Division of Human Nutrition and Health, Wageningen University, Wageningen, The Netherlands.
Nottingham Digestive Diseases Centre, NIHR Nottingham Biomedical Research Centre (BRC), Nottingham University Hospitals NHS Trust and University of Nottingham, Nottingham, UK.
Neurogastroenterol Motil. 2024 Nov;36(11):e14904. doi: 10.1111/nmo.14904. Epub 2024 Aug 27.
Gastric fluid plays a key role in food digestion and drug dissolution, therefore, the amount of gastric fluid present in a fasted state may influence subsequent digestion and drug delivery. We aimed to describe intra- and interindividual variation in fasted gastric content volume (FGCV) and to determine the association with age, sex, and body size characteristics.
Data from 24 MRI studies measuring FGCV in healthy, mostly young individuals after an overnight fast were pooled. The analysis included 366 participants who had up to 6 repeated measurements, with a total of 870 measurements. Linear mixed model analysis was performed to calculate intra- and interindividual variability and to assess the effects of age, sex, weight, height, weight*height as a proxy for body size, and body mass index (BMI).
FGCV ranged from 0 to 156 mL, with a mean (± SD) value of 33 ± 25 mL. The overall coefficient of variation within the study population was 75.6%, interindividual SD was 15 mL, and the intraindividual SD was 19 mL. Age, weight, height, weight*height, and BMI had no effect on FGCV. Women had lower volumes compared to men (MD: -6 mL), when corrected for the aforementioned factors.
FGCV is highly variable, with higher intraindividual compared to interindividual variability, indicating that FGCV is subject to day-to-day and within-day variation and is not a stable personal characteristic. This highlights the importance of considering FGCV when studying digestion and drug dissolution. Exact implications remain to be studied.
胃液在食物消化和药物溶解中起着关键作用,因此空腹时胃内液量可能会影响后续的消化和药物输送。我们旨在描述空腹胃内容量(FGCV)的个体内和个体间变异性,并确定其与年龄、性别和体型特征的关系。
对 24 项 MRI 研究的数据进行了汇总,这些研究测量了健康个体在禁食一夜后空腹胃内容量。分析包括 366 名参与者,他们最多有 6 次重复测量,总共有 870 次测量。采用线性混合模型分析计算个体内和个体间的变异性,并评估年龄、性别、体重、身高、体重*身高(代表体型)和体重指数(BMI)的影响。
FGCV 范围为 0 至 156 mL,平均值(±SD)为 33±25 mL。研究人群的总体变异系数为 75.6%,个体间 SD 为 15 mL,个体内 SD 为 19 mL。年龄、体重、身高、体重*身高和 BMI 对 FGCV 无影响。在考虑了上述因素后,女性的 FGCV 体积比男性低(MD:-6 mL)。
FGCV 具有高度的变异性,个体内变异性高于个体间变异性,这表明 FGCV 受日常和日内变化的影响,而不是一个稳定的个体特征。这突出了在研究消化和药物溶解时考虑 FGCV 的重要性。确切的影响仍有待研究。