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A Screening Approach for Mitochondrial tRNALeu(UUR) A3243G Mutation in a Hospital-Based Population with Diabetes 被引量:4

A Screening Approach for Mitochondrial tRNALeu(UUR) A3243G Mutation in a Hospital-Based Population with Diabetes
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摘要 To the Editor:Diabetes caused by mitochondrial tRNALeu(UUR) A3243G mutation is one of the most common types ofmitochondrial diabetes mellitus (MDM).Seventeen years ago,we reported that the prevalence of MDM was 0.4% in clinically diagnosed type 2 diabetes mellitus (T2DM) patients (n =716).[1] Recently,we reviewed all the studies reporting MDM cases from grade three and first-class hospitals in China (unpublished) and found that the prevalence of MDM in a pooled randomly selected T2DM population was 0.64%.MDM patients are usually characterized by early age at diagnosis,low beta-cell function,and lack of obesity,insulin resistance,and autoantibodies associated with type 1 diabetes mellitus (T1DM). To the Editor:Diabetes caused by mitochondrial tRNALeu(UUR) A3243G mutation is one of the most common types ofmitochondrial diabetes mellitus (MDM).Seventeen years ago,we reported that the prevalence of MDM was 0.4% in clinically diagnosed type 2 diabetes mellitus (T2DM) patients (n =716).[1] Recently,we reviewed all the studies reporting MDM cases from grade three and first-class hospitals in China (unpublished) and found that the prevalence of MDM in a pooled randomly selected T2DM population was 0.64%.MDM patients are usually characterized by early age at diagnosis,low beta-cell function,and lack of obesity,insulin resistance,and autoantibodies associated with type 1 diabetes mellitus (T1DM).
出处 《Chinese Medical Journal》 SCIE CAS CSCD 2018年第9期1117-1119,共3页 中华医学杂志(英文版)
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  • 1I Desehauer M, Mtlller T, Wieser T, et al. Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation. Arch Neurol, 2001,58 : 1885-1888.
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