Evidence map›Paper›PMID 31187866›Full record

ArticleThe Journal of nutrition2019

Addition of Vitamin A Intake Data during Compartmental Modeling of Retinol Kinetics in Theoretical Humans Leads to Accurate Prediction of Vitamin A Total Body Stores and Kinetic Parameters in Studies of Reasonable Duration.

Jennifer Lynn Ford, Joanne Balmer Green, Michael H Green

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Article in The Journal of nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

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8citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jennifer Lynn FordDepartment of Nutritional Sciences, College of Health and Human Development, The Pennsylvania State University, University Park, PA, USA.
Joanne Balmer GreenDepartment of Nutritional Sciences, College of Health and Human Development, The Pennsylvania State University, University Park, PA, USA.
Michael H GreenDepartment of Nutritional Sciences, College of Health and Human Development, The Pennsylvania State University, University Park, PA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMathematical modeling of theoretical data has been used to validate experimental protocols and methods in several fields.

objectivesWe hypothesized that adding dietary vitamin A intake data as an input during compartmental modeling of retinol kinetics would lead to accurate prediction of vitamin A total body stores (TBS) at 2 specified study lengths and would reduce study duration required to accurately define the system.

methodsWe generated reference values for state variables (including TBS and intake) and kinetic parameters for 12 theoretical individuals (4 each of children, younger adults, and older adults) based on modeling plasma retinol tracer data for 365 d. We compared TBS predictions using data to 28 d (children) or 56 d (adults) without and with intake included in the model to reference values for each subject. Then, by truncating data sets from 365 d, we determined the shortest study duration required to accurately define the system without and with inclusion of vitamin A intake.

resultsReference values for TBS ranged from 30 to 3023 µmol. Study durations of 28 and 56 d were sufficient to accurately predict TBS for 6 of the 12 subjects without intake; adding intake resulted in accurate predictions of TBS for all individuals. When intake was not included as a modeling input, durations of 35-310 d were required to define the system; inclusion of intake data substantially reduced the time required to 10-42 d.

conclusionsInclusion of vitamin A intake as additional data input when modeling vitamin A kinetics allows investigators to accurately predict TBS and define the vitamin A system in studies of reasonable length (4 wk in children and 8 wk in adults). Because it is generally possible to obtain estimates/measures of intake, including such data increases confidence in model predictions while also making studies more feasible.

Indexed as

Models, BiologicalAdultChild, PreschoolComputer SimulationFemaleHumansInfantMaleMiddle AgedReference ValuesTime FactorsVitamin AYoung AdultVitamin Adietary vitamin A intakemodel-based compartmental analysistheoretical humanstracer kineticsvitamin A assessmentvitamin A total body storesWinSAAM

Identifiers

PMID31187866
PMCPMC6825818

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.