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American Journal of Clinical Nutrition, Vol. 77, No. 1, 56-62, January 2003
© 2003 American Society for Clinical Nutrition


Original Research Communication

Iron status in association with cardiovascular disease risk in 3 controlled feeding studies1,2,3

Jessica L Derstine, Laura E Murray-Kolb, Shaomei Yu-Poth, Rebecca L Hargrove, Penny M Kris-Etherton and John L Beard

1 From the Department of Nutrition, The Pennsylvania State University, University Park.

Background: The role of body iron stores in free radical–induced peroxidation and cardiovascular disease risk has been debated, but controlled feeding studies using measurements of non-transferrin-bound iron (NTBI) and LDL oxidation have not been conducted.

Objective: We tested the hypothesis that NTBI and other measures of iron status do not affect oxidative susceptibility in healthy subjects with normal iron status.

Design: Plasma samples were analyzed from 77 healthy men and women aged 20–65 y who participated in 3 controlled feeding studies in which the type and amount of dietary fat were controlled. Iron status and in vitro LDL oxidation were assessed at baseline and at the end of each feeding period (4–8 wk).

Results: No significant relations were found between any measure of iron status (ferritin: 83 ± 8.9 µg/L; iron: 20.9 ± 5.4 µmol/L; TIBC: 74.4 ± 11.0 µmol/L; NTBI: 0.184 ± 0.15 µmol/L) and the in vitro measures of LDL oxidation (total dienes: 485 ± 55 µmol/mg LDL protein; lag time: 51.7 ± 15.9 min; and rate of oxidation: 25.4 ± 6.8 µmol dienes·min-1·g LDL protein-1). Equal-iron peanut butter–based diets were associated with higher plasma iron in men (22.4 ± 3.8 µmol/L) than was the olive oil diet (17.7 ± 4.5 µmol/L) (P = 0.02), but this slight elevation did not alter LDL oxidation.

Conclusions: Diet composition may affect plasma iron in men, but LDL oxidative susceptibility is unaffected by the subtle variation in iron status. Thus, the results do not support a relation between iron status and LDL oxidative susceptibility, a possible risk factor for cardiovascular disease.

Key Words: Cardiovascular disease • iron • ferritin • total-iron-binding capacity • TIBC • conjugated dienes • lag time • lipids • LDL oxidation




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