Sirbu Anca Elena, Buburuzan Laura, Kevorkian Steliana, Martin Sorina, Barbu Carmen, Copaescu Catalin, Smeu Bogdan, Fica Simona
"Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania; Elias University Hospital, bd Marasti, 17, sector 1, Bucharest.
Endokrynol Pol. 2018;69(3):252-258. doi: 10.5603/EP.a2018.0026. Epub 2018 Apr 12.
Visceral adiposity is associated with decreased serum adiponectin levels, peripheral resistance to insulin and an increased risk of cardio-metabolic complications. However, the link between adiponectin expression in visceral adipose tissue (VAT), its serum levels and metabolic protection is controversial. The aim of this study was to investigate the relationship between the adiponectin gene expression in VAT and clinical and metabolic parameters in patients with severe obesity.
This is a cross-sectional study that included 51 severely obese patients (age 43.24±11.29 years, BMI 45.13±8.67 kg/m2), extensively evaluated clinically and biologically (metabolic tests, serum adiponectin measurements, HOMA-IR) before bariatric surgery. Omental adipose tissue was sampled during the intervention and the relative quantification of adiponectin gene expression was performed by real-time PCR, using beta-actin as reference gene.
Adiponectin mRNA in VAT was significantly higher in obese insulin-sensitive patients than in the rest of obese patients (p < 0.05) and negatively correlated with HOMA-IR (r =-0.354, p=0.016) and uric acid (r =-0.304, p=0.045). After adjustment for gender, TG/HDL ratio and uric acid, adiponectin expresion (β= -0.439, p=0.001), waist circumference (β=0.467, p=0.001) and serum adiponectin (β =-0.339, p=0.011) remained significantly associated with HOMA-IR, together explaining more than 50% of its variation.
In severely obese patients, adiponectin gene expression in VAT is negatively correlated with serum levels of uric acid and is an independent determinant, together with anthropometric parameters of visceral obesity and serum adiponectin levels, of insulin resistance.
内脏脂肪过多与血清脂联素水平降低、外周胰岛素抵抗以及心血管代谢并发症风险增加有关。然而,内脏脂肪组织(VAT)中脂联素表达、其血清水平与代谢保护之间的联系存在争议。本研究旨在探讨严重肥胖患者VAT中脂联素基因表达与临床及代谢参数之间的关系。
这是一项横断面研究,纳入了51例严重肥胖患者(年龄43.24±11.29岁,BMI 45.13±8.67 kg/m²),在进行减肥手术前对其进行了全面的临床和生物学评估(代谢测试、血清脂联素测量、HOMA-IR)。在干预过程中采集网膜脂肪组织样本,并以β-肌动蛋白作为参照基因,通过实时PCR对脂联素基因表达进行相对定量。
肥胖且胰岛素敏感患者的VAT中脂联素mRNA显著高于其他肥胖患者(p < 0.05),且与HOMA-IR(r = -0.354,p = 0.016)和尿酸(r = -0.3;04,p = 0.045)呈负相关。在对性别、TG/HDL比值和尿酸进行校正后,脂联素表达(β = -0.439,p = 0.001)、腰围(β = 0.467,p = 0.001)和血清脂联素(β = -0.339,p = 0.011)仍与HOMA-IR显著相关,共同解释了其超过50%的变异。
在严重肥胖患者中,VAT中脂联素基因表达与尿酸血清水平呈负相关,并且与内脏肥胖的人体测量参数和血清脂联素水平一起,是胰岛素抵抗的独立决定因素。