Fatigue, inflammation, and ω-3 and ω-6 fatty acid intake among breast cancer survivors

J Clin Oncol. 2012 Apr 20;30(12):1280-7. doi: 10.1200/JCO.2011.36.4109. Epub 2012 Mar 12.

Abstract

Purpose: Evidence suggests that inflammation may drive fatigue in cancer survivors. Research in healthy populations has shown reduced inflammation with higher dietary intake of ω-3 polyunsaturated fatty acids (PUFAs), which could potentially reduce fatigue. This study investigated fatigue, inflammation, and intake of ω-3 and ω-6 PUFAs among breast cancer survivors.

Methods: Six hundred thirty-three survivors (mean age, 56 years; stage I to IIIA) participating in the Health, Eating, Activity, and Lifestyle Study completed a food frequency/dietary supplement questionnaire and provided a blood sample assayed for C-reactive protein (CRP) and serum amyloid A (30 months after diagnosis) and completed the Piper Fatigue Scale and Short Form-36 (SF-36) vitality scale (39 months after diagnosis). Analysis of covariance and logistic regression models tested relationships between inflammation and fatigue, inflammation and ω-3 and ω-6 PUFA intake, and PUFA intake and fatigue, controlling for three incremental levels of confounders. Fatigue was analyzed continuously (Piper scales) and dichotomously (SF-36 vitality ≤ 50).

Results: Behavioral (P = .003) and sensory (P = .001) fatigue scale scores were higher by increasing CRP tertile; relationships were attenuated after adjustment for medication use and comorbidity. Survivors with high CRP had 1.8 times greater odds of fatigue after full adjustment (P < .05). Higher intake of ω-6 relative to ω-3 PUFAs was associated with greater CRP (P = .01 after full adjustment) and greater odds of fatigue (odds ratio, 2.6 for the highest v lowest intake; P < .05).

Conclusion: Results link higher intake of ω-3 PUFAs, decreased inflammation, and decreased physical aspects of fatigue. Future studies should test whether ω-3 supplementation may reduce fatigue among significantly fatigued breast cancer survivors.

Publication types

  • Comparative Study
  • Multicenter Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Aged
  • Analysis of Variance
  • Breast Neoplasms / complications
  • Breast Neoplasms / pathology
  • Breast Neoplasms / therapy*
  • C-Reactive Protein / metabolism
  • Carcinoma, Intraductal, Noninfiltrating / complications
  • Carcinoma, Intraductal, Noninfiltrating / pathology
  • Carcinoma, Intraductal, Noninfiltrating / therapy
  • Cohort Studies
  • Dietary Supplements*
  • Fatigue / etiology
  • Fatigue / physiopathology
  • Fatigue / therapy*
  • Fatty Acids, Omega-3 / administration & dosage*
  • Fatty Acids, Omega-3 / blood
  • Fatty Acids, Omega-6 / administration & dosage*
  • Fatty Acids, Omega-6 / blood
  • Female
  • Follow-Up Studies
  • Humans
  • Inflammation / etiology
  • Inflammation / physiopathology
  • Inflammation / therapy*
  • Inflammation Mediators / analysis
  • Logistic Models
  • Middle Aged
  • Odds Ratio
  • Prospective Studies
  • Risk Assessment
  • Serum Amyloid A Protein / metabolism
  • Survivors
  • Treatment Outcome

Substances

  • Fatty Acids, Omega-3
  • Fatty Acids, Omega-6
  • Inflammation Mediators
  • Serum Amyloid A Protein
  • C-Reactive Protein