Evidence map›Paper›PMID 22715394›Full record

Trial reportPloS one2012

Selenium, selenoenzymes, oxidative stress and risk of neoplastic progression from Barrett's esophagus: results from biomarkers and genetic variants.

Yumie Takata, Alan R Kristal, Regina M Santella, Irena B King, David J Duggan, Johanna W Lampe, Margaret P Rayman, Patricia L Blount, Brian J Reid, Thomas L Vaughan and 1 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 22% 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

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

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Environmental Selenium and Human Health: an Update.Current environmental health reports · 2018
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Predictive biomarkers for Barrett's esophagus: so near and yet so far.Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus · 2013
    Review
  16. Article
  17. Review
  18. Article
  19. 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 2 countries.

Yumie TakataPublic Health Science Division, Fred Hutchinson Cancer Research Center, Seattle, Washington, United States of America.
Alan R Kristal
Regina M Santella
Irena B King
David J Duggan
Johanna W Lampe
Margaret P Rayman
Patricia L Blount
Brian J Reid
Thomas L Vaughan
Ulrike Peters
Fred Hutch Cancer Center · USColumbia University · USTranslational Genomics Research Institute · USUniversity of Surrey · GB

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Marian Esvelt · 1985 to 2026
$296.4M
PHYLOGENIES of Barrett's Esophagus LineagesP01CA091955 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GRADY, WILLIAM MALLORY · 2002 to 2019
$35.9M
Human Se Nutritional Requirement and Biomarkers in Health and DiseaseR01DK058763 · NIDDK · VANDERBILT UNIVERSITY · PI BURK, RAYMOND F. · 2001 to 2010
$3.6M
ESTABLISHED INVESTIGATOR AWARD IN CANCER PREVENTION AND CONTROLK05CA124911 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI VAUGHAN, THOMAS L · 2007 to 2016
$1.6M
Selenium genetic variation in selenoenzymes and prostate cancerK22CA118421 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETERS, ULRIKE · 2006 to 2008
$468k
NCI NIH HHS K05 CA124911NCI NIH HHS K05CA124911NCI NIH HHS K22 CA118421NCI NIH HHS P01 CA091955NCI NIH HHS P01 CA91955NCI NIH HHS P30 CA015704NIDDK NIH HHS DK58763NIDDK NIH HHS R01 DK058763
6 · The paper itself

Abstract

Clinical trials have suggested a protective effect of selenium supplementation on the risk of esophageal cancer, which may be mediated through the antioxidant activity of selenoenzymes. We investigated whether serum selenium concentrations, selenoenzyme activity, oxidative stress and genetic variation in selenoenzymes were associated with the risk of neoplastic progression to esophageal adenocarcinoma (EA) and two intermediate endpoints, aneuploidy and tetraploidy. In this prospective cohort study, during an average follow-up of 7.3 years, 47 EA cases, 41 aneuploidy cases and 51 tetraploidy cases accrued among 361 participants from the Seattle Barrett's Esophagus Research Study who were free of EA at the time of blood draw and had at least one follow-up visit. Development to EA was assessed histologically and aneuploidy and tetraploidy by DNA content flow cytometry. Serum selenium concentrations were measured using atomic absorption spectrometry, activity of glutathione peroxidase (GPX) 1 and GPX3 by substrate-specific coupled test procedures, selenoprotein P (SEPP1) concentrations and protein carbonyl content by ELISA method and malondialdehyde concentrations by HPLC. Genetic variants in GPX1-4 and SEPP1 were genotyped. Serum selenium was not associated with the risk of neoplastic progression to EA, aneuploidy or tetraploidy (P for trend = 0.25 to 0.85). SEPP1 concentrations were positively associated with the risk of EA [hazard ratio (HR) = 3.95, 95% confidence intervals (CI) = 1.42-10.97 comparing the third tertile with the first] and with aneuploidy (HR = 6.53, 95% CI = 1.31-32.58), but not selenoenzyme activity or oxidative stress markers. No genetic variants, overall, were associated with the risk of neoplastic progression to EA (global p = 0.12-0.69). Our results do not support a protective effect of selenium on risk of neoplastic progression to EA. Our study is the first to report positive associations of plasma SEPP1 concentrations with the risk of EA and aneuploidy, which warrants further investigation.

Indexed as

AdenocarcinomaAneuploidyBarrett EsophagusBiomarkers, TumorEsophageal NeoplasmsNeoplasm ProteinsAgedAged, 80 and overFemaleFollow-Up StudiesGlutathione PeroxidaseGlutathione Peroxidase GPX1HumansMaleMiddle AgedOxidative StressBiomarkers, TumorGlutathione PeroxidaseGlutathione Peroxidase GPX1GPX1 protein, humanGPX3 protein, humanNeoplasm ProteinsSeleniumSelenoproteins

Identifiers

PMID22715394
PMCPMC3371043
OpenAlexW2045986339

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.