振成像分级与发育评分无关。在我们的单中心研究中,与人群标准相比,患有UCD或OA的儿童在LT后出现发育障碍的比例更高。早期筛查、先期移植和康复治疗可优化长期预后。
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Long-term neurodevelopmental outcomes following liver transplantation for metabolic disease-a single centre experience.

This study describes the neurodevelopmental outcome of children with urea cycle disorders (UCD) and organic acidemias (OA) preliver transplant (LT), 1-year, and 3-years post-LT. We performed a retrospective chart review of children with OA or UCD transplanted between January 2014 and December 2021. Standardized motor and cognitive assessment scores were collected from children who had ≥1 motor/cognitive assessment at any timepoint. Pre-LT brain magnetic resonance imaging (MRI) was graded. Associations between demographic/medical variables and neurodevelopmental outcomes were explored. Twenty-six children (64% male) underwent LT at a median age of 1.4 (interquartile range 0.71, 3.84) years. Fifteen (58%) had a UCD diagnosis, 14 (54%) required dialysis for hyperammonemia, and 10 (42%) had seizures typically around diagnosis. The proportion of children with gross motor scores >1 standard deviation (SD) below the mean increased across timepoints, and ≥50% demonstrated general intellect scores >2 SD below the mean at each timepoint. The following significant associations were noted: UCD diagnoses with lower general intellect scores (p = 0.019); arginosuccinate lyase deficiency diagnosis with lower visual motor scores at 3-years post-LT (p = 0.035); a history of seizures pre-LT with lower general intellect (>2SD below the mean) at 3-years post-LT (p = 0.020); dialysis pre-LT with lower motor scores (>1 SD below the mean) at 1-year post-LT (p = 0.039); pre-emptive LT with higher general intellect scores at 3-years post-LT (p = 0.001). MRI gradings were not associated with developmental scores. In our single centre study, children with UCD or OA had a higher prevalence of developmental impairment post-LT compared to population norms. Earlier screening, pre-emptive transplant, and rehabilitation may optimize long-term outcomes.

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来源期刊
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease 医学-内分泌学与代谢
CiteScore
9.50
自引率
7.10%
发文量
117
审稿时长
4-8 weeks
期刊介绍: The Journal of Inherited Metabolic Disease (JIMD) is the official journal of the Society for the Study of Inborn Errors of Metabolism (SSIEM). By enhancing communication between workers in the field throughout the world, the JIMD aims to improve the management and understanding of inherited metabolic disorders. It publishes results of original research and new or important observations pertaining to any aspect of inherited metabolic disease in humans and higher animals. This includes clinical (medical, dental and veterinary), biochemical, genetic (including cytogenetic, molecular and population genetic), experimental (including cell biological), methodological, theoretical, epidemiological, ethical and counselling aspects. The JIMD also reviews important new developments or controversial issues relating to metabolic disorders and publishes reviews and short reports arising from the Society''s annual symposia. A distinction is made between peer-reviewed scientific material that is selected because of its significance for other professionals in the field and non-peer- reviewed material that aims to be important, controversial, interesting or entertaining (“Extras”).
期刊最新文献
News from Valencia: JIMD themed issue on ureagenesis defects and allied disorders. The relation between dietary polysaccharide intake and urinary excretion of tetraglucoside. Nontargeted urine metabolomic analysis of acute intermittent porphyria reveals novel interactions between bile acids and heme metabolism: New promising biomarkers for the long-term management of patients. Exploring RNA therapeutics for urea cycle disorders. Therapeutic liver cell transplantation to treat murine PKU.
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