Intake of up to 3 Eggs per Day Is Associated with Changes in HDL Function and Increased Plasma Antioxidants in Healthy,Young Adults123

HDL function may be more important than HDL concentration in determining risk for cardiovascular disease.In addition,HDL is a carrier of carotenoids and antioxidant enzymes,which protect HDL and LDL particles against oxidation. The goal of this study was to determine the impact of consuming 0–3 eggs/d on LDL and HDL particle size,HDL function,and plasma antioxidants in a young,healthy population. Thirty-eight healthy men and women [age 18–30 y,body mass index (in kg/m2) 18.5–29.9] participated in this 14-wk crossover intervention.Subjects underwent a 2-wk washout (0 eggs/d) followed by sequentially increasing intake of 1,2,and 3 eggs/d for 4 wk each.After each period,fasting blood was collected for analysis of lipoprotein subfractions,plasma apolipoprotein (apo) concentration,lutein and zeaxanthin concentration,and activities of lecithin-cholesterol acyltransferase,cholesteryl ester transfer protein,and paraoxonase-1. Compared with intake of 0 eggs/d,consuming 1–3 eggs/d resulted in increased large-LDL (21–37%) and large-HDL (6–13%) particle concentrations,plasma apoAI (9–15%),and lecithin-cholesterol acyltransferase activity (5–15%) (P< 0.05 for all biomarkers).Intake of 2–3 eggs/d also promoted an 11% increase in apoAII (P< 0.05) and a 20–31% increase in plasma lutein and zeaxanthin (P< 0.05),whereas intake of 3 eggs/d resulted in a 9–16% increase in serum paraoxonase-1 activity compared with intake of 1–2 eggs/d (P< 0.05).Egg intake did not affect cholesteryl ester transfer protein activity. Intake of 1 egg/d was sufficient to increase HDL function and large-LDL particle concentration; however,intake of 2–3 eggs/d supported greater improvements in HDL function as well as increased plasma carotenoids.Overall,intake of ≤3 eggs/d favored a less atherogenic LDL particle profile,improved HDL function,and increased plasma antioxidants in young,healthy adults.This trial was registered at clinicaltrials.gov as NCT02531958.