Key result
LPL rs13702 C allele is linked to ~73% higher type 2 diabetes risk.
Why the study?
The relationship between dyslipidemia and type 2 diabetes mellitus and the role of LPL gene polymorphism in T2DM susceptibility in the Iranian population was evaluated.
Does the rs13702 polymorphism in the LPL gene increase susceptibility to type 2 diabetes in an Iranian population?
Case-Control (n=200)
Does the rs13702 polymorphism in the LPL gene increase susceptibility to type 2 diabetes in an Iranian population?
Odds Ratio: 1.729 (95% CI 1.184–2.523)
p-value: p=0.005
The rs13702 C allele in the LPL gene is associated with an increased susceptibility to Type 2 Diabetes in the Iranian population.
Does not support clinical genetic testing for rs13702; hypothesis-generating for LPL variants in T2D susceptibility.
Background: The relationship between dyslipidemia and type 2 diabetes mellitus (T2DM) has been frequently reported. Lipoprotein lipase (LPL) is considered to be an effective gene in regulating lipid profile. MicroRNAs (miRNAs) are small noncoding RNAs involved in posttranscriptional regulation of gene expression. In the present study, we have evaluated rs13702 (C/T) polymorphism located in miRNA-410 binding site of LPL gene in subset of Iranian T2DM patients and their normal counterparts. Materials and Methods: In this case–control study, 102 T2DM patients and 98 healthy controls were worked out for rs13702 single nucleotide polymorphism genotypes. High resolution meting (HRM) analysis was used for genotyping. Results: C allele of rs13702 C/T polymorphism located in miRNA-410 binding site in LPL gene was detected to be significantly associated with T2DM (C allele; odds ratios (OR) = 1.729 (95% confidential intervals (CI) = 1.184–2.523); P = 0.005) also its CC genotype (OR = 3.28 (95% CI 8.68–1.24); P = 0.010) showed the same association. Conclusion: Correlation of rs13702 C allele with susceptibility to T2DM may be due to the higher level of LPL that leads to increased plasma fatty acids and its entry into peripheral tissues such as skeletal muscle, liver, and adipocytes causing development of insulin resistance and ultimately T2DM.
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Hatefi et al. (2018) conducted a case-control in Type 2 diabetes mellitus (n=200). rs13702 C allele in LPL gene vs. Healthy controls / non-C alleles was evaluated on Type 2 diabetes mellitus (OR 1.729, 95% CI 1.184-2.523, p=0.005). The C allele of the rs13702 polymorphism in the LPL gene was significantly associated with increased susceptibility to type 2 diabetes in an Iranian population (OR 1.729; 95% CI 1.184-2.523; P=0.005).
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