Evidence map›Paper›PMID 30817848›Full record

ReviewMolecular nutrition & food research2019

Factors Explaining Interpersonal Variation in Plasma Enterolactone Concentrations in Humans.

Elin Hålldin, Anne Kirstine Eriksen, Carl Brunius, Andreia Bento da Silva, Maria Bronze, Kati Hanhineva, Anna-Marja Aura, Rikard Landberg

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular nutrition & food research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
4.5field-weighted citation impact, top 5% of its field
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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

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  14. Gut microbiome: a novel preventive and therapeutic target for prostatic disease.Frontiers in cellular and infection microbiology · 2024
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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

8 authors at 6 institutions in 4 countries.

Elin HålldinDepartment of Molecular Science, Uppsala BioCenter, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
Anne Kirstine EriksenDepartment of Molecular Science, Uppsala BioCenter, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden.
Carl BruniusDepartment of Biology and Biological Engineering, Food and Nutrition Science, Chalmers University of Technology, Gothenburg, Sweden.
Andreia Bento da SilvaITQB-NOVA, Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal.
Maria BronzeITQB-NOVA, Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Oeiras, Portugal.
Kati HanhinevaLC-MS Metabolomics Center, Kuopio, Finland.
Anna-Marja AuraVTT Technical Research Centre of Finland Ltd, Post Office Box 1000, Tietotie 2, Espoo, FI-02044 VTT, Finland.
Rikard LandbergDepartment of Biology and Biological Engineering, Food and Nutrition Science, Chalmers University of Technology, Gothenburg, Sweden.
Chalmers University of Technology · SEUniversidade Nova de Lisboa · PTDanish Cancer Society · DKSwedish University of Agricultural Sciences · SETieto (Finland) · FIUniversity of Eastern Finland · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lignans are diphenolic plant compounds with potential health modulating properties that are absorbed to the circulation and metabolized to the enterolignans enterodiol (END) and enterolactone (ENL) by gut microbiota. Epidemiological studies have inconsistently shown that a high lignan intake and circulating ENL are associated with reduced risk of breast-, prostate-, and colorectal cancer as well as cardiovascular disease and total and cause-specific mortality. Inconsistencies can be due to interpersonal variation of ENL formation or responses. The aim of this review is to identify and evaluate the impact of factors influencing variability in plasma concentrations of the main enterolignan, ENL. The main determinants of plasma ENL concentrations are intake of lignan and lignan-rich foods, composition and activity of intestinal microflora, antimicrobial use, nutrient intake, BMI, smoking, sex, and age. Composition and activity of the intestinal microbiota appear to be the most critical factor governing interpersonal variability in plasma ENL concentration followed by the use of antibiotics. Future studies with combined data from gut microbiota and metabolomics with food intake and life style data can be used to estimate the relative contribution of the different factors to ENL concentration in quantitative terms.

Indexed as

4-ButyrolactoneAnti-Infective AgentsBody Mass IndexFemaleGastrointestinal MicrobiomeHealth StatusHumansLignansMaleNutrients2,3-bis(3'-hydroxybenzyl)butane-1,4-diol2,3-bis(3'-hydroxybenzyl)butyrolactone4-ButyrolactoneAnti-Infective AgentsLignansNutrientsdeterminantsenterolactoneinterpersonal variationlignansplasma

Identifiers

PMID30817848
PMCPMC7317467
OpenAlexW2919906835

What OpenQuestion holds

Textmetadata
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.