Guzzetti C, Pilia S, Ibba A, Loche S
Pediatric Endocrinology Unit, Microcitemico Hospital, ASL Cagliari, Via Jenner, 09121, Cagliari, Italy.
J Endocrinol Invest. 2014 Jan;37(1):51-6. doi: 10.1007/s40618-013-0014-0. Epub 2014 Jan 8.
In obese subjects it has been shown that cortisol (F) contributes to the reduction in insulin sensitivity, suggesting a role in the development of the metabolic syndrome (MS).
The aim of this retrospective study was to evaluate the relationship between F and components of MS in 1,027 obese children and adolescents.
Waist circumference, systolic and diastolic blood pressure (SP, DP), F, serum glucose (Glyc), cholesterol HDL, triglycerides and homeostatic model assessment (HOMA index) were evaluated in all subjects. MS was defined according to the International Diabetes Federation criteria. Accordingly, patients were subdivided into three age groups: 6-10, 10-16 and >16 years.
In univariate regression analysis, F was correlated with Glyc, SP and HOMA in groups 1 and 2, with DP in Group 2. In multivariate regression analysis including age, sex, puberty, BMI-SDS and F as independent variables and one of the component of the MS as the dependent variable, F was a weak predictor of the variability when DP and Glyc were introduced as dependent variables in Group 2 and when SP was introduced as dependent variable both in groups 1 and 2. When patients were subdivided into subgroups according to the IDF criteria, in Group 2 patients with one or more components of the MS had higher F concentrations.
In this cohort of obese children and adolescents, F was weakly associated with components of the MS. These findings do not support a major role for F in the development of MS.
在肥胖受试者中,已表明皮质醇(F)会导致胰岛素敏感性降低,提示其在代谢综合征(MS)的发生发展中起作用。
本回顾性研究的目的是评估1027名肥胖儿童和青少年中F与MS各组分之间的关系。
对所有受试者评估腰围、收缩压和舒张压(SP、DP)、F、血清葡萄糖(Glyc)、高密度脂蛋白胆固醇、甘油三酯和稳态模型评估(HOMA指数)。MS根据国际糖尿病联盟标准定义。据此,将患者分为三个年龄组:6 - 10岁、10 - 16岁和>16岁。
在单变量回归分析中,F在第1组和第2组与Glyc、SP和HOMA相关,在第2组与DP相关。在多变量回归分析中,将年龄、性别、青春期、BMI - SDS和F作为自变量,MS的一个组分作为因变量,当在第2组将DP和Glyc作为因变量以及在第1组和第2组将SP作为因变量引入时,F是变异性的弱预测因子。当根据IDF标准将患者分为亚组时,在第2组中患有一个或多个MS组分的患者F浓度更高。
在这组肥胖儿童和青少年中,F与MS的组分弱相关。这些发现不支持F在MS发生发展中起主要作用。