Exacerbation of myopathy triggered by antiobesity drugs in a patient with multiple acyl-CoA dehydrogenase deficiency

被引:5
作者
Lin, Po-Yu [1 ]
Liang, Wen-Chen [2 ,3 ]
Liao, Wei-An [4 ]
Sun, Yuan-Ting [1 ,5 ]
机构
[1] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Neurol, Tainan, Taiwan
[2] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Dept Pediat, Kaohsiung, Taiwan
[3] Kaohsiung Med Univ, Coll Med, Sch Med, Dept Pediat, Kaohsiung, Taiwan
[4] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Coll Med, Dept Pathol, Tainan, Taiwan
[5] Natl Cheng Kung Univ, Natl Cheng Kung Univ Hosp, Dept Genom Med, Coll Med, Tainan, Taiwan
关键词
Metformin; Multiple acyl-coA dehydrogenase deficiency; Thyroid hormones; Topiramate;
D O I
10.1186/s12883-021-02121-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundMultiple acyl-CoA dehydrogenase deficiency (MADD) is a treatable lipid metabolism disorder that presents as myopathy and episodic metabolic crisis. The metabolic crisis is typically associated with prolonged fasting or physical stress; however, the mechanism of metabolic crisis is not yet fully understood.Case presentationA 28-year-old Taiwanese woman presented with dyspnoea, poor appetite, and muscle weakness after using antiobesity drugs, including metformin, triiodothyronine, and topiramate. MADD was diagnosed, and her symptoms rapidly improved after treatment with riboflavin, carnitine, and ubiquinone. To date, antiobesity drugs have not been reported to be a provoking factor in fatty acid oxidation disorder.ConclusionsThe increase of beta -oxidation activity due to antiobesity drugs supports the hypothetical substrate competition model for MADD metabolic crisis. Because the drugs our patient used are commonly prescribed, we report this case to increase the vigilance and proactivity of clinicians in recognising this treatable adult-onset myopathy.
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页数:5
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