Shiva Mahsa, Hosseinpour Sareh, Ashrafi Mahmoud Reza, Heidari Morteza, Rezaei Zahra, Zebardast Jayran, Mohammadpour Masoud, Bonkowsky Joshua L, Tavasoli Ali Reza
Myelin Disorders Clinic, Pediatric Neurology Division, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran.
Department of Pediatric Neurology, Vali-E-Asa Hospital, Tehran University of Medical Sciences, Tehran, Iran.
J Child Neurol. 2025 Apr;40(4):233-240. doi: 10.1177/08830738241293171. Epub 2024 Nov 18.
Leukodystrophies are a heterogeneous group of inherited neurologic disorders. These disorders are indeed progressive and debilitating conditions with limited treatment options and high mortality rates. There is a deficiency in available data concerning both the mortality rates and the most common causes of death in leukodystrophies. We investigated the mortality rates, mean age at death, and the most common causes of death in a retrospective cohort of 165 Iranian pediatric patients who were diagnosed with leukodystrophies. Death was recorded in 64 of 165 patients (38.8%) with a mean follow-up of 4.7 ± 3.25 years. The mean age of living patients was 7.9 ± 4.8 years and the mean age at death was 5.2 ± 3.9 years. Mortality rate of the entire cohort was 18.1% (30/165), 24.2% (40/165), and 35.7% (59/165) at 3, 5, and 10 years' follow-up, respectively. The mean age at death was 2.13 ± 0.68 years, 2.67 ± 1.14 years, and 4.33 ± 2.73 years, at 3-, 5-, and 10-year follow-up from first symptom onset, correspondingly. However, there was a significant difference in the mean age at death in years in hypomyelinating leukodystrophies compared with other leukodystrophies (2.19 0.19 standard error [SE], confidence interval [CI] 1.81-2.56; and 6.65 ± 0.62 SE (CI 5.42-7.87); log rank = .0001, analysis of variance = .0001). The most common causes of death were cardiopulmonary problems (47%), seizures (11%), sepsis (9%), and miscellaneous (33%). We proposed that a significant majority of childhood leukodystrophy deaths occur within the first 5 years of life, with a notable concentration during the initial 3 years. Further, the results of this study suggest the potential for targeted strategies to address the specific causes of death in children with leukodystrophies.
脑白质营养不良是一组遗传性神经系统疾病,具有异质性。这些疾病确实是进行性且使人衰弱的病症,治疗选择有限且死亡率高。关于脑白质营养不良的死亡率和最常见死因,现有数据不足。我们对165例被诊断为脑白质营养不良的伊朗儿科患者进行回顾性队列研究,调查其死亡率、平均死亡年龄和最常见死因。165例患者中有64例(38.8%)死亡,平均随访时间为4.7±3.25年。存活患者的平均年龄为7.9±4.8岁,平均死亡年龄为5.2±3.9岁。整个队列在3年、5年和10年随访时的死亡率分别为18.1%(30/165)、24.2%(40/165)和35.7%(59/165)。从首次出现症状开始,在3年、5年和10年随访时的平均死亡年龄分别为2.13±0.68岁、2.67±1.14岁和4.33±2.73岁。然而,与其他脑白质营养不良相比,低髓鞘性脑白质营养不良的平均死亡年龄存在显著差异(2.19±0.19标准误[SE],置信区间[CI]1.81 - 2.56;以及6.65±0.62 SE(CI 5.42 - 7.87);对数秩检验 = 0.0001,方差分析 = 0.0001)。最常见的死因是心肺问题(47%)、癫痫发作(11%)、败血症(9%)和其他(33%)。我们提出,绝大多数儿童脑白质营养不良死亡发生在生命的前5年,在最初3年尤为集中。此外,本研究结果表明有可能制定针对性策略来解决脑白质营养不良儿童的具体死因。