Intra‐ and interindividual variability in fasted gastric content volume

Author:

Roelofs Julia J. M.1ORCID,Camps Guido1ORCID,Leenders Louise M.1ORCID,Marciani Luca2ORCID,Spiller Robin C.2ORCID,Van Eijnatten Elise J. M.1ORCID,Alyami Jaber23ORCID,Deng Ruoxuan1ORCID,Freitas Daniela4ORCID,Grimm Michael5ORCID,Karhunen Leila J.6ORCID,Krishnasamy Shanthi2,Le Feunteun Steven7ORCID,Lobo Dileep N.28ORCID,Mackie Alan R.9ORCID,Mayar Morwarid1ORCID,Weitschies Werner6ORCID,Smeets Paul A. M.1ORCID

Affiliation:

1. Division of Human Nutrition and Health Wageningen University Wageningen The Netherlands

2. Nottingham Digestive Diseases Centre, NIHR Nottingham Biomedical Research Centre (BRC) Nottingham University Hospitals NHS Trust and University of Nottingham Nottingham UK

3. Radiological Sciences Department, Faculty of Applied Medical Sciences King Abdulaziz University Jeddah Saudi Arabia

4. Université Paris‐Saclay, INRAE AgroParisTech, UMR SayFood Thiverval‐Grignon France

5. Institute of Pharmacy, Center of Drug Absorption and Transport University of Greifswald Greifswald Germany

6. Institute of Public Health and Clinical Nutrition University of Eastern Finland Kuopio Finland

7. INRAE, Institut Agro Rennes France

8. Division of Surgery, Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

9. Food Colloids and Processing Group, School of Food Science and Nutrition University of Leeds Leeds UK

Abstract

AbstractBackgroundGastric 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.MethodsData 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).ResultsFGCV 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.ConclusionFGCV 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.

Publisher

Wiley

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