scholarly journals Relationship of microRNA locus with type 2 diabetes mellitus: a case-control study

2021 ◽  
Author(s):  
Qiuyu Huang ◽  
Hanshen Chen ◽  
Fan Xu ◽  
Chao Liu ◽  
Yafeng Wang ◽  
...  

Type 2 diabetes mellitus (T2DM) is considered as a metabolic disease with hyperglycemia. Accumulating investigations have explored the important role of hereditary factors for T2DM occurrence. Some functional microRNA (miR) polymorphisms may affect their interactions with target mRNAs and result in an aberrant expression. Thus, miR-variants might be considered as a biomarker of the susceptibility of T2DM. In this study, we recruited 502 T2DM cases and 782 healthy subjects. We selected miR-146a rs2910164 C>G, -196a2 rs11614913 T>C and -499 rs3746444 A>G loci and carried out an investigation to identify whether these miR- loci could influence T2DM occurrence. In this investigation, a Bonferroni correction was harnessed. After adjustment, we found that rs2910164 single nucleotide polymorphism (SNP) was a protective factor for T2DM (GG vs. CC/CG: adjusted P=0.010), especially in never drinking (GG vs. CC/CG: adjusted P=0.001) and ≥24 kg/m2 (GG vs. CC/CG: adjusted P=0.002) subgroups. We also identified that rs11614913 SNP was a protective factor for T2DM in smoking subjects (CC/TC vs. TT: adjusted P=0.002). When we analyzed an interaction of SNP-SNP with the susceptibility of T2DM. Rs11614913/rs3746444, Rs2910164/rs3746444, and rs11614913/rs2910164 combinations were not associated with the risk of T2DM. In summary, the present study highlights that rs2910164 SNP decreases a susceptibility of T2DM, especially in BMI ≥24 kg/m2 and never drinking subgroups. In addition, we also identify that rs11614913 C allele decreases the susceptibility of T2DM significantly in smoking subgroup.

2016 ◽  
Vol 02 ◽  
pp. 118
Author(s):  
M Vignesh ◽  
T Sangeetha ◽  
T Varsha ◽  
◽  
◽  
...  

Type 2 diabetes mellitus (T2DM) is one of the threatening disorders in the world. It affects people of all ages. Type 2 diabetes mellitus is a condition in which the glucose level in the blood is elevated due to improper function of the secretion of insulin from beta cells of the pancreas. It is a multifactorial disease because it is caused by both environmental and hereditary factors. One of the genes which play an important role in type 2 diabetes mellitus is SLC30A8 which encodes for zinc transporter ZnT8. The common polymorphic site for SLC30A8 is rs13266634. This single-nucleotide polymorphism leads to type 2 diabetes mellitus by replacing the arginine residue with tryptophan residue. This review mainly focuses on the polymorphic studies in the gene SLC30A8 and its association with type 2 diabetes mellitus.


Author(s):  
Nermien Abd El Rahman Ibraheim ◽  
Fatema El Zahraa Sayed Bukhary ◽  
Yehia Zakareia Mahmoud ◽  
Mahmoud Ragab Mohamed ◽  
Salama Rabei Abdel-Rahim

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