由KBTBD13基因变异引起的6型线状性肌病:24例患者的横断面研究

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
Neurology-Genetics Pub Date : 2024-12-05 eCollection Date: 2024-12-01 DOI:10.1212/NXG.0000000000200214
Esmee S B van Kleef, Karlijn Bouman, Joery P F Molenaar, Benno Küsters, Jan T Groothuis, Montse Olivé, Edoardo Malfatti, Erik-Jan Kamsteeg, Baziel G M Van Engelen, Coen A C Ottenheijm, Jonne Doorduin, Nicol C Voermans
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引用次数: 0

摘要

背景和目的:6型线状肌病(NEM6)是荷兰最常见的线状肌病类型。由于尚未获得详细的临床特征,我们在此提供对24例患者的详细评估。方法:在这项横断面研究中,我们对NEM6患者进行了全面的临床评估(病史和神经系统检查)。收集患者的人口统计数据、KBTBD13基因的致病变异、肌酸激酶水平和既往肌肉活检结果。我们评估了与健康相关的生活质量、疲劳严重程度、跌倒发生率、平衡控制(Mini-Balance Evaluation Systems Test [mini - best])、功能性运动评分(motor Function Measure [MFM])和6分钟步行距离。我们使用经颅磁刺激来评估肌肉松弛动力学。结果:共纳入24例患者(女性19例,年龄19-76岁);5名男性[25-57岁])。患者自童年以来报告的主要症状是肌肉无力(n = 23;96%),动作缓慢(n = 23;96%),跑步困难(n = 20;83%)。大多数患者的轴、近端和远端肌肉表现为轻度无力。与对照组相比,与健康相关的生活质量显著降低,疲劳严重程度显著增加。前瞻性100天内,8例患者(33%)至少跌倒1次,其中5例患者(21%)跌倒2次及以上。Mini-BESTest总分中位数为24(21.0-26.0[四分位间距])/ 28,MFM总分中位数为91%(83.5-95.3),均为轻度异常。4例(17%)患者6分钟步行距离低于正常下限。所有NEM6患者的肌肉松弛率均显著降低,中位数为6.5 [4.9-8.1]s-1(正常下限为10.1 s-1)。讨论:这项横断面研究在NEM6患者中显示出相对轻微的临床表型和轻度异常的功能检查。然而,患者报告对日常活动有重要影响,表现为功能困难、生活质量下降、疲劳严重程度增加和跌倒发生率增加。这可能与肌肉松弛延迟有关。本研究提供了NEM6患者的临床表现和功能限制的全面概述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nemaline Myopathy Type 6 Caused by Variants in the KBTBD13 Gene: A Cross-Sectional Study of 24 Patients.

Background and objectives: Nemaline myopathy type 6 (NEM6) is the most prevalent type of nemaline myopathy in the Netherlands. Because a detailed clinical characterization is not available yet, we here provide a detailed assessment of 24 patients.

Methods: In this cross-sectional study, we performed a full clinical assessment (medical history and neurologic examination) in patients with NEM6. Patient demographics, causative variants in the KBTBD13 gene, creatine kinase levels, and the results of previous muscle biopsies were collected. We evaluated experienced health-related quality of life, fatigue severity, prevalence of falls, balance control (Mini-Balance Evaluation Systems Test [Mini-BESTest]), functional motor score (Motor Function Measure [MFM]), and 6-minute walk distance. We used transcranial magnetic stimulation to assess muscle relaxation kinetics.

Results: Twenty-four patients were included (19 women [19-76 years]; 5 men [25-57 years]). Key patient-reported symptoms since childhood were muscle weakness (n = 23; 96%), slowness of movements (n = 23; 96%), and difficulties with running (n = 20; 83%). Axial, proximal, and distal muscles showed mild weakness in most patients. Health-related quality of life was significantly lower, and there was a significantly increased fatigue severity compared with controls. Prospectively, in a period of 100 days, 8 patients (33%) fell at least 1 time, of whom 5 patients (21%) fell 2 times or more. The median total score on the Mini-BESTest was 24 (21.0-26.0 [interquartile range]) of 28 and the median total percentage on the MFM was 91% (83.5-95.3), both considered to be mildly abnormal. The 6-minute walk distance was below the lower limit of normal in 4 patients (17%). All patients with NEM6 showed a markedly reduced muscle relaxation rate with a median of 6.5 [4.9-8.1] s-1 (lower limit of normal is 10.1 s-1).

Discussion: This cross-sectional study in patients with NEM6 shows a relatively mild clinical phenotype and mildly abnormal functional tests. However, patients report an important impact on the daily activities, which is illustrated by functional difficulties, reduced quality of life, increased fatigue severity, and increased prevalence of falls. This might be related to delayed muscle relaxation. This study provides a comprehensive overview of the clinical presentation and functional limitations in patients with NEM6.

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来源期刊
Neurology-Genetics
Neurology-Genetics Medicine-Neurology (clinical)
CiteScore
6.30
自引率
3.20%
发文量
107
审稿时长
15 weeks
期刊介绍: Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. Original articles in all areas of neurogenetics will be published including rare and common genetic variation, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease-genes, and genetic variations with a putative link to diseases. This will include studies reporting on genetic disease risk and pharmacogenomics. In addition, Neurology: Genetics will publish results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials are welcome, including well-powered studies reporting negative results.
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