Evidence map›Paper›PMID 28077379›Full record

Trial reportThe American journal of clinical nutrition2017

Effects of supplementation with nondigestible carbohydrates on fecal calprotectin and on epigenetic regulation of SFRP1 expression in the large-bowel mucosa of healthy individuals.

Fiona C Malcomson, Naomi D Willis, Iain McCallum, Long Xie, Idoia Ibero-Baraibar, Wing C Leung, Seamus Kelly, D Michael Bradburn, Nigel J Belshaw, Ian T Johnson and 1 more

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The American journal of clinical nutrition, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01214681 (Chemoprevention of Colorectal Cancer), which is not on this map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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.

NCT01214681 naunknown statusnot on this map

Chemoprevention of Colorectal Cancer: the Role of Non-digestible Carbohydrates

TypeinterventionalSponsorNewcastle UniversityRan2010 to 2012Enrolled75ConditionsColorectal CancerArmsMaltodextrin and Amioca starch, Hi-maize 260, Polydextrose, Hi-maize 260 and polydextrose
3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Review
  8. Article
  9. Crosstalk between Resveratrol and Gut Barrier: A Review.International journal of molecular sciences · 2022
    Review
  10. Epigenetics ofCancers · 2020
    Review
  11. Article
  12. Article
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

11 authors at 4 institutions in 1 country.

Fiona C MalcomsonHuman Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, United Kingdom.ORCID 0000-0001-5072-7644
Naomi D WillisHuman Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, United Kingdom.
Iain McCallumHuman Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, United Kingdom.
Long XieHuman Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, United Kingdom.
Idoia Ibero-BaraibarHuman Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, United Kingdom.
Wing C LeungInstitute of Food Research, Norwich Research Park, Norwich, Norfolk, United Kingdom.
Seamus KellyNorthumbria Healthcare National Health Service Foundation Trust, North Shields, United Kingdom; and.
D Michael BradburnNorthumbria Healthcare National Health Service Foundation Trust, Ashington, United Kingdom.
Nigel J BelshawInstitute of Food Research, Norwich Research Park, Norwich, Norfolk, United Kingdom.
Ian T JohnsonInstitute of Food Research, Norwich Research Park, Norwich, Norfolk, United Kingdom.
John C MathersHuman Nutrition Research Centre, Institute of Cellular Medicine, Newcastle University, Campus for Ageing and Vitality, Newcastle upon Tyne, United Kingdom; john.mathers@newcastle.ac.uk.ORCID 0000-0003-3406-3002
Newcastle University · GBNorwich Research Park · GBNational Health Service · GBNewcastle Hospitals - Campus for Ageing and Vitality · GB

Funding

Biotechnology and Biological Sciences Research Council BB/H005013/1Biotechnology and Biological Sciences Research Council BB/H005021/1Medical Research Council G0700718Medical Research Council MR/L016354/1
6 · The paper itself

Abstract

backgroundHyperactive Wnt signaling is frequently observed in colorectal cancer. Higher intakes of dietary fiber [nondigestible carbohydrates (NDCs)] and the fermentation product butyrate are protective against colorectal cancer and may exert their preventative effects via modulation of the Wnt pathway.

objectivesWe investigated the effects of supplementing healthy individuals with 2 NDCs [resistant starch (RS) and polydextrose] on fecal calprotectin concentrations and Wnt pathway-related gene expression. In addition, we determined whether effects on secreted frizzled-related protein 1 (SFRP1) expression are mediated via the epigenetic mechanisms DNA methylation and microRNA expression.

designIn a randomized, double-blind, placebo-controlled trial (the Dietary Intervention, Stem cells and Colorectal Cancer (DISC) Study), 75 healthy participants were supplemented with RS and/or polydextrose or placebo for 50 d in a 2 × 2 factorial design. Pre- and postintervention stool samples and rectal mucosal biopsies were collected and used to quantify calprotectin and expression of 12 Wnt-related genes, respectively. The expression of 10 microRNAs predicted to target SFRP1 was also quantified by quantitative reverse transcriptase-polymerase chain reaction, and DNA methylation was quantified at 7 CpG sites within the SFRP1 promoter region by pyrosequencing.

resultsNDC supplementation did not affect fecal calprotectin concentration. SFRP1 mRNA expression was reduced by both RS (P = 0.005) and polydextrose (P = 0.053). RS and polydextrose did not affect SFRP1 methylation or alter the expression of 10 microRNAs predicted to target SFRP1. There were no significant interactions between RS and polydextrose.

conclusionsRS and polydextrose supplementation did not affect fecal calprotectin concentrations. Downregulation of SFRP1 with RS and polydextrose could result in increased Wnt pathway activity. However, effects on Wnt pathway activity and downstream functional effects in the healthy large-bowel mucosa remain to be investigated. The DISC Study was registered at clinicaltrials.gov as NCT01214681.

Indexed as

Epigenesis, GeneticAdolescentAdultAgedAged, 80 and overDietary CarbohydratesDNA MethylationDouble-Blind MethodDown-RegulationFecesFemaleGlucansHumansIntercellular Signaling Peptides and ProteinsIntestinal MucosaLeukocyte L1 Antigen ComplexDietary CarbohydratesGlucansIntercellular Signaling Peptides and ProteinsLeukocyte L1 Antigen ComplexMembrane ProteinsMicroRNAspolydextroseRNA, MessengerSecreted Frizzled-Related ProteinsSFRP1 protein, humanStarchcalprotectincolorectal cancerepigeneticsnondigestible carbohydratesWnt signaling

Identifiers

PMID28077379
PMCPMC5267298
OpenAlexW2577073826

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.