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Article Abstract

The genetic polymorphism in the nuclear factor erythroid 2-related factor 2 (Nrf2) gene has been reported as one of the prognosis markers for various diseases, including cancer. Nrf2 is a key transcription factor involved in wound healing by regulating angiogenesis. We investigated the genetic association of single-nucleotide polymorphism rs35652124 with T2DM and DFU and assessed its functional impact. A total of 400 subjects were recruited for the study and categorized into three groups: infected DFU patients (DFU, = 100), T2DM patients without complications (T2DM, = 150), and healthy adults with normal glucose tolerance (NGT, = 150). The subjects were genotyped by PCR-RFLP, and the polymorphism was identified by bidirectional Sanger sequencing. The expression of , , , and was studied by qPCR to evaluate the functional impact of rs35652124. The "TT" genotype of rs35652124 was associated with a significant risk for T2DM [OR = 2.2 (1.2-4.2), = 0.01] and DFU [OR = 7.9 (4-14.9), < 0.0001]. A significant decrease in transcriptional levels of and and a remarkable increase in and were observed in subjects with TT genotype. In conclusion, rs35652124 (TT) is a harmful genetic variant that predisposes to insulin resistance and impaired angiogenesis. Hence, it may serve as a diagnostic genetic marker for T2DM and DFU in combination with different inflammatory markers.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7448237PMC
http://dx.doi.org/10.1155/2020/9825028DOI Listing

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