Abstract

BackgroundDietary phytosterols, plant sterols structurally similar to cholesterol, reduce intestinal cholesterol absorption and have many other potentially beneficial biological effects in humans. Due to limited information on phytosterol levels in foods, however, it is difficult to quantify habitual dietary phytosterol intake (DPI). Therefore, we sought to identify a plasma biomarker of DPI.Methods and FindingsData were analyzed from two feeding studies with a total of 38 subjects during 94 dietary periods. DPI was carefully controlled at low, intermediate, and high levels. Plasma levels of phytosterols and cholesterol metabolites were assessed at the end of each diet period. Based on simple ordinary least squares regression analysis, the best biomarker for DPI was the ratio of plasma campesterol to the endogenous cholesterol metabolite 5-α-cholestanol (R2 = 0.785, P < 0.0001). Plasma campesterol and 5-α-cholestanol levels varied greatly among subjects at the same DPI level, but were positively correlated at each DPI level in both studies (r > 0.600; P < 0.01).ConclusionThe ratio of plasma campesterol to the coordinately regulated endogenous cholesterol metabolite 5-α-cholestanol is a biomarker of dietary phytosterol intake. Conversely, plasma phytosterol levels alone are not ideal biomarkers of DPI because they are confounded by large inter-individual variation in absorption and turnover of non-cholesterol sterols. Further work is needed to assess the relation between non-cholesterol sterol metabolism and associated cholesterol transport in the genesis of coronary heart disease.

Highlights

  • In addition to their robust effects on cholesterol metabolism [1,2,3], phytosterols are reported to have many other biological actions, such as anti-inflammatory and anti-cancer effects [4,5]

  • Plasma phytosterol levels alone are not ideal biomarkers of dietary phytosterol intake (DPI) because they are confounded by large inter-individual variation in absorption and turnover of non-cholesterol sterols

  • Increasing phytosterol intake results in a plateau in plasma phytosterol levels, indicating competition of phytosterols for their own absorption [11,12]. These results suggest that plasma phytosterol levels are dependent on DPI, and on the absorption efficiency and the re-excretion rate of absorbed phytosterols

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Summary

Introduction

In addition to their robust effects on cholesterol metabolism [1,2,3], phytosterols are reported to have many other biological actions, such as anti-inflammatory and anti-cancer effects [4,5]. It is difficult to quantify habitual dietary phytosterol intake (DPI) because phytosterol levels in foods are not systematically included in food databases. A suitable plasma biomarker for DPI would be helpful in assessing the biological effects of dietary phytosterols in epidemiological studies. Many diet-related investigations rely on measurement of plasma levels of the nutrient being studied (phytosterols in this case) in order to estimate habitual dietary intake. Increasing phytosterol intake results in a plateau in plasma phytosterol levels, indicating competition of phytosterols for their own absorption [11,12]. Due to limited information on phytosterol levels in foods, it is difficult to quantify habitual dietary phytosterol intake (DPI). We sought to identify a plasma biomarker of DPI

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