Phosphorus supplement alters postprandial lipemia of healthy male subjects: A pilot cross-over trial

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BioMed Central Ltd.

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Background: Epidemiological studies have found a U-shaped relationship between serum phosphorus and cardiovascular disease (CVD). The mechanism(s) behind such a relationship are poorly understood. Phosphorus (P) is reported to improve insulin sensitivity, which is involved in lipid metabolism, and thus we were interested in determining the impact of phosphorus ingestion on postprandial lipemia, a recognized CVD risk factor. Findings. A within-subject study design was conducted, whereby 8 healthy male subjects received a high fat meal (330Kcal; 69% energy from fat; 35 mg of phosphorus) with placebo or phosphorus (500 mg) in a random order. Postprandial blood samples (∼10 ml) were collected every hour for 6 hours after meal ingestion. Changes in different parameters were analyzed using a 2-factor repeated-measure ANOVA. In the phosphorus (P) supplemented group, postprandial serum P increased (p = 0.00), while changes in insulin, non-esterified fatty acids (NEFA) and triglyceride (TG) were not significantly different than that of placebo. Concurrently, phosphorus supplementation increased postprandial concentrations of apolipoprotein B48 (ApoB48) (p < 0.05) and decreased that of apolipoprotein B100 (ApoB100) (p < 0.05). Conclusions: Phosphorus supplementation (500 mg) of the meal seems to alter the different components of postprandial lipemia. These findings highlight the potential role of phosphorus in CVD. © 2014 Hazim et al.; licensee BioMed Central Ltd.

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Apob100, Apob48, Lipids, Lipoproteins, Phosphorus, Postprandial lipemia, Administration, oral, Apolipoprotein b-100, Apolipoprotein b-48, Cross-over studies, Dietary supplements, Fatty acids, nonesterified, Healthy volunteers, Humans, Insulin, Lipid metabolism, Male, Pilot projects, Postprandial period, Triglycerides, Young adult, Apolipoprotein b100, Apolipoprotein b48, Fatty acid, Triacylglycerol, Blood, Controlled study, Crossover procedure, Diet supplementation, Drug effects, Human, Normal human, Oral drug administration, Pilot study, Postprandial state, Randomized controlled trial

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