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Lower Circulating miR-122 Level in Patients with HNF1A Variant-Induced Diabetes Compared with Type 2 Diabetes

Authors :
Xiuting Huang
Siqian Gong
Yumin Ma
Xiaoling Cai
Lingli Zhou
Yingying Luo
Meng Li
Wei Liu
Simin Zhang
Xiuying Zhang
Qian Ren
Yu Zhu
Xianghai Zhou
Rui Zhang
Ling Chen
Xueying Gao
Fang Zhang
Yanai Wang
Xueyao Han
Linong Ji
Source :
Journal of Diabetes Research, Vol 2018 (2018)
Publication Year :
2018
Publisher :
Wiley, 2018.

Abstract

miR-122, the expression of which is regulated by several transcription factors, such as HNF1A, was recently reported to be associated with type 2 diabetes (T2DM) and hepatocellular carcinoma. HNF1A variants can cause diabetes and might be involved in the development of primary liver neoplasm. Differences in miR-122 expression among different types of diabetes have not been studied. This study aimed to investigate differences in serum miR-122 levels in Chinese patients with different forms of diabetes, including T2DM, type 1 diabetes (T1DM), HNF1A variant-induced diabetes (HNF1A-DM), glucokinase variant-induced diabetes (GCK-DM), and mitochondrial A3243G mutation-induced diabetes (MDM). In total, 12 HNF1A-DM patients, 24 gender-, age-, and body mass index-matched (1 : 2) T2DM patients and 24 healthy subjects were included in this study. In addition, 30 monogenic diabetes (11 GCK-DM and 19 MDM) and 17 T1DM patients were included. Fasted blood biochemistry and miR-122 were measured. The results showed that the HNF1A-DM patients had lower miR-122 levels [0.046 (0.023, 0.121)] than T2DM patients [0.165 (0.036, 0.939), P=0.02] and healthy controls [0.249 (0.049, 1.234), P=0.019]. The area under the curve of the receiver operating characteristic curve for miR-122 to discriminate HNF1A-DM and T2DM was 0.687 (95% CI: 0.52–0.86, P=0.07). There was no difference in serum miR-122 among HNF1A-DM, GCK-DM, MDM, and T1DM patients. Lower serum miR-122 is a unique feature of HNF1A-DM patients and might partially explain the increased risk for liver neoplasm and abnormal lipid metabolism in HNF1A-DM patients.

Details

Language :
English
ISSN :
23146745 and 23146753
Volume :
2018
Database :
Directory of Open Access Journals
Journal :
Journal of Diabetes Research
Publication Type :
Academic Journal
Accession number :
edsdoj.ff9fff40edf643fa8971d42be15bf5d0
Document Type :
article
Full Text :
https://doi.org/10.1155/2018/7842064