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Department of Family and Preventive Medicine, University of California, San Diego, La Jolla, CA 92093-0901
3To whom correspondence and reprint requests should be addressed.
We investigated predictors of change in plasma carotenoids from
baseline to 3 y and examined plasma carotenoid concentrations at 1
and 3 y in response to a high vegetable diet. Participants were 56
women diagnosed with breast cancer and enrolled in a randomized
feasibility study for a trial examining the effect of a diet high in
vegetables and fruits on the risk of breast cancer recurrence.
Independent t test analysis revealed that the
intervention group had significantly higher vegetable and fruit
servings and fiber at 12 mo and significantly higher vegetable servings
at 36 mo compared with the control group (P < 0.05). Energy intake from fat was significantly lower in the
intervention group at 12 and 36 mo. The intervention group had
significantly higher consumption of ß-carotene,
-carotene, lutein
and ß-cryptoxanthin at 12 mo (P < 0.05).
ß-Carotene,
-carotene and lutein intakes also were significantly
higher at 36 mo (P < 0.05). At 36 mo, the
intervention group had significantly higher plasma concentrations of
-carotene and ß-carotene compared with the control group.
Repeated-measures ANOVA revealed that the intervention group had
significantly increased (P < 0.05 with Bonferroni
correction) plasma ß-carotene,
-carotene, lutein and lycopene
concentrations at 12 and 36 mo compared with baseline. Baseline
carotenoid concentrations were significantly inversely predictive
(P < 0.05) of plasma carotenoid change. In
addition, change in body mass index (BMI) and plasma cholesterol
concentrations were predictive of plasma carotenoid change from
baseline to 3 y. Results of this study demonstrate that change in
plasma carotenoid concentrations is associated with change in BMI,
change in plasma cholesterol and baseline carotenoid concentrations.
Plasma carotenoid response can be an indicator of long-term high
vegetable intake for women at risk of breast cancer recurrence.
KEY WORDS: carotenoids biomarkers humans breast cancer
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