Endocrinology and Nutrition Research Center, School of Medicine, Department of Endocrinology and Nutrition, Hospital Clinico Universitario, University of Valladolid, 47130 Valladolid, Spain.
Nutrients. 2023 Dec 7;15(24):5028. doi: 10.3390/nu15245028.
: The present study was designed to investigate SNP rs17300539 in the gene and its relationships with obesity, metabolic syndrome (MS), and serum circulating adiponectin. : The present design involved a Caucasian population of 329 subjects with obesity. Anthropometric and adiposity parameters, blood pressure, biochemical parameters, and the percentage of patients with metabolic syndrome were recorded. The gene variant (rs17300539) genotype was evaluated. : The percentage of patients with different genotypes of the rs17300539 polymorphism in this sample was 86.0% (n = 283) (GG), 11.2% (n = 37) (GA), and 2.7% (n = 9) (AA). The allele frequency was G (0.76) and A (0.24). Applying the dominant genetic model (GG vs. GA AA), we reported differences between genotype GG and genotype GA AA for serum adiponectin levels (Delta: 7.5 ± 1.4 ng/mL; = 0.03), triglycerides (Delta: 41.1 ± 3.4 mg/dL; = 0.01), fastingcirculating insulin (Delta: 4.9 ± 1.1 mUI/L; = 0.02), and insulin resistance as HOMA-IR (Delta: 1.4 ± 0.1 units; = 0.02). The remaining biochemical parameters were not related to the genotype of obese patients. The percentages of individuals with MS (OR = 2.07, 95% CI = 1.3-3.88; = 0.01), hypertriglyceridaemia (OR = 2.66, 95% CI = 1.43-5.01; = 0.01), and hyperglycaemia (OR = 3.31, 95% CI = 1.26-8.69; = 0.02) were higher in GG subjects than patients with A allele. Logistic regression analysis reported an important risk of the presence of metabolic syndrome in GG subjects (OR = 1.99, 95% CI = 1.21-4.11; = 0.02) after adjusting for adiponectin, dietary energy intakes, gender, weight, and age. : The GG genotype of rs17300539 is associated with hypertriglyceridaemia, insulin resistance, low adiponectin levels, and a high risk of metabolic syndrome and its components.
本研究旨在探讨基因中的 SNP rs17300539 及其与肥胖、代谢综合征(MS)和血清循环脂联素的关系。
本设计涉及一个由 329 名肥胖患者组成的白种人群体。记录了人体测量和肥胖参数、血压、生化参数以及代谢综合征患者的百分比。评估了基因变异(rs17300539)的基因型。
在该样本中,rs17300539 多态性的不同基因型患者的百分比为 86.0%(n=283)(GG)、11.2%(n=37)(GA)和 2.7%(n=9)(AA)。等位基因频率为 G(0.76)和 A(0.24)。应用显性遗传模型(GG 与 GA AA),我们报告了基因型 GG 与 GA AA 之间血清脂联素水平的差异(Delta:7.5±1.4ng/ml;=0.03)、甘油三酯(Delta:41.1±3.4mg/dl;=0.01)、空腹循环胰岛素(Delta:4.9±1.1mUI/L;=0.02)和胰岛素抵抗作为 HOMA-IR(Delta:1.4±0.1 单位;=0.02)。其余生化参数与肥胖患者的基因型无关。MS(OR=2.07,95%CI=1.3-3.88;=0.01)、高甘油三酯血症(OR=2.66,95%CI=1.43-5.01;=0.01)和高血糖(OR=3.31,95%CI=1.26-8.69;=0.02)的个体百分比在 GG 受试者中更高。Logistic 回归分析报告了在调整脂联素、膳食能量摄入、性别、体重和年龄后,GG 受试者代谢综合征存在的重要风险(OR=1.99,95%CI=1.21-4.11;=0.02)。
rs17300539 的 GG 基因型与高甘油三酯血症、胰岛素抵抗、低脂联素水平以及代谢综合征及其成分的高风险相关。