Hinuy Hamilton M, Hirata Mario H, Sampaio Marcelo F, Armaganijan Dikran, Salazar Luis A, Hirata Rosario D C
Department of Clinical and Toxicological Analysis, School of Pharmaceutical Sciences, Sao Paulo University, Sao Paulo, SP, Brazil.
Mol Genet Metab. 2006 Dec;89(4):374-80. doi: 10.1016/j.ymgme.2006.04.012. Epub 2006 Jun 9.
Leptin plays an important role in satiety signaling and is related to obesity. Variants of leptin gene (LEP) have been associated to differences in plasma leptin levels and obesity-related phenotypes. The purpose of this study was to evaluate the association of LEP 3'HVR and leptin concentrations and obesity-related traits in our population. Anthropometrics and systolic/diastolic pressure were measured in 210 unrelated Brazilian individuals. Blood samples were collected for quantification of leptin, glucose and lipids and DNA extraction. LEP 3'HVR polymorphic region was amplified by PCR and fragments were analyzed by polyacrylamide gel electrophoresis. Obesity was associated with hypertension, hyperglycemia, obesity-related traits, plasma leptin and serum lipids (p < 0.05). The frequency of LEP 3'HVR class I alleles (I/I + I/II genotypes) was higher in obese (p = 0.043) than in non-obese individuals. Multivariate logistic regression showed that the risk for obesity is nine times higher in hypertensive individuals and two times higher in class I alleles carriers. The presence of class I alleles was associated with increased BMI and WC. Plasma leptin was related to class I alleles in women (p < 0.05). No association was found between LEP 3'HVR and hypertension or risk factors for CAD in our sample. Our results suggest that LEP 3'HVR is an important predictor for obesity-related traits and leptin plasma levels.
瘦素在饱腹感信号传导中起重要作用,且与肥胖相关。瘦素基因(LEP)的变异与血浆瘦素水平及肥胖相关表型的差异有关。本研究的目的是评估LEP 3'HVR与我们人群中瘦素浓度及肥胖相关特征之间的关联。对210名无亲缘关系的巴西个体进行了人体测量以及收缩压/舒张压测量。采集血样用于瘦素、葡萄糖和脂质的定量分析以及DNA提取。通过聚合酶链反应(PCR)扩增LEP 3'HVR多态性区域,并通过聚丙烯酰胺凝胶电泳分析片段。肥胖与高血压、高血糖、肥胖相关特征、血浆瘦素和血脂相关(p < 0.05)。肥胖个体中LEP 3'HVR I类等位基因(I/I + I/II基因型)的频率高于非肥胖个体(p = 0.043)。多因素逻辑回归显示,高血压个体患肥胖症的风险高9倍,I类等位基因携带者患肥胖症的风险高2倍。I类等位基因的存在与体重指数(BMI)和腰围(WC)增加有关。女性血浆瘦素与I类等位基因有关(p < 0.05)。在我们的样本中,未发现LEP 3'HVR与高血压或冠心病危险因素之间存在关联。我们的结果表明,LEP 3'HVR是肥胖相关特征和血浆瘦素水平的重要预测指标。