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一项基于人群的杜氏肌营养不良症严重、罕见合并症研究。

A population-based study of severe, less common comorbidities in Duchenne muscular dystrophy.

作者信息

Wahlgren Lisa, Nordström Sara, Tulinius Már, Kroksmark Anna-Karin, Sofou Kalliopi

机构信息

Department of Pediatrics, Institute of Clinical Sciences, University of Gothenburg, Gothenburg, Sweden.

The Queen Silvia Children's Hospital, Sahlgrenska University Hospital, Member of the European Reference Network EURO-NMD, Gothenburg, Sweden.

出版信息

J Neurol. 2025 Aug 28;272(9):596. doi: 10.1007/s00415-025-13323-6.

DOI:10.1007/s00415-025-13323-6
PMID:40874969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12394381/
Abstract

BACKGROUND

Since the increasing longevity and the advent of new therapeutic modalities in Duchenne muscular dystrophy (DMD), comprehensive clinical surveillance is of paramount importance. Our study aimed to examine the occurrence of severe, less common comorbidities among patients with DMD and their impact on life expectancy and overall disease burden.

METHODS

This was a retrospective, nationwide study of all male patients with DMD who were followed at a medical clinic in Sweden, born and deceased during the period 1970-2019. Data regarding cause-of-death and comorbidities were retrieved by the medical records and the Cause of death Registry. The assessed variables were defined as 'severe' when depicting comorbidities with potentially serious, life-threatening outcomes.

RESULTS

Of the 129 included patients, approximately 56% presented with at least one severe complication or event, the most common being gastrointestinal complications and life-threatening arrhythmias, with incidence rates of 56.8 and 48.3/10,000 person-years, respectively. Acute kidney injury with an incidence of 16.6/10,000 person-years, was primarily seen within the months preceding death. Vascular events occurred in 10.7% of the patients, mainly cerebrovascular events and venous thromboembolism -including fatal post-traumatic pulmonary embolism-, each with an incidence of 23.5/10,000 person-years. Fracture occurrence, predominantly seen among non-ambulatory patients, had an incidence of 310/10,000 person-years. We further studied cumulative incidences and associations with loss of ambulation and glucocorticoids.

CONCLUSION

Our study provides new insights into severe comorbidities in DMD, emphasizing the need for lifelong disease monitoring, especially considering that many complications are subject to prevention and, if detected early, to successful treatment.

摘要

背景

随着杜氏肌营养不良症(DMD)患者寿命的延长以及新治疗方式的出现,全面的临床监测至关重要。我们的研究旨在调查DMD患者中严重、较少见的合并症的发生情况及其对预期寿命和总体疾病负担的影响。

方法

这是一项对瑞典一家诊所随访的所有男性DMD患者进行的回顾性全国性研究,这些患者在1970年至2019年期间出生和死亡。通过病历和死因登记处获取有关死因和合并症的数据。当描述具有潜在严重、危及生命后果的合并症时,评估变量被定义为“严重”。

结果

在129名纳入患者中,约56%至少出现一种严重并发症或事件,最常见的是胃肠道并发症和危及生命的心律失常,发病率分别为56.8/10000人年和48.3/10000人年。急性肾损伤的发病率为16.6/10000人年,主要出现在死亡前几个月。10.7%的患者发生血管事件,主要是脑血管事件和静脉血栓栓塞——包括致命的创伤后肺栓塞——每种事件的发病率均为23.5/10000人年。骨折主要发生在非卧床患者中,发病率为310/10000人年。我们进一步研究了累积发病率以及与行走能力丧失和糖皮质激素的关联。

结论

我们的研究为DMD的严重合并症提供了新的见解,强调了终身疾病监测的必要性,特别是考虑到许多并发症是可以预防的,并且如果早期发现,可以成功治疗。

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本文引用的文献

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Incidence of Radiologically Confirmed Fractures in Adults With Duchenne Muscular Dystrophy.杜氏肌营养不良症成年患者中经放射学确诊的骨折发生率
Muscle Nerve. 2025 Apr;71(4):558-563. doi: 10.1002/mus.28355. Epub 2025 Jan 23.
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Delivery of genetic medicines for muscular dystrophies.用于治疗肌肉萎缩症的基因药物递送
Cell Rep Med. 2025 Jan 21;6(1):101885. doi: 10.1016/j.xcrm.2024.101885. Epub 2025 Jan 6.
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Long-Term Use of Oral Corticosteroids and Safety Outcomes for Patients With Atopic Dermatitis.长期使用口服皮质类固醇治疗特应性皮炎的安全性结局。
JAMA Netw Open. 2024 Jul 1;7(7):e2423563. doi: 10.1001/jamanetworkopen.2024.23563.
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Disease-associated comorbidities, medication records and anthropometric measures in adults with Duchenne muscular dystrophy.杜氏肌营养不良症成年患者的疾病相关合并症、用药记录和人体测量学指标。
Neuromuscul Disord. 2024 Aug;41:8-19. doi: 10.1016/j.nmd.2024.05.007. Epub 2024 May 14.
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Severe gastrointestinal problems in Duchenne muscular dystrophy: A case series.Duchenne 型肌营养不良症的严重胃肠道问题:病例系列。
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