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© 2003 The American Society for Nutritional Sciences J. Nutr. 133:1930-1936, June 2003


Nutritional Epidemiology

Variations in Plasma Lycopene and Specific Isomers over Time in a Cohort of U.S. Men

Kana Wu*,2, Steven J. Schwartz{dagger}, Elizabeth A. Platz**, Steven K. Clinton{ddagger}, John W. Erdman, Jr.{dagger}{dagger}, Mario G. Ferruzzi{dagger}, Walter C. Willett*,{ddagger}{ddagger},# and Edward L. Giovannucci*,{ddagger}{ddagger},#

* Department of Nutrition, Harvard School of Public Health, Boston, MA; {dagger} Department of Food Science and Technology, The Ohio State University, Columbus, OH; ** Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; {ddagger} Division of Hematology and Oncology, Department of Internal Medicine and Comprehensive Cancer Center, The Ohio State University, Columbus, OH; {dagger}{dagger} Division of Nutritional Sciences, University of Illinois, Urbana, IL; {ddagger}{ddagger} Department of Epidemiology, Harvard School of Public Health, Boston, MA; and # Channing Laboratory, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA

2To whom correspondence should be addressed. E-mail: kana.wu{at}channing.harvard.edu.

Epidemiologic and laboratory studies suggest a possible role for tomato products, a rich source of the carotenoid lycopene, in the prevention of certain cancers and cardiovascular disease. Lycopene is consumed primarily as the all-trans-isomer, but the majority of lycopene in blood and tissue exists as a variety of cis-isomers. Specific isomers may be involved in different biological reactions, and patterns of isomers may provide insight into the risk or pathogenesis of disease processes. Total lycopene concentration and the concentrations of the cis- and trans-lycopene isomers were measured by HPLC in plasma samples taken 3–4 y apart from 144 mostly nonsmoking male participants in the Health Professionals Follow-up Study. Correlations between plasma concentrations determined 3–4 y apart ranged from 0.55 (all-trans-isomer) to 0.70 (cis-isomer 5 -cis) (P < 0.001). For total lycopene, the correlation was 0.63 (P < 0.001). Total cis-lycopene contributed ~67% of total lycopene (range 50–79%). At each time point, the various lycopene isomer concentrations were highly correlated with one another with Spearman correlation coefficients ranging from 0.90 to 0.99 (P < 0.001). Plasma concentrations of total lycopene and its most abundant isomers in samples taken 3–4 y apart were strongly correlated, indicating that dietary patterns and metabolic processes defining lycopene concentrations are stable over time. Because the patterns of lycopene isomers showed limited between-person variability, our results suggest that measuring specific lycopene isomers in epidemiologic studies may not provide additional information beyond that provided by total lycopene concentration. Single plasma samples quantitating plasma lycopene are a valid predictor of long-term exposure for epidemiologic studies.


KEY WORDS: • lycopene • isomers • reproducibility




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