Lee Ji-Won, Im Jee-Aee, Lee Hye-Ree, Shim Jae-Yong, Youn Byung-S, Lee Duk-Chul
Department of Family Medicine, Yonsei University, College of Medicine, Yong-dong Severance Hospital, Kangnam P.O. Box 1217, Seoul, Korea.
Obesity (Silver Spring). 2007 Sep;15(9):2225-32. doi: 10.1038/oby.2007.264.
Retinol binding protein-4 (RBP4) has been reported to impair insulin sensitivity throughout the body. We investigated the relationship between serum RBP4 levels and adiposity indices as well as metabolic risk variables.
We recruited a total of 102 healthy women 21 to 67 years old. We assessed body composition by computed tomography and divided the study population into four groups based on body weight and visceral fat area (non-obese without visceral adiposity, non-obese with visceral adiposity, obese without visceral adiposity, and obese with visceral adiposity). Serum RBP4 levels were measured by radioimmunoassay.
Despite similar levels of total body fat, non-obese women had lower systolic blood pressure, total cholesterol, triglyceride (TG), low-density lipoprotein (LDL)-cholesterol levels, insulin resistance indices, and RBP4 levels than non-obese women with visceral adiposity and had higher high-density lipoprotein-cholesterol levels. Similarly, obese women without visceral adiposity had lower blood pressure, total cholesterol, TG levels, insulin resistance indices, and RBP4 levels than obese women with visceral adiposity. In addition, despite having increased body fat, obese women without visceral adiposity had lower TGs, insulin resistance indices, and serum RBP4 levels than non-obese women with visceral adiposity. By step-wise multiple regression analysis, visceral fat areas and LDL-cholesterol levels independently affected RBP4 levels.
We determined that serum RBP4 levels are independently associated with visceral fat and LDL-cholesterol levels. These results suggest that, irrespective of body weight, visceral obesity is an independent predictor of serum RBP4 levels, and RBP4 may represent a link between visceral obesity and cardiovascular disease.
据报道,视黄醇结合蛋白4(RBP4)会损害全身的胰岛素敏感性。我们研究了血清RBP4水平与肥胖指数以及代谢风险变量之间的关系。
我们共招募了102名年龄在21至67岁之间的健康女性。通过计算机断层扫描评估身体成分,并根据体重和内脏脂肪面积将研究人群分为四组(无内脏肥胖的非肥胖者、有内脏肥胖的非肥胖者、无内脏肥胖的肥胖者和有内脏肥胖的肥胖者)。通过放射免疫测定法测量血清RBP4水平。
尽管总体脂肪水平相似,但无内脏肥胖的非肥胖女性的收缩压、总胆固醇、甘油三酯(TG)、低密度脂蛋白(LDL)胆固醇水平、胰岛素抵抗指数和RBP4水平均低于有内脏肥胖的非肥胖女性,且高密度脂蛋白胆固醇水平更高。同样,无内脏肥胖的肥胖女性的血压、总胆固醇、TG水平、胰岛素抵抗指数和RBP4水平低于有内脏肥胖的肥胖女性。此外,尽管身体脂肪增加,但无内脏肥胖的肥胖女性的TG、胰岛素抵抗指数和血清RBP4水平低于有内脏肥胖的非肥胖女性。通过逐步多元回归分析,内脏脂肪面积和LDL胆固醇水平独立影响RBP4水平。
我们确定血清RBP4水平与内脏脂肪和LDL胆固醇水平独立相关。这些结果表明,无论体重如何,内脏肥胖是血清RBP4水平的独立预测因素,并且RBP4可能代表内脏肥胖与心血管疾病之间的联系。