TY - JOUR
T1 - Association of vascular endothelial growth factor gene +405 C>G and -460 C>T polymorphism with diabetic foot ulcer in Indonesia
AU - Dahlan, Kemas Muhammad
AU - Pratama, Dedy
AU - Muradi, Akhmadu
AU - Anita Suryandari, Dwi
AU - Yunaini, Luluk
AU - Boediningsih, Setyawati
N1 - Publisher Copyright:
© 2019 Published under licence by IOP Publishing Ltd.
PY - 2019/7/15
Y1 - 2019/7/15
N2 - Background, the greatest risk factor for Diabetic foot ulcer (DFU) is neuropathy. Vascular endothelial growth factor (VEGF) gene is a gene encodes a protein vascular endothelial growth factor (VEGF), which has a function of angiogenesis and neurogenesis. VEGF plays a role in neuropathy, angiopathy and wound healing in DFU. Methods: Case-control study, case is types 2 DM with DFU and control is type 2 DM without DFU, Polymerase Chain Reaction-Restriction Fragment length polymorphism was done to find genotype polymorphism of VEGF gene. Results: Genotype GG VEGF + 405C> G does not have a significant association with DFU in DM patients (GG + CG / CC; OR; 0.52, 95% CI; 0.15 to 1.73 p; 0.289). G allele is proposed as a protective factor in DFU (OR; 0.86, 95% CI 0.57 to 1.28, and p; 0.456). Genotype TT from VEGF gene -460 C> T; have no significant association with DFU (TT + CT / CC; OR; 0.97, 95% CI; 0.41 to 2.26 and p; 0.942). T allele is predicted as protective factor in DFU (OR; 0.90, 95% CI; 0.59 to 1.37 and p; 0,641). Conclusion: G alleles and T alleles are predicted as a protective factor in DM patients associated with DFU.
AB - Background, the greatest risk factor for Diabetic foot ulcer (DFU) is neuropathy. Vascular endothelial growth factor (VEGF) gene is a gene encodes a protein vascular endothelial growth factor (VEGF), which has a function of angiogenesis and neurogenesis. VEGF plays a role in neuropathy, angiopathy and wound healing in DFU. Methods: Case-control study, case is types 2 DM with DFU and control is type 2 DM without DFU, Polymerase Chain Reaction-Restriction Fragment length polymorphism was done to find genotype polymorphism of VEGF gene. Results: Genotype GG VEGF + 405C> G does not have a significant association with DFU in DM patients (GG + CG / CC; OR; 0.52, 95% CI; 0.15 to 1.73 p; 0.289). G allele is proposed as a protective factor in DFU (OR; 0.86, 95% CI 0.57 to 1.28, and p; 0.456). Genotype TT from VEGF gene -460 C> T; have no significant association with DFU (TT + CT / CC; OR; 0.97, 95% CI; 0.41 to 2.26 and p; 0.942). T allele is predicted as protective factor in DFU (OR; 0.90, 95% CI; 0.59 to 1.37 and p; 0,641). Conclusion: G alleles and T alleles are predicted as a protective factor in DM patients associated with DFU.
UR - http://www.scopus.com/inward/record.url?scp=85069997098&partnerID=8YFLogxK
U2 - 10.1088/1742-6596/1246/1/012008
DO - 10.1088/1742-6596/1246/1/012008
M3 - Conference article
AN - SCOPUS:85069997098
SN - 1742-6588
VL - 1246
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
IS - 1
M1 - 012008
T2 - 1st Sriwijaya International Conference on Medical Sciences, SICMS 2018
Y2 - 26 October 2018 through 27 October 2018
ER -