空腹胃内容量的个体内和个体间差异

Julia J.M. Roelofs, Guido Camps, Louise M. Leenders, Luca Marciani, Robin C. Spiller, Elise J.M. van Eijnatten, Jaber Alyami, Ruoxuan Deng, Daniela Freitas, Michael Grimm, Leila J. Karhunen, Shanthi Krishnasamy, Steven Le Feunteun, Dileep N. Lobo, Alan R. Mackie, Morwarid Mayar, werner Weitschies, Paul A.M. Smeets
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摘要

背景:胃液在食物消化和药物溶解过程中起着关键作用,因此,空腹状态下的胃液量可能会影响随后的消化和给药。我们旨在描述空腹胃内容量(FGCV)的个体内和个体间差异,并确定其与年龄、性别和体型特征的关联:我们汇总了 24 项核磁共振成像研究的数据,这些研究测量了健康人(大多为年轻人)在一夜禁食后的空腹胃容积(FGCV)。分析包括366名参与者,共进行了870次测量。线性混合模型分析计算了个体内和个体间的变异性,并评估了年龄、性别、体重、身高、体重*身高(作为体型的替代指标)和体重指数(BMI)的影响:FGCV的范围从0到156毫升不等,平均(标清)值为33毫升(25毫升)。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*身高和体重指数对 FGCV 没有影响。在对上述因素进行校正后,女性的血容量低于男性(MD:-6 mL):结论:FGCV 的可变性很高,个体内的可变性高于个体间的可变性,这表明 FGCV 受日常和日内变化的影响,并不是一个稳定的个人特征。这突出了在研究消化和药物溶解时考虑 FGCV 的重要性。具体影响还有待研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intra- and interindividual variability in fasted gastric content volume
Background: 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. Methods: Data from 24 MRI studies measuring FGCV in healthy, mostly young individuals after an overnight fast were pooled. Analysis included 366 participants 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). Results: FGCV ranged from 0 to 156 mL, with a mean (SD) value of 33 mL (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. Conclusion: 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.
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