Program in Nutritional Metabolism and Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA 02114, USA.
Clin Endocrinol (Oxf). 2012 Sep;77(3):385-90. doi: 10.1111/j.1365-2265.2011.04284.x.
The relationship of monocyte/macrophage activation to insulin resistance in obesity is unknown.
To investigate a marker of macrophage activation, soluble CD163 (sCD163), in relationship to insulin resistance and metabolic parameters in obese and normal-weight subjects.
Ninety-five healthy subjects (65 obese and 30 normal-weight) were studied. Plasma concentrations of sCD163 were assessed, as well as markers of glucose homeostasis, anthropometrics, cytokines and adipokines. The relationships between sCD163 and these parameters were investigated, and multiple regression modelling assessing the contribution of sCD163 to insulin resistance (HOMA-IR) was performed.
Soluble CD163 was significantly increased in obese subjects compared with normal-weight controls [974 (657, 1272) ng/ml vs 599 (423, 892) ng/ml, median (IQR); P < 0·0001]. sCD163 was strongly associated with HOMA-IR (Spearman's ρ = 0·37, P = 0·0003) and other metabolic parameters. In multiple regression modelling for log HOMA-IR, sCD163 remained significantly associated (P = 0·005) controlling for known mediators of insulin resistance including age, gender, visceral adiposity and inflammatory markers (model R(2) = 0·54, P < 0·0001). Additional nested multiple regression models for log HOMA-IR showed that sCD163 added more than other adipokines and inflammatory markers to the prediction of HOMA-IR.
Monocyte/macrophage activation, as reflected by sCD163 levels, is strongly associated with HOMA-IR in normal-weight and obese subjects after controlling for known mediators of insulin resistance. Moreover, sCD163 adds to standard risk markers for predicting insulin resistance. These data suggest that monocyte/macrophage activation may be an important determinant of insulin resistance in obesity.
单核细胞/巨噬细胞激活与肥胖相关的胰岛素抵抗之间的关系尚不清楚。
研究肥胖和正常体重受试者中一种巨噬细胞激活标志物可溶性 CD163(sCD163)与胰岛素抵抗及代谢参数的关系。
研究了 95 名健康受试者(65 名肥胖和 30 名正常体重)。评估了 sCD163 的血浆浓度,以及葡萄糖稳态、人体测量学、细胞因子和脂肪因子的标志物。研究了 sCD163 与这些参数的关系,并进行了多元回归模型评估 sCD163 对胰岛素抵抗(HOMA-IR)的贡献。
与正常体重对照组相比,肥胖受试者的 sCD163 显著升高[974(657,1272)ng/ml 比 599(423,892)ng/ml,中位数(IQR);P<0.0001]。sCD163 与 HOMA-IR 及其他代谢参数呈强烈相关(Spearman's ρ=0.37,P=0.0003)。在对数 HOMA-IR 的多元回归模型中,sCD163 仍然与已知的胰岛素抵抗调节剂(包括年龄、性别、内脏脂肪和炎症标志物)相关(P=0.005)(模型 R²=0.54,P<0.0001)。对数 HOMA-IR 的额外嵌套多元回归模型显示,sCD163 比其他脂肪因子和炎症标志物对 HOMA-IR 的预测更有意义。
在控制已知的胰岛素抵抗调节剂后,单核细胞/巨噬细胞激活,反映在 sCD163 水平上,与正常体重和肥胖受试者的 HOMA-IR 强烈相关。此外,sCD163 增加了预测胰岛素抵抗的标准风险标志物。这些数据表明,单核细胞/巨噬细胞激活可能是肥胖相关胰岛素抵抗的一个重要决定因素。