Schwander Flurina, Kopf-Bolanz Katrin A, Buri Caroline, Portmann Reto, Egger Lotti, Chollet Magali, McTernan Philip G, Piya Milan K, Gijs Martin A M, Vionnet Nathalie, Pralong François, Laederach Kurt, Vergères Guy
Institute of Food Science, Agroscope, Federal Office of Agriculture, Berne, Switzerland.
Division of Endocrinology, Diabetes, and Clinical Nutrition, University Hospital of Berne, Berne, Switzerland.
J Nutr. 2014 Oct;144(10):1517-23. doi: 10.3945/jn.114.193565. Epub 2014 May 8.
A dose-response strategy may not only allow investigation of the impact of foods and nutrients on human health but may also reveal differences in the response of individuals to food ingestion based on their metabolic health status. In a randomized crossover study, we challenged 19 normal-weight (BMI: 20-25 kg/m(2)) and 18 obese (BMI: >30 kg/m(2)) men with 500, 1000, and 1500 kcal of a high-fat (HF) meal (60.5% energy from fat). Blood was taken at baseline and up to 6 h postprandially and analyzed for a range of metabolic, inflammatory, and hormonal variables, including plasma glucose, lipids, and C-reactive protein and serum insulin, glucagon-like peptide-1, interleukin-6 (IL-6), and endotoxin. Insulin was the only variable that could differentiate the postprandial response of normal-weight and obese participants at each of the 3 caloric doses. A significant response of the inflammatory marker IL-6 was only observed in the obese group after ingestion of the HF meal containing 1500 kcal [net incremental AUC (iAUC) = 22.9 ± 6.8 pg/mL × 6 h, P = 0.002]. Furthermore, the net iAUC for triglycerides significantly increased from the 1000 to the 1500 kcal meal in the obese group (5.0 ± 0.5 mmol/L × 6 h vs. 6.0 ± 0.5 mmol/L × 6 h; P = 0.015) but not in the normal-weight group (4.3 ± 0.5 mmol/L × 6 h vs. 4.8 ± 0.5 mmol/L × 6 h; P = 0.31). We propose that caloric dose-response studies may contribute to a better understanding of the metabolic impact of food on the human organism. This study was registered at clinicaltrials.gov as NCT01446068.
剂量反应策略不仅可以用于研究食物和营养素对人体健康的影响,还可能揭示个体根据其代谢健康状况对食物摄入反应的差异。在一项随机交叉研究中,我们让19名体重正常(BMI:20 - 25 kg/m²)和18名肥胖(BMI:>30 kg/m²)男性分别摄入500、1000和1500千卡的高脂肪(HF)餐(脂肪提供60.5%的能量)。在基线和餐后6小时内采集血液,分析一系列代谢、炎症和激素变量,包括血浆葡萄糖、脂质、C反应蛋白以及血清胰岛素、胰高血糖素样肽 - 1、白细胞介素 - 6(IL - 6)和内毒素。胰岛素是唯一能在3种热量剂量下区分体重正常和肥胖参与者餐后反应的变量。仅在肥胖组摄入含1500千卡的HF餐后观察到炎症标志物IL - 6有显著反应[净增量AUC(iAUC)= 22.9 ± 6.8 pg/mL × 6小时,P = 0.002]。此外,肥胖组中甘油三酯的净iAUC从1000千卡餐到1500千卡餐显著增加(5.0 ± 0.5 mmol/L × 6小时对6.0 ± 0.5 mmol/L × 6小时;P = 0.015),而体重正常组未出现这种情况(4.3 ± 0.5 mmol/L × 6小时对4.8 ± 0.5 mmol/L × 6小时;P = 0.31)。我们认为热量剂量反应研究可能有助于更好地理解食物对人体代谢产生的影响。本研究在clinicaltrials.gov上注册,注册号为NCT01446068。