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临床试验/NCT04364074
NCT04364074已完成不适用

Acute Impact of Probiotic Supplementation on Endothelial Function in Adults

Medical College of Wisconsin2 个研究点 分布在 1 个国家目标入组 26 人开始时间: 2020年8月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
26
试验地点
2
主要终点
change in baseline flow mediated dilation (FMD) after probiotic consumption

研究概览

简要总结

One in every two deaths in the United States is caused by cardiovascular disease. Despite strong mechanistic links established between a diet rich in lipids and the pathogenesis of cardiovascular disease, therapeutic advances have focused on reduction in either ingestion or synthesis of cholesterol, and reduction in dietary trans and saturated fatty acids and triglycerides. Even in the setting of aggressive high potency statin therapy and global cardiovascular risk reduction efforts, most clinical trials reveal a significant residual cardiovascular risk with, at best, only 30% reduction in major adverse cardiovascular events. There exists a significant unmet clinical need for identifying novel therapies for the prevention and treatment of cardiovascular disease. This requires identification of additional contributory processes to cardiovascular disease pathogenesis, so that mechanism-based interventions may be developed. Endothelial dysfunction is a pathological state in which there is systemic inflammation of vascular endothelium with consequent expression of pro-vasoconstrictive mediators, thrombotic and atherogenic tendencies. Endothelial dysfunction precedes the development of atherosclerosis and portends an increased risk of future adverse cardiovascular events. Endothelial dysfunction, therefore, can serve as a "barometer" of future cardiovascular risk. Measurement of Flow-mediated dilation ( FMD) is widely accepted as a method to assess vascular endothelial function.

详细描述

Researchers at MCW have discovered a new pathway that links the type of bacteria present in the intestines to the severity of heart attacks. This discovery of a relationship between intestinal bacteria, bacterial metabolites, and severity of heart attacks means that for the first time, we may be able to determine a person's probability of having a heart attack via non-conventional risk factors. This may provide opportunities for novel diagnostic tests as well as a potential for therapeutic intervention. The link between gut microbiota and the severity of heart attacks may also lead to novel therapeutic approaches (probiotics, non-absorbable antibiotics) to prevent heart attacks from happening. Our pilot study has demonstrated that supplementation of Lactobacillus plantarum 299v (Lp299v) for 6 weeks to adults with a history of coronary artery disease showed improvement in endothelial function. Whether acute ingestion of a single drink containing Lp299v supplementation favorably impacts vascular endothelial function is not known. The study proposed will test the hypothesis that supplementation of Lp299v favorably impacts vascular endothelial function after ingestion of a single supplement containing Lp299v.

Specific Aim 1 will determine the acute impact of probiotic supplementation on endothelial cell function as measured by brachial artery flow mediated dilation (FMD)

Specific Aim 2 will determine the impact of acute probiotic supplementation on blood biomarkers for inflammation.

Specific Aim 3 will be to determine the impact of baseline constitution of intestinal microbiota (assessed by stool microbiome) on change in FMD as a result of acute response to probiotic supplementation.

Specific Aim 4 will be to determine the impact of baseline constitution of intestinal microbiota (assessed by stool microbiome) on change in levels of blood markers for inflammation as a result of acute response probiotic supplementation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
21 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Have at least one of the following conditions:
  • Hypertension
  • Hyperlipidemia
  • Diabetes mellitus (Type 1 or Type 2)
  • Peripheral vascular disease
  • Cerebrovascular disease
  • Cardiovascular disease.

排除标准

  • Unstable angina or myocardial infarction by history, ECG, and/or enzymatic criteria within 1 month of enrollment.
  • LV dysfunction as defined by an LV ejection fraction documented as < 45% within 1 year of enrollment by an echocardiogram, MRI, or nuclear imaging.
  • Uncontrolled hypertension with blood pressure greater than 170/100 mmHg at the screening visit.
  • Known history of chronic renal insufficiency, liver dysfunction, or cancer besides non-melanoma skin carcinomas or localized prostate cancer requiring systemic treatment within five years of enrollment.
  • Known history of cognitive impairment or inability to follow study procedures
  • Patient with an implanted defibrillator or permanent pacemaker on which the potential participant is known to rely upon for greater than 50% of ventricular depolarizations.
  • Patients who received probiotics, prebiotics, and antibiotics in the last 12 weeks.
  • Patients with dosing changes of vasoactive medications and HMG-CoA reductase inhibitors in the 6 weeks prior to enrollment.
  • Pregnancy
  • Patients who are currently taking Vitamin K antagonists such as coumadin, warfarin.
  • Those who are daily drinkers.
  • Patients with gastrointestinal diseases that might alter the impact of a probiotic (e.g. status post colectomy, short gut syndrome, or inflammatory bowel disease)

结局指标

主要结局

change in baseline flow mediated dilation (FMD) after probiotic consumption

时间窗: from baseline to 24 hours after consumption and approximately 7 days after consumption

This is a measurement of endothelial function in the brachial artery

次要结局

  • Interleukin-12(from baseline to 24 hours after consumption and approximately 7 days after consumption)
  • Interleukin-6(from baseline to 24 hours after consumption and approximately 7 days after consumption)
  • Interleukin-8(from baseline to 24 hours after consumption and approximately 7 days after consumption)

研究者

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

Michael E. Widlansky

Professor

Medical College of Wisconsin

研究点 (2)

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