Swinburn B A, Ravussin E
Department of Community Health, University of Auckland, New Zealand.
Baillieres Clin Endocrinol Metab. 1994 Jul;8(3):527-48. doi: 10.1016/s0950-351x(05)80285-x.
In general, obesity is a state of high energy stores, high energy intake, and high energy expenditure. The high energy expenditure is largely due to the increased fat-free mass. The failure to find a positive relationship between reported energy intake and body size reflects a greater under-reporting of calorie intake among obese individuals. Obesity, therefore, develops as a consequence of a chronic imbalance between intake and expenditure, although the cause of this is not apparent from the energy balance equation. However, this equation can be dissected into its component nutrient balance equations because net de novo lipogenesis is negligible in free-living humans. Fat calories are handled very differently from non-fat calories. Non-fat nutrient oxidation rates rise and fall to match the fluctuations in non-fat intake so that non-fat calorie balance is actively maintained. In contrast, changes in fat intake do not acutely affect fat oxidation but are matched by changes in storage. Therefore, within the fat balance equation there is ample scope for a chronic imbalance between fat intake and oxidation. Also, there is some evidence that carbohydrate balance may be an important signal for hunger and satiety. These concepts imply that, under free-living, ad libitum eating conditions, changes in nutrient intake composition (e.g. an increased proportion of fat in the diet) or changes in nutrient oxidation composition (e.g. a decrease in the proportion of fat oxidized) will lead to body weight change (in these cases, to weight gain). Considering obesity as a consequence of normal physiology (with its normal variation between individuals) in a 'pathological' environment (high fat diet, low exercise) offers an important perspective for explaining the interpopulation and interindividual differences in obesity and for formulating treatment and prevention options. Low energy expenditure (relative to body size), high respiratory quotient and insulin sensitivity have been shown to be predictors of weight gain, although upon gaining weight these metabolic factors tend to 'normalize'. Metabolic responses to underfeeding or overfeeding are largely predictable from the changes in calorie intake and changes in body composition, but some adaptive changes may occur.
一般来说,肥胖是一种能量储存高、能量摄入高和能量消耗高的状态。高能量消耗主要归因于去脂体重的增加。未能在报告的能量摄入与体型之间找到正相关关系,这反映出肥胖个体中卡路里摄入量的漏报情况更为严重。因此,肥胖是摄入与消耗之间长期失衡的结果,尽管从能量平衡方程中并不明显看出其原因。然而,由于在自由生活的人类中从头脂肪生成净值可忽略不计,这个方程可以分解为其组成的营养平衡方程。脂肪热量与非脂肪热量的处理方式非常不同。非脂肪营养物质的氧化速率会随着非脂肪摄入量的波动而上升和下降,从而积极维持非脂肪热量平衡。相比之下,脂肪摄入量的变化不会急性影响脂肪氧化,而是与储存量的变化相匹配。因此,在脂肪平衡方程中,脂肪摄入与氧化之间长期失衡的空间很大。此外,有一些证据表明碳水化合物平衡可能是饥饿和饱腹感的重要信号。这些概念意味着,在自由生活、随意进食的条件下,营养摄入组成的变化(例如饮食中脂肪比例增加)或营养氧化组成的变化(例如氧化脂肪比例降低)将导致体重变化(在这些情况下,体重增加)。将肥胖视为在“病理”环境(高脂肪饮食、低运动量)中正常生理(个体之间存在正常差异)的结果,为解释肥胖的人群间和个体间差异以及制定治疗和预防方案提供了一个重要视角。低能量消耗(相对于体型)、高呼吸商和胰岛素敏感性已被证明是体重增加的预测指标,尽管体重增加后这些代谢因素往往会“正常化”。对进食不足或进食过量的代谢反应在很大程度上可根据卡路里摄入量的变化和身体组成的变化来预测,但可能会发生一些适应性变化。