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临床试验/NCT05235464
NCT05235464招募中不适用

Dissecting the Impact of Dietary Protein on Macrophage mTOR Signaling and Atherosclerosis

University of Missouri-Columbia2 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2023年3月13日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
24
试验地点
2
主要终点
Monocyte p-S6 content

研究概览

简要总结

Atherosclerosis is the underlying cause of the majority of cardiovascular diseases, including myocardial infarction and strokes, and results in tremendous morbidity and mortality. A Western-type diet is a major risk factor for atherosclerosis because of the high saturated fat, cholesterol, and refined carbohydrate contents. Dietary strategies to reduce cardiovascular disease burden therefore focus on restriction of saturated fat, cholesterol, and refined carbohydrates whereas "lean" protein intake is recommended and has become popular. However, results from studies conducted in animal models suggest high dietary protein intake is also atherogenic. The investigators' extensive preliminary data in animal models show that dietary protein increases atherosclerotic plaque formation and size and promotes necrotic core formation, a characteristic of rupture-prone plaques. The goal of the current proposal is to provide deeper insights into the relationship between protein intake and the pathogenesis of atherosclerosis by studying the mechanisms involved in protein-mediated atherogenesis and formation of necrotic plaques. The overarching hypothesis is that high protein intake drives atherosclerosis via leucine-mediated mTORC1 signaling in macrophages, which inhibits macrophage mitophagy and aggrephagy and stimulates macrophage proliferation. Furthermore, the investigators hypothesize that proteins from animal sources are more atherogenic than proteins from plant sources, because animal proteins contain more leucine than plant proteins. The investigators will test these hypotheses by using a sophisticated array of experimental strategies, including assays in primary macrophages and human monocyte-derived macrophages and genetically engineered mouse models. In addition, they will begin to translate the results obtained in vitro and in animals to people, and explore approaches to pharmacologically target the pro-atherogenic pathways as novel cardiovascular therapeutics. This proposal represents a paradigm shift in how a Western-type diet affects vascular health which has important implications since many adults in Western societies consume excess protein and dietary protein is heavily marketed for its presumed beneficial health effects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • >=45 and <=75 years of age
  • body mass index >=25.0 and <40.0 kg/m2

排除标准

  • <45 and >75 years of age
  • body mass index <25.0 or >39.9 kg/m2
  • plasma triglyceride <125 mg/dl
  • history of or current significant organ system dysfunction
  • allergies or intolerances to meal ingredients
  • use of medications or dietary supplements that could confound the study outcomes
  • engaged in regular structured exercise >150 min per week
  • alcohol use disorder
  • premenopausal women
  • persons who smoke
  • prisoners
  • inability to grant voluntary informed consent

研究组 & 干预措施

High plant protein meal with additional leucine

Experimental

干预措施: High plant protein meal with additional leucine (Other)

Standard meal

Active Comparator

干预措施: Standard meal (Other)

High animal protein meal

Experimental

干预措施: High animal protein meal (Other)

High plant protein meal

Experimental

干预措施: High plant protein meal (Other)

结局指标

主要结局

Monocyte p-S6 content

时间窗: change from at 1 hour before meal intake and 3 hours after the meal

phospho-S6 content in monocytes

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Bettina Mittendorfer

Senior Associate Dean for Research

University of Missouri-Columbia

研究点 (2)

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