Skip to main content
  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

  • Register
  • Log in
  • My Cart
Advertisement

Main menu

  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CEBP Focus Archive
    • Meeting Abstracts
    • Collections
      • Disparities Collection
      • Editors' Picks
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • OnlineFirst
    • Editors' Picks
    • Citation
    • Author/Keyword
  • News
    • Cancer Discovery News
  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

User menu

  • Register
  • Log in
  • My Cart

Search

  • Advanced search
Cancer Epidemiology, Biomarkers & Prevention
Cancer Epidemiology, Biomarkers & Prevention

Advanced Search

  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CEBP Focus Archive
    • Meeting Abstracts
    • Collections
      • Disparities Collection
      • Editors' Picks
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • OnlineFirst
    • Editors' Picks
    • Citation
    • Author/Keyword
  • News
    • Cancer Discovery News
Null Results in Brief

No Association between Fatty Acid Intake and Adenomatous Polyp Recurrence in the Polyp Prevention Trial

Marie M. Cantwell, Michele R. Forman, Paul S. Albert, Kirk Snyder, Arthur Schatzkin, Elaine Lanza and and The Polyp Prevention Trial Study Group
Marie M. Cantwell
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Michele R. Forman
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Paul S. Albert
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kirk Snyder
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Arthur Schatzkin
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Elaine Lanza
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI: 10.1158/1055-9965.EPI-05-0165 Published August 2005
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading
  • Diet, alcohol, smoking, and other lifestyle risk factors
  • Gastrointestinal cancers: colorectal

Introduction

Dietary fat intake and cancer risk have been investigated in detail in many populations, although the results have been inconsistent for colorectal cancer. Several molecular mechanisms have been proposed to explain how specific dietary fatty acids could alter colorectal cancer risk due to their involvement in varying physiologic functions (1). These include apoptosis, inflammation, cell proliferation, metastasis, gene expression, signal transduction, altered estrogen metabolism, free radical production, and mechanisms related to insulin sensitivity. Most previous studies have examined the association for total fat intake, fat from animal sources, or intake of the major classes of fat (saturated, monounsaturated or polyunsaturated fat) on colorectal cancer risk. The aim of the current study was to assess the association between intake of specific fatty acids and adenoma recurrence to obtain a better understanding of the role of dietary fat and colorectal cancer risk. The fatty acids hypothesized to have an association a priori were the fish fatty acids (eicosapentanoic and docosahexanoic acid), linolenic acid, arachidonic acid, the n3:n6 ratio, saturated fat, and total fat intake.

Patients and Methods

Study Population

The Polyp Prevention Trial was a large multicenter, randomized, controlled trial of the effect of a low fat, high-fiber, high-fruit and -vegetable dietary intervention on the recurrence of large bowel adenomas. This study has been previously described in detail (2, 3). Briefly, subjects were ≥35 years and had one or more histologically confirmed adenomas removed during a colonoscopy done within 6 months of randomization. Study participants had no history of colorectal cancer, bowel resection, surgical resection of adenomas, polyposis syndrome, or inflammatory bowel disease. The Polyp Prevention Trial included 2,079 participants who were randomly assigned to either the intervention diet (n = 1,037) that was low in fat and high in fiber, fruit, and vegetables, or to the control group (n = 1,042) and followed their usual diet for 4 years.

Dietary Assessment

All participants (control and intervention) completed a 4-day food record at baseline (T0) and in conjunction with annual visits at the end of years 1, 2, 3, and 4. Trained, certified nutritionists reviewed all completed 4-day food records with the participants (2). A 20% sample of the 4-day food records were identified randomly with stratification by clinical center and were coded and analyzed immediately. The current analysis presents results from 372 participants who completed 4-day food records at all four time points, 181 were randomized to the intervention group and 191 to the control group.

Statistical Analysis

Odds ratios and 95% confidence intervals were estimated using logistic regression models with adenoma recurrence as the end point. Fatty acid intake (g/1,000 kcal) was treated categorically in tertiles and regression models were adjusted for age (continuous), gender (male/female), group (intervention/control), baseline nonsteroidal anti-inflammatory drug use (yes/no), body mass index (continuous), family history of colorectal cancer (yes/no), and an interaction term for group × gender. Tests for trend were done using the scores derived from the median of each tertile of fatty acid intake. Stratification of the models by group (intervention/control) did not alter the results. In addition, models without adjustments for group showed similar results.

Results and Discussion

Total fat intake at baseline and the average intake over the 4-year interval were not statistically significantly associated with adenoma recurrence. Total fat and individual fatty acid intakes were similar to those in previous studies that have examined the association with colorectal adenoma recurrence. Increasing total fat and saturated fat intake, calculated as the average of years 1, 2, and 3 (T1-T3), were not associated with a statistically significant increase in the odds of recurrence. Although a previous analysis (4) of a larger cohort from the Polyp Prevention Trial found a statistically significant decrease in risk of multiple adenomas and fish intake assessed by a food frequency questionnaire, we found no association of fish fatty acid intake (eicosapentaenoic acid plus docosahexanoic acid; T1-T3) and odds of recurrence. These results remained the same when the analysis was repeated for those with an end point of multiple adenomas. Although the average of four 4-day food records was used to assess dietary intake in this population, it should be noted that it is particularly challenging to assess fatty acid intake. Food composition databases may not accurately reflect the individual fatty acid content as the composition varies between brands and over time depending on the type of oil used to manufacture spreads and processed foods which may vary due to availability and production costs (5). A large variability in the n-3 fatty acid content between different species of fish adds to the complexity of assessing intake accurately. In addition, the presence of endogenously produced fatty acids and differences in fatty acid metabolism as well as other lifestyle factors increase the complexity of this relationship. Finally, it is possible that this study failed to observe a statistically significant association due to the small sample size. We did a Monte-Carlo study with 2,000 simulated data sets to evaluate the power to detect meaningful associations between the biomarkers and adenoma recurrence. Calculations were based on a sample size of n = 372 (an equal number in each of the three tertiles) and an assumed 30% recurrence in the lower tertile. With these assumptions, we would have 87% power to detect an odds ratio of 1.50 and 2.25 for the second and third tertiles, respectively, using a two-sided trend test conducted at the 0.05 significance level. Thus, with our sample size, we can be assured that there are no substantial trends (Table 1).

View this table:
  • View inline
  • View popup
Table 1.

Association among tertiles of total fat intake, total saturated fatty acid, total fish fatty acids, arachidonic acid, linolenic acid, and the n3:n6 ratio assessed using 4-day food diaries and recurrence of large bowel adenomas in the Polyp Prevention Trial (n= 372)

We anticipated that the 4-day food records, which would assess the amount and type of fat/oil used in food preparation and the specific type of oily fish eaten, would capture usual fatty acid intake as well as total and saturated fatty acid intake. We hypothesized that differences in intake of specific fatty acids would increase or decrease risk of adenoma recurrence, as underlying mechanisms regarding the possible role of specific fatty acids and colorectal cancer have been proposed (1, 6). However, our findings do not support this hypothesis.

Footnotes

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

    • Accepted June 14, 2005.
    • Received March 14, 2005.
    • Revision received May 4, 2005.

References

  1. ↵
    Nkondjock A, Shatenstein B, Maisonneuve P, Ghadirian P. Specific fatty acids and human colorectal cancer: an overview. Cancer Detect Prev 2003;27:55–66.
    OpenUrlCrossRefPubMed
  2. ↵
    Lanza E, Schatzkin A, Daston C, et al. Implementation of a 4-y, high-fiber, high-fruit-and-vegetable, low-fat dietary intervention: results of dietary changes in the Polyp Prevention Trial. Am J Clin Nutr 2001;74:387–401.
    OpenUrlAbstract/FREE Full Text
  3. ↵
    Schatzkin A, Lanza E, Freedman LS, et al. The polyp prevention trial I: rationale, design, recruitment, and baseline participant characteristics. Cancer Epidemiol Biomarkers Prev 1996;5:375–83.
    OpenUrlAbstract/FREE Full Text
  4. ↵
    Mathew A, Sinha R, Burt R, et al. Eur J Cancer Prev 2004;13:159–64.
    OpenUrlCrossRefPubMed
  5. ↵
    Cantwell MM. Assessment of individual fatty acid intake. Proc Nutr Soc 2000;59:187–91.
    OpenUrlPubMed
  6. ↵
    Nkondjock A, Shatenstein B, Maisonneuve P, Ghadirian P. Assessment of risk associated with specific fatty acids and colorectal cancer among French-Canadians in Montreal: a case-control study. Int J Epidemiol 2003;32:200–9.
    OpenUrlAbstract/FREE Full Text
PreviousNext
Back to top
Cancer Epidemiology Biomarkers & Prevention: 14 (8)
August 2005
Volume 14, Issue 8
  • Table of Contents

Sign up for alerts

View this article with LENS

Open full page PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for sharing this Cancer Epidemiology, Biomarkers & Prevention article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
No Association between Fatty Acid Intake and Adenomatous Polyp Recurrence in the Polyp Prevention Trial
(Your Name) has forwarded a page to you from Cancer Epidemiology, Biomarkers & Prevention
(Your Name) thought you would be interested in this article in Cancer Epidemiology, Biomarkers & Prevention.
Citation Tools
No Association between Fatty Acid Intake and Adenomatous Polyp Recurrence in the Polyp Prevention Trial
Marie M. Cantwell, Michele R. Forman, Paul S. Albert, Kirk Snyder, Arthur Schatzkin, Elaine Lanza and and The Polyp Prevention Trial Study Group
Cancer Epidemiol Biomarkers Prev August 1 2005 (14) (8) 2059-2060; DOI: 10.1158/1055-9965.EPI-05-0165

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
No Association between Fatty Acid Intake and Adenomatous Polyp Recurrence in the Polyp Prevention Trial
Marie M. Cantwell, Michele R. Forman, Paul S. Albert, Kirk Snyder, Arthur Schatzkin, Elaine Lanza and and The Polyp Prevention Trial Study Group
Cancer Epidemiol Biomarkers Prev August 1 2005 (14) (8) 2059-2060; DOI: 10.1158/1055-9965.EPI-05-0165
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Introduction
    • Patients and Methods
    • Results and Discussion
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
Advertisement

Related Articles

Cited By...

More in this TOC Section

  • Psychotropic Medications and Breast Cancer
  • Genetic Variants and Colorectal Cancer Survival
  • Statin Use and Prostate Cancer Incidence in Manitoba, Canada
Show more Null Results in Brief
  • Home
  • Alerts
  • Feedback
  • Privacy Policy
Facebook   Twitter   LinkedIn   YouTube   RSS

Articles

  • Online First
  • Current Issue
  • Past Issues

Info for

  • Authors
  • Subscribers
  • Advertisers
  • Librarians
  • Reviewers

About Cancer Epidemiology, Biomarkers & Prevention

  • About the Journal
  • Editorial Board
  • Permissions
  • Submit a Manuscript
AACR logo

Copyright © 2019 by the American Association for Cancer Research.

Cancer Epidemiology, Biomarkers & Prevention
eISSN: 1538-7755
ISSN: 1055-9965

Advertisement