Milk polar lipids reduce lipid cardiovascular risk factors in overweight postmenopausal women: towards a gut sphingomyelin-cholesterol interplay

内科学 内分泌学 胆固醇 肠道菌群 脂质代谢 交叉研究 鞘磷脂 生物 医学 生物化学 安慰剂 病理 替代医学
作者
Cécile Vors,Laurie Joumard‐Cubizolles,Manon Lecomte,Emmanuel Combe,Lemlih Ouchchane,Jocelyne Drai,Ketsia Raynal,Florent Joffre,Laure Meiller,Mélanie Le Barz,Patrice Gaborit,A. Caillé,Monique Sothier,Carla Domingues-Faria,Adeline Blot,Aurélie Wauquier,Emilie Blond,Valérie Sauvinet,Geneviève Gésan-Guiziou,Jean-Pierre Bodin,Philippe Moulin,David Cheillan,Hubert Vidal,Béatrice Morio,Eddy Cotte,Françoise Morel-Laporte,M. Laville,Annick Bernalier‐Donadille,S. Lambert-Porcheron,Corinne Malpuech‐Brugère,Marie‐Caroline Michalski
出处
期刊:Gut [BMJ]
卷期号:69 (3): 487-501 被引量:97
标识
DOI:10.1136/gutjnl-2018-318155
摘要

Objective To investigate whether milk polar lipids (PL) impact human intestinal lipid absorption, metabolism, microbiota and associated markers of cardiometabolic health. Design A double-blind, randomised controlled 4-week study involving 58 postmenopausal women was used to assess the chronic effects of milk PL consumption (0, 3 or 5 g-PL/day) on lipid metabolism and gut microbiota. The acute effects of milk PL on intestinal absorption and metabolism of cholesterol were assessed in a randomised controlled crossover study using tracers in ileostomy patients. Results Over 4 weeks, milk PL significantly reduced fasting and postprandial plasma concentrations of cholesterol and surrogate lipid markers of cardiovascular disease risk, including total/high-density lipoprotein-cholesterol and apolipoprotein (Apo)B/ApoA1 ratios. The highest PL dose preferentially induced a decreased number of intestine-derived chylomicron particles. Also, milk PL increased faecal loss of coprostanol, a gut-derived metabolite of cholesterol, but major bacterial populations and faecal short-chain fatty acids were not affected by milk PL, regardless of the dose. Acute ingestion of milk PL by ileostomy patients shows that milk PL decreased cholesterol absorption and increased cholesterol-ileal efflux, which can be explained by the observed co-excretion with milk sphingomyelin in the gut. Conclusion The present data demonstrate for the first time in humans that milk PL can improve the cardiometabolic health by decreasing several lipid cardiovascular markers, notably through a reduced intestinal cholesterol absorption involving specific interactions in the gut, without disturbing the major bacterial phyla of gut microbiota. Trial registration number NCT02099032 and NCT02146339 ; Results.
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