0
Letters |

Selenium and Vitamin E Supplementation for Cancer Prevention

Margaret P. Rayman, DPhil; Gerald F. Combs, PhD; David J. Waters, PhD, DVM
JAMA. 2009;301(18):1876-1877. doi:10.1001/jama.2009.625
Text Size: A A A
Published online

To the Editor: The Selenium and Vitamin E Cancer Prevention Trial (SELECT) by Dr Lippman and colleagues1 reported that selenium or vitamin E alone or in combination did not prevent prostate cancer. The negative results of this trial confirm the outcomes in the Nutritional Prevention of Cancer (NPC) Trial for those participants with the highest baseline plasma selenium concentration prior to supplementation with selenized yeast.2 The conclusion from both NPC and SELECT should be that daily selenium supplementation will not benefit all persons. Cancer risk reduction with selenium should be expected only in men with low or suboptimal levels prior to supplementation.

A U-shaped dose-response relationship between selenium intake and cancer risk, as suggested by studies in dogs,3 is consistent with the results of SELECT and NPC. At baseline, the average participant in SELECT had selenium status within the trough of the U-shaped curve, ie, not low or suboptimal. After supplementation with 200 μg per day of selenium as selenomethionine, the average SELECT participant achieved selenium levels that far exceeded the high postsupplementation values of men in NPC in the highest baseline-selenium tertile. Those NPC participants experienced no prostate-cancer risk reduction and an almost 3-fold increased incidence of diabetes.2 ,4 In SELECT, there was no reduction in prostate-cancer risk and a statistically nonsignificant increased diabetes incidence. We therefore consider the results of SELECT and NPC to be consistent, not contradictory.

We believe that it is time to move beyond the belief that any particular agent administered at the same dose to all participants will benefit the overall population and instead attempt to individualize cancer prevention.3 Subsets of individuals should be identified who are more likely to benefit from supplementation, such as persons with low selenium concentrations or perhaps those with the selenoprotein-P genotype that is associated with prostate-cancer risk.5 This stance is distinct from claiming knowledge of which types of cancer will or will not be prevented by selenium.

AUTHOR INFORMATION

Financial Disclosures: Dr Rayman reported receiving grant support from Wassen International, a manufacturer of nutritional supplements, including selenium. Dr Waters reported that he is director of the Murphy Cancer Foundation, a not-for-profit research institute that, in collaboration with Bostwick Laboratories, markets a toenail test for selenium. Dr Waters reported that he has no financial interest in Bostwick Laboratories and no financial relationships with any manufacturers of selenium supplements. Dr Combs reported no disclosures.

REFERENCES

Lippman SM, Klein EA, Goodman PJ,  et al.  Effect of selenium and vitamin E on risk of prostate cancer and other cancers: the Selenium and Vitamin E Cancer Prevention Trial (SELECT).  JAMA. 2009;301(1):39-51
PubMedCrossRef
Duffield-Lillico AJ, Reid ME, Turnbull BW,  et al.  Baseline characteristics and the effect of selenium supplementation on cancer incidence in a randomized clinical trial: a summary report of the Nutritional Prevention of Cancer Trial.  Cancer Epidemiol Biomarkers Prev. 2002;11(7):630-639
PubMed
Waters DJ, Chiang EC, Bostwick DG. The art of casting nets: fishing for the prize of personalized cancer prevention.  Nutr Cancer. 2008;60(1):1-6
PubMedCrossRef
Stranges S, Marshall JR, Natarajan R,  et al.  Effects of long-term selenium supplementation on the incidence of type 2 diabetes: a randomized trial.  Ann Intern Med. 2007;147(4):217-223
PubMed
Cooper ML, Adami HO, Grönberg H, Wiklund F, Green FR, Rayman MP. Interaction between single nucleotide polymorphisms in selenoprotein P and mitochondrial superoxide dismutase determines prostate cancer risk.  Cancer Res. 2008;68(24):10171-10177
PubMedCrossRef

First Page Preview

First page PDF preview

Figures

Tables

Interactive Graphics

Video

Country-Specific Mortality and Growth Failure in Infancy and Yound Children and Association With Material Stature

Use interactive graphics and maps to view and sort country-specific infant and early dhildhood mortality and growth failure data and their association with maternal

Lippman SM, Klein EA, Goodman PJ,  et al.  Effect of selenium and vitamin E on risk of prostate cancer and other cancers: the Selenium and Vitamin E Cancer Prevention Trial (SELECT).  JAMA. 2009;301(1):39-51
PubMedCrossRef
Duffield-Lillico AJ, Reid ME, Turnbull BW,  et al.  Baseline characteristics and the effect of selenium supplementation on cancer incidence in a randomized clinical trial: a summary report of the Nutritional Prevention of Cancer Trial.  Cancer Epidemiol Biomarkers Prev. 2002;11(7):630-639
PubMed
Waters DJ, Chiang EC, Bostwick DG. The art of casting nets: fishing for the prize of personalized cancer prevention.  Nutr Cancer. 2008;60(1):1-6
PubMedCrossRef
Stranges S, Marshall JR, Natarajan R,  et al.  Effects of long-term selenium supplementation on the incidence of type 2 diabetes: a randomized trial.  Ann Intern Med. 2007;147(4):217-223
PubMed
Cooper ML, Adami HO, Grönberg H, Wiklund F, Green FR, Rayman MP. Interaction between single nucleotide polymorphisms in selenoprotein P and mitochondrial superoxide dismutase determines prostate cancer risk.  Cancer Res. 2008;68(24):10171-10177
PubMedCrossRef
May 13, 2009
Rachel Hurst, PhD; Susan Fairweather-Tait, PhD
JAMA. 2009;301(18):1876-1877.
May 13, 2009
Scott M. Lippman, MD; Eric A. Klein, MD; Phyllis J. Goodman, MS
JAMA. 2009;301(18):1876-1877.
CME Course for:


You need to register in order to view this quiz.


To understand the clinical management of acute heart failure syndromes.
Accreditation Information The American Medical Association is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.
The AMA designates this journal-based CME activity for a maximum of 1 AMA PRA Category 1 CreditTM per course. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Physicians who complete the CME course and score at least 80% correct on the quiz are eligible for AMA PRA Category 1 CreditTM.
Note: You must get at least of the answers correct to pass this quiz.
Note: You must get at least of the answers correct to pass this quiz.
You have not filled in all the answers to complete this quiz
The following questions were not answered:
Sorry, you have unsuccessfully completed this CME quiz with a score of
The following questions were not answered correctly:
For CME Course: A Proposed Model for Initial Assessment and Management of Acute Heart Failure Syndromes
Indicate what changes(s) you will implement in your practice, if any, based on this CME course.
To view and print your certificate and access a summary of your CME courses go to My CME.
NOTE:
Citing articles are presented as examples only. In non-demo SCM6 implementation, integration with CrossRef’s “Cited By” API will populate this tab (http://www.crossref.org/citedby.html).
Submit a Response

Some tools below are only available to our subscribers or users with an online account.

Related Content

Customize your page view by dragging & repositioning the boxes below.