Department of Neurology, Radboud University Medical Centre, Nijmegen,Netherlands.
Malignant Hyperthermia Investigation Unit, Canisius Wilhelmina Hospital, Nijmegen,Netherlands.
Curr Pharm Des. 2022;28(1):2-14. doi: 10.2174/1381612827666210804095300.
Variants in the ryanodine receptor-1 gene (RYR1) have been associated with a wide range of neuromuscular conditions, including various congenital myopathies and malignant hyperthermia (MH). More recently, a number of RYR1 variants, mostly MH-associated, have been demonstrated to contribute to rhabdomyolysis events not directly related to anesthesia in otherwise healthy individuals. This review focuses on RYR1-related rhabdomyolysis in the context of several clinical presentations (i.e., exertional rhabdomyolysis, exertional heat illnesses and MH), and conditions involving a similar hypermetabolic state, in which RYR1 variants may be present (i.e., neuroleptic malignant syndrome and serotonin syndrome). The variety of triggers that can evoke rhabdomyolysis, on their own or in combination, as well as the number of potentially associated complications, illustrates that this is a condition relevant to several medical disciplines. External triggers include but are not limited to strenuous physical exercise, especially if unaccustomed or performed under challenging environmental conditions (e.g., high ambient temperature or humidity), alcohol/illicit drugs, prescription medication (in particular statins, other anti-lipid agents, antipsychotics and antidepressants) infection, or heat. Amongst all patients presenting with rhabdomyolysis, genetic susceptibility is present in a proportion, with RYR1 being one of the most common genetic causes. Clinical clues for a genetic susceptibility include recurrent rhabdomyolysis, creatine kinase (CK) levels above 50 times the upper limit of normal, hyperCKemia lasting for 8 weeks or longer, drug/medication doses insufficient to explain the rhabdomyolysis event, and positive family history. For the treatment or prevention of RYR1-related rhabdomyolysis, the RYR1 antagonist dantrolene can be administered, both in the acute phase or prophylactically in patients with a history of muscle cramps and/or recurrent rhabdomyolysis events. Aside from dantrolene, several other drugs are being investigated for their potential therapeutic use in RYR1-related disorders. These findings offer further therapeutic perspectives for humans, suggesting an important area for future research.
RYR1 基因变异与广泛的神经肌肉疾病有关,包括各种先天性肌病和恶性高热(MH)。最近,许多 RYR1 变异体,主要与 MH 相关,已被证明会导致与麻醉无关的横纹肌溶解事件,而这些个体在其他方面是健康的。本综述重点介绍了 RYR1 相关的横纹肌溶解症在几种临床表现(即运动性横纹肌溶解症、运动性热病和 MH)和涉及类似高代谢状态的情况下的情况,在这些情况下可能存在 RYR1 变异体(即神经阻滞剂恶性综合征和血清素综合征)。可以单独或组合引发横纹肌溶解症的各种触发因素,以及与之相关的潜在并发症数量,说明了这是一种与多个医学学科相关的疾病。外部触发因素包括但不限于剧烈的体力活动,尤其是不习惯或在具有挑战性的环境条件下进行的活动(例如,高环境温度或湿度)、酒精/非法药物、处方药物(特别是他汀类药物、其他抗脂质药物、抗精神病药和抗抑郁药)、感染或高温。在所有出现横纹肌溶解症的患者中,遗传易感性存在一定比例,其中 RYR1 是最常见的遗传原因之一。遗传易感性的临床线索包括反复发生的横纹肌溶解症、肌酸激酶(CK)水平高于正常上限的 50 倍、CK 升高持续 8 周或更长时间、药物/药物剂量不足以解释横纹肌溶解症事件以及阳性家族史。对于 RYR1 相关的横纹肌溶解症的治疗或预防,可以使用 RYR1 拮抗剂丹曲林钠,无论是在急性阶段还是在有肌肉痉挛和/或反复横纹肌溶解症史的患者中预防性使用。除了丹曲林钠外,还在研究几种其他药物在 RYR1 相关疾病中的潜在治疗用途。这些发现为人类提供了进一步的治疗前景,表明这是未来研究的一个重要领域。