Cardiovascular Disease (CVD) - Tomato/Tomato-based foods and Disease Risk

Main findings

  • The data suggest a protective relationship between the intake of tomato/tomatobased foods and CVD through its effects on oxidative stress endpoints (e.g. LDL
    oxidation susceptibility).
  • Recent updates include information on the relationship between tomatoes/tomatobased foods and inflammation endpoints. However, data are inconclusive.
  • One PC study suggests increased vascular risk with tomatoes/tomato-based foods measured by pro-thrombotic factors in the blood. These data require follow up.

Summary of studies and outcomes

  • Number of studies = 32
  • Risk estimates (RE) = 43
    • (-) = 28
    • N = 14
    • (+) = 1
  • Risk estimates by Tomato or Lycopene category
    • √GT G. Tom = 11 (-), 6 (N), 1 (+)
    • √PT P. Tom = 15 (-), 7 (N)
    • √FT F. Tom = 1 (-)
    • √Lyco Lyco = 1 (-), 1 (N)


Summary Considerations/Notes:

  • Studies varied in type with the greatest representation by intervention (baseline control/ no placebo) studies.
  • Five (6) of 32 studies utilized subjects with existing disease.
  • DM subjects (3 studies): n=57, n=40, and 144 cases in cohort of 880, respectively.
    1 RCT, P.Tom, ~14/txt group
    • RE = (-)/N
  • 1 Interv, G.Tom
    • RE = (-)
  • 1 PC, G. Tom intake as part of food intake pattern (5 y follow up)
    • RE = (+) on PAI-1 and fibrinogen
  • CHD subjects: n=30
    • 1 Interv, P.Tom
    • RE = (-)
      38
  • Periodontal Disease subjects: n=? cases
    • 1 PC, G. Tom and Lyco
    • RE = (-)
  • Renal Transplant subjects: n=15
    • 1 Interv, P.Tom
    • RE = N
  • Sample size considerations:
  • Of the 15 intervention studies investigating effects of tomato/tomato-based foods on oxidative stress endpoints;
    • 9 studies n= ≤ 17 subjects,
    • 2 studies n= 20-23 subjects,
    • 3 studies n= 30-40 subjects and,
    • 1 study, n= 60 subjects.
  • Of the 10 RCTs investigating effects of tomato/tomato-based foods on oxidative stress, inflammation and or endothelial function endpoints;
    • 3 studies n= 10, n=10 and n=64 subjects (non-disease) - Ox
    • 4 studies n=103, n= 22, n=22 and n=22 subjects (non-disease) – Ox, inflammation, endothelial function (n=22 may be the same subj pop)
    • 1 study n= 39 subjects (smokers) - Ox
    • 1 study n= 57, ~14/treatment group (DM subjects) – Ox
    • 1 study n= 24 subjects – TC and CRP
  • Study duration:
    • Varied between single dose/1 day (1 study) to 2 months (1 study).
    • Typical study duration for intervention and RCT studies was 2-3 weeks with a 1-2 week run-in preceding intervention.