The (FTO) gene polymorphism is associated with metabolic syndrome risk in Egyptian females: a case-control study

被引:41
作者
Khella, Mina S. [1 ]
Hamdy, Nadia M. [1 ]
Amin, Ashraf I. [2 ]
El-Mesallamy, Hala O. [1 ]
机构
[1] Ain Shams Univ, Fac Pharm, Biochem Dept, African Union Org St, Cairo 11566, Egypt
[2] NIDE, Clin Pathol & Lab Dept, Cairo, Egypt
关键词
FTO; Obesity; SNP; T2DM; Alt; HDL c; Metabolic syndrome; Serum lipids; OBESITY-ASSOCIATED GENE; FAT MASS; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; VARIANT RS9939609; ENERGY-INTAKE; BODY-MASS; RANGE; ADOLESCENTS; STATEMENT;
D O I
10.1186/s12881-017-0461-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: Variations within fat mass and obesity associated (FTO) gene had crosstalk with obesity risk in European and some Asian populations. This study was designed to investigate FTO rs9939609 association with metabolic syndrome (MetS) as well as biochemical parameters as plasma glucose, serum triacylglycerol (TAG), total cholesterol (TC) and transaminases enzymes in Arab female population from Egypt. Methods: In order to achieve that, FTO gene rs9939609 (A < T) was genotyped using TaqMan SNP Genotyping Assay in a total of 197 females which were enrolled in this study. Fasting levels of serum insulin, lipid profile and plasma glucose, in addition to liver transaminases were measured. The association between the genotype distribution and MetS risk was evaluated using Chi-square and logistic regression tests in a case-control design under different genetic models. Results: The association of genotype distribution with MetS was significant (x(2) = 8.6/P = 0.014) with an increased odds ratio under dominant model (OR = 1.97, P = 0.029 and 95% C.I = 1.07-3.6) and recessive model (OR = 2.95, P = 0.017 and 95%C.I = 1.22-7.22). Moreover, (AA) subjects showed significant lower HDL-C levels (P = 0.009) when compared to (TT) ones. In addition, interestingly subjects with (AA) genotype have significantly higher ALT levels (P = 0.02) that remained significant after correction of major confounders as body mass index and serum triacylglycerols but not after conservative Bonferroni adjustment. Conclusions: The present study shows for first time that FTO gene rs9939609 is genetic risk factor for metabolic syndrome in Egyptian population which may help in understanding the biology of this complex syndrome and highlighted that this association may be through HDL-C component. The association of this genetic polymorphism with ALT levels needs to be studied in other populations with larger sample size.
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