Structural changes and contractility in muscle assessed by magnetic resonance imaging in individuals with ryanodine receptor 1-related rhabdomyolysis or myalgia.

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Muscle & Nerve Pub Date : 2024-10-01 Epub Date: 2024-07-24 DOI:10.1002/mus.28219
Zhe Lyu, Tuva Åsatun Solheim, Nanna Scharff Poulsen, Anne-Sofie Vibæk Eisum, Gry Hatting Beha, Freja Fornander, Annarita Ghosh Andersen, Nanna Witting, John Vissing
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Abstract

Introduction/aims: Ryanodine receptor 1 (RYR1)-related myopathies associated with variants in the RYR1 gene present with a wide range of symptoms and severity. Two of the milder phenotypes associated with dominant pathogenic variants in RYR1 are rhabdomyolysis and myalgia. Only a few studies have investigated the muscle function and structure of individuals with RYR1-related rhabdomyolysis/myalgia objectively, showing inconsistent results. This study aimed to describe structural changes and contractility of muscles in individuals with RYR1-related rhabdomyolysis/myalgia.

Methods: We investigated 15 individuals with dominant variants in the RYR1-gene and compared them with 15 age-, sex-, and body mass index (BMI)-matched controls using MRI, stationary isokinetic dynamometry, and comprehensive clinical evaluation.

Results: No significant differences were found between individuals with RYR1-related rhabdomyolysis/myalgia and healthy controls in peak torque, fat fraction, cross-sectional area, contractile cross-sectional area, or contractility (p > .05) in muscles of the lower back (MRI data only), thigh, or calf. On clinical examination, three individuals exhibited weakness in hip or back extension on the Medical Research Council (MRC) test and eight had muscle hypertrophy. Individuals with weakness were not hypertrophic.

Discussion: Most individuals with RYR1-related rhabdomyolysis/myalgia have close to normal strength, and normal fat fraction and contractility of muscles, and therefore constitute a mild phenotype of RYR1-related myopathies.

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通过磁共振成像评估雷诺丁受体 1 相关横纹肌溶解症或肌痛患者肌肉的结构变化和收缩能力。
导言/目的:与 RYR1 基因变异相关的 Ryanodine 受体 1(RYR1)肌病的症状和严重程度各不相同。与 RYR1 显性致病变异相关的两种较轻的表型是横纹肌溶解症和肌痛。只有少数研究对 RYR1 相关横纹肌溶解症/肌痛患者的肌肉功能和结构进行了客观调查,结果并不一致。本研究旨在描述 RYR1 相关横纹肌溶解症/肌痛患者的肌肉结构变化和收缩能力:我们对 15 名 RYR1 基因显性变异患者进行了调查,并通过核磁共振成像、静态等速肌力测定法和综合临床评估,将他们与 15 名年龄、性别和体重指数(BMI)相匹配的对照者进行了比较:结果:RYR1 相关横纹肌溶解症/肌痛患者与健康对照组患者在下背部肌肉(仅核磁共振成像数据)、大腿肌肉或小腿肌肉的峰值扭矩、脂肪率、横截面积、收缩横截面积或收缩力(P > .05)方面均无明显差异。在临床检查中,3 人在医学研究委员会(MRC)测试中表现出臀部或背部伸展无力,8 人肌肉肥大。患有肌肉无力的患者并不肥大:讨论:大多数 RYR1 相关横纹肌溶解症/肌痛患者的力量接近正常,肌肉的脂肪率和收缩力也正常,因此属于 RYR1 相关肌病的轻度表型。
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来源期刊
Muscle & Nerve
Muscle & Nerve 医学-临床神经学
CiteScore
6.40
自引率
5.90%
发文量
287
审稿时长
3-6 weeks
期刊介绍: Muscle & Nerve is an international and interdisciplinary publication of original contributions, in both health and disease, concerning studies of the muscle, the neuromuscular junction, the peripheral motor, sensory and autonomic neurons, and the central nervous system where the behavior of the peripheral nervous system is clarified. Appearing monthly, Muscle & Nerve publishes clinical studies and clinically relevant research reports in the fields of anatomy, biochemistry, cell biology, electrophysiology and electrodiagnosis, epidemiology, genetics, immunology, pathology, pharmacology, physiology, toxicology, and virology. The Journal welcomes articles and reports on basic clinical electrophysiology and electrodiagnosis. We expedite some papers dealing with timely topics to keep up with the fast-moving pace of science, based on the referees'' recommendation.
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