Departamento de Ciencias Básicas, Universidad Católica de la Santísima Concepción, Concepción, Chile.
BHF Glasgow Cardiovascular Research Centre, Institute of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, United Kingdom.
Arch Endocrinol Metab. 2021 Nov 3;65(3):305-314. doi: 10.20945/2359-3997000000359. Epub 2021 Apr 27.
To study the association of gene variants with obesity and metabolic markers in nondiabetic Chilean adults.
This cross-sectional study included 263 non-diabetic adults. The genotype of the rs75493593 polymorphism of SLC16A11 gene was performed by real-time PCR. It's association with adiposity markers (body weight, BMI, waist circumference and fat mass percentage), metabolic markers (glucose, insulin, HOMA, leptin, total cholesterol, LDLc, HDLc, triglycerides, ALT, GGT and hsCRP) and blood pressure was analyzed by linear regression.
The minor allele (T) of the gene (rs75493593) has a frequency of 29.7% among Chileans. Risk genotypes (GT and TT) were associated with a significant 1.49 mU/l increase in plasmatic insulin for each copy of the minor allele (95% CI: 0.12, 2.87, p < 0.05). This association remained significant after adjusting for socio-demographic variables, physical activity and smoking (1.36 mU/l, 95% CI: 0.16, 2.58 p < 0.05), but was lost when BMI was included as a confounding factor. Higher BMI was also significantly associated with polymorphic genotypes in , independent of socio-demographic variables.
The minor allele of the gene (T) is highly prevalent among Chileans and is associated with increased insulin and BMI in nondiabetic individuals. These findings suggest that the genetic variant in is not only associated with type 2 diabetes as previously shown in Mexicans, but is also related to early metabolic alterations in healthy subjects that may lead to type 2 diabetes.
研究智利非糖尿病成年人中基因变异与肥胖和代谢标志物的相关性。
本横断面研究纳入了 263 名非糖尿病成年人。通过实时 PCR 检测 SLC16A11 基因 rs75493593 多态性的基因型。采用线性回归分析其与肥胖标志物(体重、BMI、腰围和体脂百分比)、代谢标志物(血糖、胰岛素、HOMA、瘦素、总胆固醇、LDLc、HDLc、甘油三酯、ALT、GGT 和 hsCRP)和血压的相关性。
该基因(rs75493593)的次要等位基因(T)在智利人中的频率为 29.7%。风险基因型(GT 和 TT)与每增加一个等位基因(95%CI:0.12, 2.87,p<0.05)导致血浆胰岛素显著增加 1.49 mU/l。在调整社会人口统计学变量、体力活动和吸烟因素后,这种相关性仍然显著(1.36 mU/l,95%CI:0.16, 2.58,p<0.05),但当 BMI 作为混杂因素纳入时,这种相关性就消失了。较高的 BMI 也与 基因的多态性基因型显著相关,独立于社会人口统计学变量。
该基因的次要等位基因(T)在智利人中高度流行,与非糖尿病个体中胰岛素和 BMI 的增加有关。这些发现表明,该基因变异不仅与之前在墨西哥人身上显示的 2 型糖尿病相关,而且还与健康受试者中早期代谢改变相关,这可能导致 2 型糖尿病。