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 = (-)
- RE = (-)
- 1 PC, G. Tom intake as part of food intake pattern (5 y follow up)
- RE = (+) on PAI-1 and fibrinogen
- RE = (+) on PAI-1 and fibrinogen
- CHD subjects: n=30
- 1 Interv, P.Tom
- RE = (-)
38
- 1 Interv, P.Tom
- Periodontal Disease subjects: n=? cases
- 1 PC, G. Tom and Lyco
- RE = (-)
- 1 PC, G. Tom and Lyco
- Renal Transplant subjects: n=15
- 1 Interv, P.Tom
- RE = N
- 1 Interv, P.Tom
- 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.
- 9 studies n= ≤ 17 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
- 3 studies n= 10, n=10 and n=64 subjects (non-disease) - Ox
- 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.
- Varied between single dose/1 day (1 study) to 2 months (1 study).


