Evidence map›Paper›PMID 23233733›Full record

Trial reportCancer prevention research (Philadelphia, Pa.)2013

Prolonged biologically active colonic tissue levels of curcumin achieved after oral administration--a clinical pilot study including assessment of patient acceptability.

Glen R B Irving, Lynne M Howells, Stewart Sale, Ines Kralj-Hans, Wendy S Atkin, Susan K Clark, Robert G Britton, Donald J L Jones, Edwina N Scott, David P Berry and 5 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Cancer prevention research (Philadelphia, Pa.), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

52 citing papers in PubMed, 109 citations in OpenAlex.

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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

15 authors at 4 institutions in 2 countries.

Glen R B IrvingDepartment of Cancer Studies and Molecular Medicine, University of Leicester, United Kingdom.
Lynne M Howells
Stewart Sale
Ines Kralj-Hans
Wendy S Atkin
Susan K Clark
Robert G Britton
Donald J L Jones
Edwina N Scott
David P Berry
David Hemingway
Andrew S Miller
Karen Brown
Andreas J Gescher
William P Steward
Imperial College London · GBSt Mark's Hospital · GBSt. Mark's Hospital · USUniversity Hospitals of Leicester NHS Trust · GB

Funding

Cancer Research UK 13101Cancer Research UK A15575Cancer Research UK A6894Cancer Research UK A7255Cancer Research UK C325/A15575Cancer Research UK C325/A6691Cancer Research UK C325/A7255Department of Health
6 · The paper itself

Abstract

Curcumin, the main constituent of turmeric, is suspected to possess cancer chemopreventive properties. Pharmacokinetic and pharmacodynamic parameters have been reported, but few data exist describing whether methodologies are suitably robust for curcuminoid detection in colonic biopsy specimens. Information on the acceptability of prolonged administration of daily curcumin is not available. This is of vital importance to implement chemoprevention strategies. This study aimed to quantify levels of curcuminoids in colorectal mucosa of patients undergoing colorectal endoscopy or surgical resection and to obtain information on the acceptability and compliance with daily curcumin. Curcumin C3 complex (2.35 g) was administered to patients once daily for 14 days before endoscopic biopsy or colonic resection. Safety and tolerance were monitored. Analysis of curcuminoids in plasma, urine, and colonic mucosa was conducted by ultraperformance liquid chromatography (UPLC)-UV with characterization by liquid chromatography/tandem mass spectrometry (LC/MS-MS). Twenty-four of 26 patients commencing curcumin completed the course. Six patients reported mild gastrointestinal adverse events. Curcuminoids were detectable in nine of 24 plasma samples, 24 of 24 urine samples, and in the colonic mucosa of all 23 biopsied participants. Mean tissue levels were 48.4 μg/g (127.8 nmol/g) of parent curcuminoids. The major conjugate, curcumin glucuronide, was detectable in 29 of 35 biopsies. High levels of topical curcumin persisted in the mucosa for up to 40 hours postadministration. Sixteen participants (67%) stated that they would take curcumin long-term should it be of proven benefit. In summary, pharmacologically active levels of curcumin were recovered from colonic mucosa. The regimen used here seems safe, and patients support its use in long-term trials.

Indexed as

Patient Acceptance of Health CareAdministration, OralAdultAgedAged, 80 and overAntineoplastic Agents, PhytogenicBiological AvailabilityCarcinomaColonColorectal NeoplasmsCurcuminFemaleHumansIntestinal MucosaMaleMiddle AgedAntineoplastic Agents, PhytogenicCurcumin

Identifiers

PMID23233733
PMCPMC3566223
OpenAlexW2135731245

What OpenQuestion holds

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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.