生化和化学肌病是竞技游泳运动员线粒体疾病的孤立初始表现。

Josef Finsterer
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引用次数: 0

摘要

孤立且无症状的肌酸激酶升高(高ckemia)可能是线粒体疾病(MID)的初始表现之一。我们报告了一位无症状的患者,意外发现孤立的高ck血症和呼吸链功能障碍分别作为化学和生化MID的指标。一名23岁男子参加竞技运动(游泳),因意外发现无症状和孤立的高肾血症而接受检查。临床神经学检查正常,但血液检查显示肌酸激酶(CK)、天冬氨酸转氨酶、丙氨酸转氨酶、乳酸脱氢酶和醛缩酶升高。乳酸压力测试在自行车计力器上是正常的。针刺肌电图没有提供信息,但肌肉活检提示MID,生化检查显示复合复合物ii, -III和-IV缺陷。在接下来的15年里,高ckemia无症状地持续存在,他继续进行体育活动。综上所述,无症状高肾血症伴多重呼吸链复杂性缺陷可能是MID多年的唯一表现。无症状的化学或生化mid可从持续的体育活动中获益。对孤立的持续性高肾血症的检查可以在单个病例中揭示亚临床线粒体病理。
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Biochemical and Chemical Myopathy as Isolated Initial Manifestation of a Mitochondrial Disorder in a Competitive Swimmer.

Abstract: Isolated and asymptomatic elevation of creatine kinase (hyper-CKemia) can be one of the initial manifestations of a mitochondrial disorder (MID). We present an asymptomatic patient with accidently detected isolated hyper-CKemia and respiratory chain dysfunction as indicators of a chemical and biochemical MID, respectively. A 23-year-old man who performed competitive sport (swimming) underwent workup for accidentally detected asymptomatic and isolated hyper-CKemia. Clinical neurologic examination was normal, but blood tests revealed elevation of creatine kinase (CK), aspartate aminotransferase, alanine aminotransferase, lactate dehydrogenase, and aldolase. Lactate stress testing on a bicycle ergometer was normal. Needle electromyography was noninformative, but muscle biopsy was indicative of a MID, and biochemical investigations revealed a combined complex-II, -III, and -IV defect. Hyper-CKemia persisted asymptomatically over the next 15 years, and he continued with his sports activities. In conclusion, asymptomatic hyper-CKemia together with multiple respiratory chain complex deficiencies can be the only manifestations of a MID over years. Asymptomatic chemical or biochemical MIDs may profit from continuous physical activity. Workup for isolated persisting hyper-CKemia may reveal subclinical mitochondrial pathology in single cases.

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来源期刊
CiteScore
1.60
自引率
0.00%
发文量
64
期刊介绍: Journal of Clinical Neuromuscular Disease provides original articles of interest to physicians who treat patients with neuromuscular diseases, including disorders of the motor neuron, peripheral nerves, neuromuscular junction, muscle, and autonomic nervous system. Each issue highlights the most advanced and successful approaches to diagnosis, functional assessment, surgical intervention, pharmacologic treatment, rehabilitation, and more.
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