Maffeis Claudio, Fornari Elena, Morandi Anita, Piona Claudia, Tomasselli Francesca, Tommasi Mara, Marigliano Marco
Pediatric Diabetes and Metabolic Disorders Unit, Regional Center for Pediatric Diabetes, University City Hospital of Verona, P.le Stefani, 1, 37126, Verona, Italy.
Acta Diabetol. 2017 Jun;54(6):599-605. doi: 10.1007/s00592-017-0993-y. Epub 2017 Apr 18.
To test the hypothesis that diet composition, adiposity and glycometabolic control could independently contribute to an increase in the cardiovascular risk (CVR) for children/adolescents with type 1 diabetes (T1D).
One hundred and eighty children/adolescents with T1D (age range 5-18 years) were enrolled. Diet (3-day weighed dietary record), physical (height, weight, waist circumference, bioelectrical impedance analysis) and biochemical (HbA1c, lipid profile) parameters were recorded. Regression models, using non-HDL cholesterol (a gross index of CVR) as the dependent variable and HbA1c (mmol/mol), fat mass (FM) %, lipid-to-carbohydrate intake ratio as independent ones, were calculated.
Non-HDL cholesterol was significantly associated with adiposity (FM%; r = 0.27, 95% CI 0.13-0.43), body fat distribution (waist-to-height ratio; r = 0.16, 95% CI 0.02-0.31), lipid intake [% of energy intake (EI)] (r = 0.25, 95% CI 0.11-0.41), carbohydrate intake (% EI; r = -0.24, 95% CI 0.10-0.40), lipid-to-carbohydrate intake ratio (r = 0.26, 95% CI 0.12-0.42) and blood glucose control (HbA1c; r = 0.24, 95% CI 0.10-0.40). A p value cutoff of 0.10 was used for covariates to be included in the regression analysis. Multiple regression analysis showed that adiposity (FM%), blood glucose control (HbA1c) and lipid-to-carbohydrate intake ratio independently contributed to explaining the inter-individual variability of non-HDL cholesterol (R = 0.163, p < 0.05).
Adiposity and lipid-to-carbohydrate intake ratio affect non-HDL cholesterol, a gross index of CVR, regardless of HbA1c, in children and adolescents with T1D. Intervention to reduce CVR in T1D patients should focus not only on glycometabolic control but also on adiposity and diet composition.
检验饮食构成、肥胖及糖代谢控制是否能独立导致1型糖尿病(T1D)儿童/青少年的心血管风险(CVR)增加这一假设。
招募了180名T1D儿童/青少年(年龄范围5 - 18岁)。记录饮食(3天称重饮食记录)、身体指标(身高、体重、腰围、生物电阻抗分析)和生化指标(糖化血红蛋白、血脂谱)。计算回归模型,以非高密度脂蛋白胆固醇(CVR的总体指标)作为因变量,糖化血红蛋白(mmol/mol)、脂肪量(FM)%、脂质与碳水化合物摄入比作为自变量。
非高密度脂蛋白胆固醇与肥胖(FM%;r = 0.27,95%CI 0.13 - 0.43)、体脂分布(腰高比;r = 0.16,95%CI 0.02 - 0.31)、脂质摄入[能量摄入(EI)的%](r = 0.25,95%CI 0.11 - 0.41)、碳水化合物摄入(%EI;r = -0.24,95%CI 0.10 - 0.40)、脂质与碳水化合物摄入比(r = 0.26,95%CI 0.12 - 0.42)及血糖控制(糖化血红蛋白;r = 0.24,95%CI 0.10 - 0.40)显著相关。在回归分析中,协变量的p值临界值设为0.10。多元回归分析显示,肥胖(FM%)、血糖控制(糖化血红蛋白)和脂质与碳水化合物摄入比可独立解释非高密度脂蛋白胆固醇的个体间变异性(R = 0.163,p < 0.05)。
在T1D儿童和青少年中,肥胖及脂质与碳水化合物摄入比会影响非高密度脂蛋白胆固醇(CVR的总体指标),且不受糖化血红蛋白影响。降低T1D患者CVR的干预措施不仅应关注糖代谢控制,还应关注肥胖和饮食构成。