Department of Research and Evaluation, Kaiser Permanente Southern California, Pasadena, CA, USA.
J Nutr. 2013 Apr;143(4):479-85. doi: 10.3945/jn.112.170449. Epub 2013 Jan 23.
Consumption of energy-dense, nutrient-poor foods has contributed to the rising incidence of obesity and may underlie insulin resistance and β-cell dysfunction. Macronutrient intake patterns were examined in relation to anthropometric and metabolic traits in participants of BetaGene, a family-based study of obesity, insulin resistance, and β-cell dysfunction in Mexican Americans. Dietary intake, body composition, insulin sensitivity (SI), and β-cell function [Disposition Index (DI)] were assessed by food-frequency questionnaires, dual-energy X-ray absorptiometry, and intravenous glucose-tolerance tests, respectively. Patterns of macronutrient intake were identified by using a K-means model based on the proportion of total energy intake per day attributable to carbohydrate, fat, and protein and were tested for association with anthropometric and metabolic traits. Among 1150 subjects aged 18-65 y (73% female), tertiles of fat intake were associated with greater adiposity and lower SI, after adjustment for age, sex, and daily energy intake. Moreover, 3 distinct dietary patterns were identified: "high fat" (35% fat, 44% carbohydrate, 21% protein; n = 238), "moderate fat" (28% fat, 54% carbohydrate, 18% protein; n = 520), and "low fat" (20% fat, 65% carbohydrate, 15% protein; n = 392). Compared with the low-fat group, the high-fat group had higher age- and sex-adjusted mean body mass index, body fat percentage, and trunk fat and lower SI and DI. Further adjustment for daily energy intake by matching individuals across dietary pattern groups yielded similar results. None of the observed associations were altered after adjustment for physical activity; however, associations with SI and DI were attenuated after adjustment for adiposity. These findings suggest that high-fat diets may contribute to increased adiposity and concomitant insulin resistance and β-cell dysfunction in Mexican Americans.
能量密集、营养贫乏的食物摄入与肥胖的发生率上升有关,并且可能是导致胰岛素抵抗和β细胞功能障碍的原因。在 BetaGene 研究中,我们对 1150 名 18-65 岁的(73%为女性)墨西哥裔美国人进行了基于家族的肥胖、胰岛素抵抗和β细胞功能障碍的研究,检测了宏量营养素摄入模式与人体测量和代谢特征的关系。通过基于每日总能量摄入中碳水化合物、脂肪和蛋白质所占比例的 K-均值模型确定宏量营养素摄入模式,并对其与人体测量和代谢特征的相关性进行了测试。结果显示,在调整年龄、性别和每日能量摄入后,脂肪摄入量的三分位数与肥胖程度增加和胰岛素敏感性降低有关。此外,还确定了 3 种不同的饮食模式:“高脂肪”(35%脂肪,44%碳水化合物,21%蛋白质;n = 238)、“中等脂肪”(28%脂肪,54%碳水化合物,18%蛋白质;n = 520)和“低脂肪”(20%脂肪,65%碳水化合物,15%蛋白质;n = 392)。与低脂肪组相比,高脂肪组的年龄和性别调整后的平均体重指数、体脂百分比、躯干脂肪含量更高,胰岛素敏感性和处置指数更低。通过匹配饮食模式组内的个体来对每日能量摄入进行进一步调整后,得到了类似的结果。在调整体力活动后,没有观察到任何关联发生改变;然而,调整肥胖程度后,与胰岛素敏感性和处置指数的关联减弱。这些发现表明,高脂肪饮食可能导致墨西哥裔美国人肥胖程度增加以及伴随的胰岛素抵抗和β细胞功能障碍。