Mohn Nutrition Research Laboratory, Centre for Nutrition, Department of Clinical Science, University of Bergen, Bergen, Norway.
Department of Nutrition, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Br J Nutr. 2024 Oct 14;132(7):851-861. doi: 10.1017/S0007114524001934. Epub 2024 Oct 18.
To improve the interpretation and utilisation of blood lipids, ketones and acylcarnitine concentrations as biomarkers in clinical assessments, more information is needed on their dynamic alterations in response to dietary intake and fasting. The aim of this intervention study was to characterise the changes in serum lipid, ketone and acylcarnitine concentrations 24 h after a standardised breakfast meal. Thirty-four healthy subjects (eighteen males and sixteen females) aged 20-30 years were served a breakfast meal (∼500 kcal, 36 E% fat, 46 E% carbohydrates, 16 E% protein, 2E% fibre), after which they consumed only water for 24 h. Blood samples were drawn before and at thirteen standardised timepoints after the meal. Metabolite concentrations were plotted as a function of time since the completion of the breakfast meal. Results demonstrated that concentrations of HDL-cholesterol and LDL-cholesterol decreased until ∼2 h (-4 % for both), while TAG concentrations peaked at 3 h (+27 %). Acetoacetate and -hydroxybutyrate were highest 24 h after the meal (+433 and +633 %, respectively). Acetylcarnitine, butyrylcarnitine, hexanoylcarnitine, octanoylcarnitine, decanoylcarnitine and dodecanoylcarnitine reached the lowest values at 60 min (decreases ranging from -47 to -70 %), before increasing and peaking at 24 h after the meal (increases ranging from +86 to +120 %). Our findings suggest that distinguishing between fasting and non-fasting blood samples falls short of capturing the dynamics in lipid, ketone, carnitine and acylcarnitine concentrations. To enhance the utility of serum acylcarnitine analyses, we strongly recommend accounting for the specific time since the last meal at the time of blood sampling.
为了提高血脂、酮体和酰基肉碱浓度作为临床评估生物标志物的解释和利用,需要更多关于它们在饮食摄入和禁食时动态变化的信息。本干预研究的目的是描述标准化早餐后 24 小时血清脂质、酮体和酰基肉碱浓度的变化。34 名年龄在 20-30 岁的健康受试者(18 名男性和 16 名女性)食用了一顿早餐(约 500 卡路里,36%脂肪,46%碳水化合物,16%蛋白质,2%纤维),之后他们在 24 小时内仅饮水。在餐前和餐后 13 个标准化时间点抽取血样。将代谢物浓度绘制为餐后时间的函数。结果表明,HDL-胆固醇和 LDL-胆固醇的浓度在 2 小时内下降(两者均下降 4%),而 TAG 浓度在 3 小时时达到峰值(增加 27%)。乙酰乙酸和β-羟丁酸在餐后 24 小时时最高(分别增加 433%和 633%)。乙酰肉碱、丁酰肉碱、己酰肉碱、辛酰肉碱、癸酰肉碱和十二酰肉碱在 60 分钟时达到最低值(下降幅度为 47%至 70%),然后在餐后 24 小时时增加并达到峰值(增加幅度为 86%至 120%)。我们的发现表明,区分空腹和非空腹血样并不能捕捉脂质、酮体、肉碱和酰基肉碱浓度的动态变化。为了提高血清酰基肉碱分析的实用性,我们强烈建议在采血时考虑上次进食后的具体时间。