Evidence map›Paper›PMID 31642982›Full record

ReviewEuropean journal of nutrition2019

Future prospects for dissecting inter-individual variability in the absorption, distribution and elimination of plant bioactives of relevance for cardiometabolic endpoints.

Rikard Landberg, Claudine Manach, Frederiek-Maarten Kerckhof, Anne-Marie Minihane, Rasha Noureldin M Saleh, Baukje De Roos, Francisco Tomas-Barberan, Christine Morand, Tom Van de Wiele

Abstract readReview
In one paragraph

Review in European journal of nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  9. Nutritional and dietary clinical trials for Parkinson's disease: a narrative review.Journal of neural transmission (Vienna, Austria : 1996) · 2025
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  13. Allyl Aryl Ether Cleavage byMicrobiology spectrum · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Rikard LandbergDepartment of Biology and Biological Engineering, Food and Nutrition Science, Chalmers University of Technology, 412 96, Gothenburg, Sweden. Rikard.landberg@chalmers.se.
Claudine ManachUniversité Clermont Auvergne, INRA, UNH, Unité de Nutrition Humaine, CRNH Auvergne, Clermont-Ferrand, France.
Frederiek-Maarten KerckhofCenter for Microbial Ecology and Technology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0002-4472-6810
Anne-Marie MinihaneDepartment of Nutrition and Preventive Medicine, Norwich Medical School, University of East Anglia (UEA), Norwich, UK.
Rasha Noureldin M SalehDepartment of Nutrition and Preventive Medicine, Norwich Medical School, University of East Anglia (UEA), Norwich, UK.
Baukje De RoosUniversity of Aberdeen, the Rowett Institute, Aberdeen, UK.ORCID http://orcid.org/0000-0002-2750-3914
Francisco Tomas-BarberanFood and Health Laboratory, Research Group on Quality, Safety, and Bioactivity of Plant Foods, CEBAS-CSIC, Campus de Espinardo, Murcia, Spain.ORCID http://orcid.org/0000-0002-0790-1739
Christine MorandUniversité Clermont Auvergne, INRA, UNH, Unité de Nutrition Humaine, CRNH Auvergne, Clermont-Ferrand, France.
Tom Van de WieleCenter for Microbial Ecology and Technology, Faculty of Bioscience Engineering, Ghent University, Ghent, Belgium.ORCID http://orcid.org/0000-0001-6854-5689

Funding

EU - COST Action FA-1403 (2014-2018) FA1403
6 · The paper itself

Abstract

purposeThe health-promoting potential of food-derived plant bioactive compounds is evident but not always consistent across studies. Large inter-individual variability may originate from differences in digestion, absorption, distribution, metabolism and excretion (ADME). ADME can be modulated by age, sex, dietary habits, microbiome composition, genetic variation, drug exposure and many other factors. Within the recent COST Action POSITIVe, large-scale literature surveys were undertaken to identify the reasons and extent of inter-individual variability in ADME of selected plant bioactive compounds of importance to cardiometabolic health. The aim of the present review is to summarize the findings and suggest a framework for future studies designed to investigate the etiology of inter-individual variability in plant bioactive ADME and bioefficacy.

resultsFew studies have reported individual data on the ADME of bioactive compounds and on determinants such as age, diet, lifestyle, health status and medication, thereby limiting a mechanistic understanding of the main drivers of variation in ADME processes observed across individuals. Metabolomics represent crucial techniques to decipher inter-individual variability and to stratify individuals according to metabotypes reflecting the intrinsic capacity to absorb and metabolize bioactive compounds.

conclusionA methodological framework was developed to decipher how the contribution from genetic variants or microbiome variants to ADME of bioactive compounds can be predicted. Future study design should include (1) a larger number of study participants, (2) individual and full profiling of all possible determinants of internal exposure, (3) the presentation of individual ADME data and (4) incorporation of omics platforms, such as genomics, microbiomics and metabolomics in ADME and efficacy studies.

Indexed as

Biological Variation, PopulationCardiovascular SystemDiet, VegetarianHumansMetabolomicsPhytochemicalsPlants, EdiblePhytochemicalsCardiometabolicInter-individual variationPersonalized nutritionPlant bioactive compounds

Identifiers

PMID31642982
PMCPMC6851035

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.