Characterization of Adult Patients With Neurometabolic Disorders: A Cross-Sectional Study at a Tertiary Neurology Center in Sweden

IF 1.8 Q2 Biochemistry, Genetics and Molecular Biology
JIMD reports Pub Date : 2026-08-01 DOI:10.1002/jmd2.70115
Boel Ernerdahl, Ashraf Yahia, Andreas Puschmann
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Abstract

Adult patients with inherited metabolic diseases are often overlooked. Limited data on this population hinder adequate planning of their clinical and social care. In this retrospective, observational, cross-sectional service evaluation study, we reviewed the electronic medical records of adult patients with inherited neurometabolic diseases (NIMD) managed at Skåne University Hospital between 2020 and 2024. Skåne University Hospital, located in Region Skåne in Southern Sweden, is one of three specialized tertiary centers for inherited metabolic diseases in Sweden. The aim of this study was to characterize these patients demographically and clinically and to describe their treatment profiles, functional status, and social support. We identified 59 patients. Most patients had disorders of intermediary energy metabolism (21/59; 35.6%) or lipid metabolism (14/59; 23.7%), including 10 patients (16.9%) with adrenoleukodystrophy. Disease-specific treatments were provided to 65.4% of patients, and 83.6% were under continuous follow-up. Sixteen patients (27.1%) were fully independent, lived in their own homes, did not require societal support nor mobility aid, and worked/studied full time/retired due to old age. More than half of the patients (50.8%) received no disability or social support. In conclusion, adult patients with NIMD represent a heterogeneous group with variable clinical and social needs. Despite the rarity of individual NIMDs, disease-specific treatments were commonly used in our center. Further studies, particularly long-term follow-up studies, are required to better understand NIMD clinical trajectories and to optimize both medical management and social support for adults with NIMD.

Abstract Image

成年神经代谢紊乱患者的特征:瑞典三级神经病学中心的横断面研究
成人遗传性代谢性疾病患者往往被忽视。关于这一人群的有限数据妨碍了对其临床和社会护理的充分规划。在这项回顾性、观察性、横断面服务评估研究中,我们回顾了sk大学医院在2020年至2024年间管理的患有遗传性神经代谢性疾病(NIMD)的成年患者的电子病历。skamatne大学医院位于瑞典南部skamatne地区,是瑞典遗传代谢疾病的三个专业三级中心之一。本研究的目的是对这些患者的人口学和临床特征进行描述,并描述他们的治疗概况、功能状态和社会支持。我们确定了59例患者。大多数患者存在中间能量代谢障碍(21/59;35.6%)或脂质代谢障碍(14/59;23.7%),其中肾上腺脑白质营养不良10例(16.9%)。65.4%的患者接受了疾病特异性治疗,83.6%的患者接受了持续随访。16名患者(27.1%)完全独立,住在自己的家中,不需要社会支持或行动援助,全职工作/学习/因年老而退休。超过一半(50.8%)的患者未获得残疾或社会支持。综上所述,NIMD成年患者是一个异质性群体,具有不同的临床和社会需求。尽管个体nimd罕见,但我们中心通常使用针对疾病的治疗方法。需要进一步的研究,特别是长期随访研究,以更好地了解NIMD的临床轨迹,并优化对患有NIMD的成人的医疗管理和社会支持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JIMD reports
JIMD reports Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
CiteScore
3.30
自引率
0.00%
发文量
84
审稿时长
12 weeks
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