Acute mitochondrial myopathy with respiratory insufficiency and motor axonal polyneuropathy

作者：Zhou, Ying; Yi, Jianhua; Liu, Li; Wang, Xiaoping; Dong, Liang; Du, Ailian^*

来源：International Journal of Neuroscience, 2018, 128(3): 231-236.

DOI：10.1080/00207454.2017.1387113

• Pure mitochondrial myopathy
• lactic acidosis
• respiratory failure
• acute motor axonal neuropathy
• pyrosequencing

Background: Mitochondrial myopathies (MMs) are mainly presented with chronic muscle weakness and accompanied with other syndromes. MM with acute respiratory insufficiency is rare. Aims: To reveal the clinical, pathological and molecular characteristics of a life-threatening MM. Methods: Muscle biopsy and enzyme staining were performed in skeletal muscles. Mitochondrial DNA (mtDNA) sequencing was analyzed and heteroplasmy were quantified by pyrosequencing. Results: All three patients had tachycardia, acute lactic acidosis, dyspnea and sudden severe muscle weakness. Two patients had calf edema and abdominal pain, and one had a heart attack. Electromyography in two patients showed dramatically decreased axonal amplitudes of motor nerves. Muscle biopsies showed ragged red fibers and dramatic mitochondrial abnormality. A mtDNA m.3243A>G mutation was identified in Patient 1 (mutation load: 29% in blood and 73% in muscle) and Patient 3 (79% in blood and 89% in muscle). A mtDNA m.8344A>G mutation was found in Patient 2 (mutation load 80.4% in blood). Conclusion: MM characterized by lactic acidosis, respiratory failure and acute motor axonal neuropathy is life threatening.

• 出版日期2018
• 单位上海交通大学; 浙江大学