Kehrer Christiane, Bevot Andrea, Martin Pascal, Raabe Christa, Gregor Saskia, Krägeloh-Mann Ingeborg, Groeschel Samuel
Department of Paediatric Neurology and Developmental Medicine, University Children'S Hospital, Hoppe-Seyler-Straße 1, 72076, Tübingen, Germany.
Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tuebingen, 72076, Tübingen, Germany.
Orphanet J Rare Dis. 2025 May 23;20(1):242. doi: 10.1186/s13023-025-03637-z.
Metachromatic leukodystrophy (MLD) is a life-limiting neurodegenerative disease due to pathogenic variants in the ARSA gene. Patients experience severe neurological symptoms, developmental regression, and early death. Aim of the study was to analyze disease burden and healthcare utilization in different stages of the disease in children with late infantile and juvenile MLD in Germany.
Out of a nationwide total cohort study (TC) (n = 83), we undertook telephone interviews in a representative follow-up cohort (FC) defined by advanced disease stages (n = 19). The FC allowed detailed long-term data of the disease in addition to cross-sectional data of the TC.
Nearly all patients showed spasticity, truncal hypotonia and dysphagia, and about half of the patients developed epilepsy. Most children required special education; none finished regular school. Analysis of the FC showed that neuronal intestinal burden was extensive, including obstipation (57%), micturition problems (47%), and tube feeding (63%). Gallbladder polyposis was seen in 52%. General well-being did not strongly correlate with motor function, whereas pain was associated with reduced well-being. Baclofen, Omeprazole, Vigabatrin and Polyethyleneglycol were the most frequently used drugs. Patients took up to 15 different drugs daily. Altogether, 127 hospitalisations (485 treatment days) were registered in the FC (median age 9 years, median one inpatient stay per patient per year). Diagnostic procedures were main reasons for hospitalization (29 hospitalizations, 128 treatment days), and accounted for the main burden for families (68%). The median use of 15 different devices (maximum 29) throughout life illustrated a high burden of the disease. During disease course, there was a change from more "active" devices (e.g., walker) to more "passive" devices (e.g., form seat). Physical therapy was the most relevant therapy in advanced disease stages (100%), while occupational therapy or speech therapy primarily were used in early disease stages. State welfare benefits, home- and palliative care were used broadly.
Diagnostic and treatment routine pathways and sociomedical support in MLD require extensive resources. We provide detailed cross-sectional and long-term data of MLD-associated disease burden in different stages of disease. This data may serve as a reference when analyzing disease- and healthcare burden also after gene-/stem cell-therapy.
异染性脑白质营养不良(MLD)是一种由ARSA基因突变导致的致命性神经退行性疾病。患者会出现严重的神经症状、发育倒退并过早死亡。本研究旨在分析德国晚发性婴儿型和青少年型MLD患儿疾病不同阶段的疾病负担及医疗资源利用情况。
在一项全国性队列研究(TC)(n = 83)中,我们对一个由疾病晚期定义的代表性随访队列(FC)(n = 19)进行了电话访谈。除了TC的横断面数据外,FC还提供了该疾病详细的长期数据。
几乎所有患者都表现出痉挛、躯干肌张力减退和吞咽困难,约一半患者出现癫痫。大多数儿童需要特殊教育;无人完成正规学业。对FC的分析显示,神经肠道负担广泛,包括便秘(57%)、排尿问题(47%)和鼻饲(63%)。52%的患者有胆囊息肉。总体健康状况与运动功能没有强烈相关性,而疼痛与健康状况下降有关。巴氯芬、奥美拉唑、氨己烯酸和聚乙二醇是最常用的药物。患者每天服用多达15种不同药物。FC队列共记录了127次住院(485个治疗日)(中位年龄9岁,每位患者每年中位住院1次)。诊断程序是住院的主要原因(29次住院,128个治疗日),也是家庭的主要负担(68%)。患者一生中平均使用15种不同设备(最多29种),表明疾病负担较重。在疾病过程中,使用的设备从更多“主动”型(如助行器)转变为更多“被动”型(如成型座椅)。物理治疗是疾病晚期最主要的治疗方式(100%),而职业治疗或言语治疗主要用于疾病早期。国家福利、居家和姑息治疗广泛应用。
MLD的诊断和治疗常规路径以及社会医疗支持需要大量资源。我们提供了MLD在疾病不同阶段相关疾病负担的详细横断面和长期数据。这些数据在分析基因/干细胞治疗后的疾病和医疗负担时可作为参考。