TY - JOUR
T1 - Association of a Vascular Endothelial Growth Factor genetic variant with Serum VEGF level in subjects with Metabolic Syndrome
AU - Ghazizadeh, Hamideh
AU - Fazilati, Mohammad
AU - Pasdar, Alireza
AU - Avan, Amir
AU - Tayefi, Maryam
AU - Ghasemi, Faeze
AU - Mehramiz, Mehraneh
AU - Mirhafez, Seyed Reza
AU - Ferns, Gordon A.
AU - Azimi-Nezhad, Mohsen
AU - Ghayour-Mobarhan, Majid
PY - 2017/1/20
Y1 - 2017/1/20
N2 - Background The metabolic syndrome (MetS) is a clustering of metabolic disorders that is associated with an increased risk of developing cardiovascular-disease, diabetes, and related diseases. Against this background, Vascular Endothelial Growth Factor (VEGF) plays an essential role in angiogenesis, vascular permeability, and hematopoiesis and its increased level is reported to be associated with increasing the risk of developing cardiovascular-disease, stroke and diabetes. Therefore the aim of present study was to explore the association of serum VEGF level and its associated genetic-polymorphism, rs10738760 (A > G) at 9p24.2, in 850 subjects with/without MetS. Methods MetS was defined according to the International-Diabetes-Federation criteria. Genotyping was carried out using Polymerase chain reaction-amplification refractory mutation system. Anthropometric/biochemical parameters, including FBG, Triglyceride, HDL, TC, etc., were determined followed by univariate and multivariate analyses. Results MetS patients had significantly higher levels of BMI, waist-circumference, cholesterol, triglyceride, Hs-CRP and SBP/DBP, while the HDL-C levels was lower in patients group, compared to control group (P < 0.05). Moreover, our analysis showed that MetS patients with GA or AA genotypes had a significantly (P = 0.03) higher serum level of VEGF. Conclusions we demonstrate an association between a VEGF genetic variant with MetS, suggesting its role as a risk stratification factor for MetS.
AB - Background The metabolic syndrome (MetS) is a clustering of metabolic disorders that is associated with an increased risk of developing cardiovascular-disease, diabetes, and related diseases. Against this background, Vascular Endothelial Growth Factor (VEGF) plays an essential role in angiogenesis, vascular permeability, and hematopoiesis and its increased level is reported to be associated with increasing the risk of developing cardiovascular-disease, stroke and diabetes. Therefore the aim of present study was to explore the association of serum VEGF level and its associated genetic-polymorphism, rs10738760 (A > G) at 9p24.2, in 850 subjects with/without MetS. Methods MetS was defined according to the International-Diabetes-Federation criteria. Genotyping was carried out using Polymerase chain reaction-amplification refractory mutation system. Anthropometric/biochemical parameters, including FBG, Triglyceride, HDL, TC, etc., were determined followed by univariate and multivariate analyses. Results MetS patients had significantly higher levels of BMI, waist-circumference, cholesterol, triglyceride, Hs-CRP and SBP/DBP, while the HDL-C levels was lower in patients group, compared to control group (P < 0.05). Moreover, our analysis showed that MetS patients with GA or AA genotypes had a significantly (P = 0.03) higher serum level of VEGF. Conclusions we demonstrate an association between a VEGF genetic variant with MetS, suggesting its role as a risk stratification factor for MetS.
KW - Metabolic syndrome
KW - PCR
KW - Polymorphism
KW - Serum
KW - VEGF
UR - http://www.scopus.com/inward/record.url?scp=85006268564&partnerID=8YFLogxK
U2 - 10.1016/j.gene.2016.10.034
DO - 10.1016/j.gene.2016.10.034
M3 - Article
C2 - 27984191
AN - SCOPUS:85006268564
VL - 598
SP - 27
EP - 31
JO - Gene
JF - Gene
SN - 0378-1119
ER -