Dysarthria and dysphagia in patients with mitochondrial diseases

IF 3.7 2区 生物学 Q2 ENDOCRINOLOGY & METABOLISM Molecular genetics and metabolism Pub Date : 2024-06-01 DOI:10.1016/j.ymgme.2024.108510
R.E.M. Kuin , J.T. Groothuis , P. Buit , M.C.H. Janssen , S. Knuijt
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Abstract

Background

Information about dysarthria and dysphagia in mitochondrial diseases (MD) is scarce. However, this knowledge is needed to identify speech and swallowing problems early, to monitor the disease course, and to develop and offer optimal treatment and support. This study therefore aims to examine the prevalence and severity of dysarthria and dysphagia in patients with MD and its relation to clinical phenotype and disease severity. Secondary aim is to determine clinically relevant outcome measures for natural history studies and clinical trials.

Methods

This retrospective cross-sectional medical record study includes adults (age ≥ 18 years) diagnosed with genetically confirmed MD who participated in a multidisciplinary admission within the Radboud center for mitochondrial medicine between January 2015 and April 2023. Dysarthria and dysphagia were examined by administering the Radboud dysarthria assessment, swallowing speed, dysphagia limit, test of mastication and swallowing solids (TOMASS), and 6-min mastication test (6MMT). The disease severity was assessed using the Newcastle mitochondrial disease scale for adults (NMDAS).

Results

The study included 224 patients with MD with a median age of 42 years of whom 37.5% were male. The pooled prevalence of dysarthria was 33.8% and of dysphagia 35%. Patients with MD showed a negative deviation from the norm on swallowing speed, TOMASS (total time) and the 6MMT. Furthermore, a significant moderate relation was found between the presence of dysarthria and the clinical phenotypes. There was a statistically significant difference in total time on the TOMASS between the clinical phenotypes. Finally, disease severity showed a significant moderate relation with the severity of dysarthria and a significant weak relation with the severity of dysphagia.

Conclusion

Dysarthria and dysphagia occur in about one-third of patients with MD. It is important for treating physicians to pay attention to this subject because of the influence of both disorders on social participation and wellbeing. Referral to a speech and language therapist should therefore be considered, especially in patients with a more severe clinical phenotype. The swallowing speed, TOMASS and 6MMT are the most clinically relevant tests to administer.

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线粒体疾病患者的构音障碍和吞咽困难
背景有关线粒体疾病(MD)构音障碍和吞咽困难的信息很少。然而,要及早发现言语和吞咽问题、监测病程、制定并提供最佳治疗和支持,就需要这方面的知识。因此,本研究旨在探讨构音障碍和吞咽困难在 MD 患者中的发生率和严重程度及其与临床表型和疾病严重程度的关系。方法这项回顾性横断面病历研究的对象包括 2015 年 1 月至 2023 年 4 月期间在拉德布德线粒体医学中心参加多学科入院治疗、经基因确诊为 MD 的成人(年龄≥ 18 岁)。通过进行拉德布鲁德构音障碍评估、吞咽速度、吞咽困难限制、咀嚼和吞咽固体测试(TOMASS)以及 6 分钟咀嚼测试(6MMT)来检查构音障碍和吞咽困难。研究纳入了 224 名 MD 患者,中位年龄为 42 岁,其中男性占 37.5%。汇总的构音障碍患病率为 33.8%,吞咽困难患病率为 35%。多发性硬化症患者的吞咽速度、TOMASS(总时间)和 6MMT 均与正常值呈负偏离。此外,构音障碍的存在与临床表型之间存在明显的中度关系。不同临床表型的患者在 TOMASS 总时间上有显著的统计学差异。最后,疾病严重程度与构音障碍严重程度呈显著的中度关系,与吞咽困难严重程度呈显著的弱关系。由于这两种障碍会影响患者的社会参与和身心健康,因此主治医生必须重视这一问题。因此,应考虑将患者转介给言语和语言治疗师,尤其是临床表现较为严重的患者。吞咽速度、TOMASS 和 6MMT 是与临床最相关的测试。
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
Molecular genetics and metabolism
Molecular genetics and metabolism 生物-生化与分子生物学
CiteScore
5.90
自引率
7.90%
发文量
621
审稿时长
34 days
期刊介绍: Molecular Genetics and Metabolism contributes to the understanding of the metabolic and molecular basis of disease. This peer reviewed journal publishes articles describing investigations that use the tools of biochemical genetics and molecular genetics for studies of normal and disease states in humans and animal models.
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