Characteristics of maturity onset diabetes of the young in a large diabetes center

被引:52
作者
Chambers, Christina [1 ]
Fouts, Alexandra [1 ]
Dong, Fran [1 ]
Colclough, Kevin [2 ]
Wang, Zhenyuan [3 ]
Batish, Sat Dev [3 ]
Jaremko, Malgorzata [3 ]
Ellard, Sian [2 ]
Hattersley, Andrew T. [2 ]
Klingensmith, Georgeanna [1 ]
Steck, Andrea K. [1 ]
机构
[1] Univ Colorado Denver, Barbara Davis Ctr Childhood Diabet, Mail Stop A140,POB 6511, Aurora, CO 80045 USA
[2] Univ Exeter, Inst Biomed & Clin Sci, Dept Genet, Sch Med, Exeter, Devon, England
[3] Athena Diagnost, Worcester, MA USA
基金
英国惠康基金;
关键词
GCK; HNF1A; HNF4A; MODY; HEPATOCYTE NUCLEAR FACTOR-1-BETA; RANDOM C-PEPTIDE; PHENOTYPIC CHARACTERISTICS; CLINICAL-DIAGNOSIS; GENETIC DIAGNOSIS; GLYCEMIC CONTROL; MUTATIONS; MODY; PREVALENCE; INSULIN;
D O I
10.1111/pedi.12289
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Maturity onset diabetes of the young (MODY) is a monogenic form of diabetes caused by a mutation in a single gene, often not requiring insulin. The aim of this study was to estimate the frequency and clinical characteristics of MODY at the Barbara Davis Center. A total of 97 subjects with diabetes onset before age 25, a random C-peptide 0.1 ng/mL, and negative for all diabetes autoantibodies (GADA, IA-2, ZnT8, and IAA) were enrolled, after excluding 21 subjects with secondary diabetes or refusal to participate. Genetic testing for MODY 1-5 was performed through Athena Diagnostics, and all variants of unknown significance were further analyzed at Exeter, UK. A total of 22 subjects [20 (21%) when excluding two siblings] were found to have a mutation in hepatocyte nuclear factor 4A (n = 4), glucokinase (n = 8), or hepatocyte nuclear factor 1A (n = 10). Of these 22 subjects, 13 had mutations known to be pathogenic and 9 (41%) had novel mutations, predicted to be pathogenic. Only 1 of the 22 subjects had been given the appropriate MODY diagnosis prior to testing. Compared with MODY-negative subjects, the MODY-positive subjects had lower hemoglobin A1c level and no diabetic ketoacidosis at onset; however, these characteristics are not specific for MODY. In summary, this study found a high frequency of MODY mutations with the majority of subjects clinically misdiagnosed. Clinicians should have a high index of suspicion for MODY in youth with antibody-negative diabetes.
引用
收藏
页码:360 / 367
页数:8
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