期刊
DIABETES-METABOLISM RESEARCH AND REVIEWS
卷 37, 期 5, 页码 -出版社
WILEY
DOI: 10.1002/dmrr.3381
关键词
diabetes mellitus; type 1; diabetes mellitus; type 2; MODY; monogenic diabetes; sequence analysis; whole-exome sequencing
资金
- National Natural Science Foundation of China [81873634 81400783]
- National Key R&D Program of China [2016YFC1305000 2016YFC1305001 2018YFC1315603]
- Science and Technology Major Project of Hunan Province [2017SK1020]
- Hunan Province Natural Science Foundation of China [2018JJ2573 2020JJ2053]
This study aimed to establish a systematic screening strategy to select candidates for genetic testing among patients with maturity-onset diabetes of the young. A total of 1279 participants were successfully screened using the AACM strategy, with mutations found in a small portion of the cohort. Whole-exome sequencing was used to identify gene mutations.
Aims This study aimed to establish a systematic screening strategy to select candidates for genetic testing among patients with maturity-onset diabetes of the young (MODY) and to accomplish early diagnosis of MODY. Materials and methods We enrolled 1478 sporadic patients from the outpatient department of endocrinology. Out of the1478 patients, 1279 participants were successfully screened according to the AACM strategy, which includes the age of onset, autoantibody to islet antigen, C-peptide and metabolic syndrome. Another six probands and their families who fulfilled the common clinical criteria for MODY were also examined for causative gene mutations. Whole-exome sequencing (WES) was performed to examine the mutations. Results A total of 24 out of 1279 sporadic patients with newly diagnosed diabetes were eligible for genetic testing. Mutations were found in 4/24 participants in the cohort, as well as in 2/6 pedigrees. A likely pathogenic alteration, a likely benign alteration and three alterations with uncertain significance were identified with WES. Most of the mutant genes recognised in our trial were not the most common causative genes of MODY, and all of the mutations were specifically reported in Asian patients only, suggesting a unique genetic background of MODY in different ethnicities. Conclusions In this systematic study of MODY in a new-onset diabetes cohort, MODY cases were incorrectly diagnosed as type 1 diabetes mellitus (T1DM) and type 2 diabetes mellitus (T2DM), suggesting that an observant clinician is necessary for early and correct MODY diagnosis. This systematic approach to screening is practical and specific enough to identify patients who are most appropriate for genetic testing.
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