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临床试验/NCT03796455
NCT03796455已完成不适用

Effects of Low Dose of Fish Oil (EPA+DHA) vs. Combined EPA+DHA and HMB Supplementation on Protein Metabolism, Muscle Mass and Functional Capacity in Moderate to Severe COPD

Texas A&M University1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2018年4月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
54
试验地点
1
主要终点
Changes to net whole body protein metabolism

研究概览

简要总结

In the present study, the role of chronic (10 weeks) intake of low dose (2g/day) of EPA+DHA in whole body protein metabolism, and functional performance and systemic inflammation will be examined, and whether adding either HMB at 3.0 g/d to the low dose of EPA+DHA (2.0 g/d) will enhance these effects even more.

详细描述

Weight loss commonly occurs in patients with Chronic Obstructive Pulmonary Disease (COPD), negatively influencing their quality of life, treatment response and survival. Furthermore, limb muscle dysfunction (weakness and/or enhanced fatigue) is a major systemic comorbidity in patients with Chronic Obstructive Pulmonary Disease (COPD), negatively affecting their exercise performance, physical activity, quality of life, and mortality. As nutritional abnormalities are main contributors to muscle loss and dysfunction in COPD, nutritional support is viewed as an essential component of integrated care in these patients.

Although nutritional support is effective in the treatment of weight loss in COPD, attempts to increase muscle mass and function in COPD by supplying large amounts of protein or calories to these patients have been small. This suggests that gains in muscle mass and function are difficult to achieve in COPD unless specific metabolic abnormalities are targeted. The investigators and other researchers found that low muscle mass in COPD was strongly associated with elevated whole body protein turnover and increased myofibrillar protein breakdown rates indicative of muscle contractile protein loss. The investigators have extended this finding recently to normal weight COPD patients characterized by muscle weakness using a more precise and accurate pulse method of tau-methylhistidine tracer.

A substantial number of COPD patients, underweight as well as normal weight to obese, are characterized by an increased inflammatory response as evidenced by elevated levels of the pro-inflammatory cytokines (Tumor Necrosis Factor (TNF)-α, Interleukin (IL) 6 and 8, and the soluble TNF-α receptors (55 and 75). Furthermore, CRP levels are elevated in COPD and associated with reduced quadriceps strength, lower maximal and submaximal exercise capacity and increased morbidity.

One of the few agents capable to suppress the generation of pro-inflammatory cytokines are eicosapentanoic acid (EPA) and docosahexanoic acid (DHA), primary ω-3 fatty acids found in fish oils.

Previous experimental research and clinical studies in cachectic conditions (mostly malignancy) indicate that polyunsaturated fatty acids (PUFA) are able to attenuate protein degradation by improving the anabolic response to feeding and by decreasing the acute phase response. Eicosapentaenoic acid (EPA), in combination with docosahexaenoic acid (DHA), has been shown to effectively inhibit weight loss in several disease states, however weight weight and muscle mass and function increase was not present or minimal. Also in healthy older adults, fish oil can slow the decline in muscle mass and function. A randomized clinical trial in COPD patients showed that extra nutritional supplementation with PUFAs daily of 1000 mg EPA+DHA as adjunct to exercise training during 8 weeks enhanced exercise capacity but did not lead to muscle mass gain. The patients who did not respond adequately (< 2% gain in weight), had a higher TNF-α level than those who did gain sufficient weight, which is in line with previous data in COPD showing an association between an increased systemic inflammation with non-response to nutritional therapy.

研究设计

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

入排标准

年龄范围
45 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Ability to walk, sit down and stand up independently
  • •Ability to lie in supine or slightly elevated position for 8.5 hours
  • •Age 45 - 100
  • •Clinical diagnosis of COPD, including moderate to very severe chronic airflow limitation, and an FEV1 < 70% of reference FEV1 (GOLD II-III). If subjects are on β2 agonists, only those subjects with <10% improvement in FEV1 will be included.
  • •Clinically stable condition and not suffering from a respiratory tract infection or exacerbation of their disease (defined as a combination of increased cough, sputum purulence, shortness of breath, systemic symptoms such as fever, and a decrease in FEV1 > 10% compared with values when clinically stable in the preceding year) at least 4 weeks prior to the first test day
  • •Shortness of breath on exertion
  • •Willingness and ability to comply with the protocol, including:
  • •Refraining from intense physical activities (72h) prior to each study visit
  • •Adhering to fasting state and no smoking from 10 pm ± 2h onwards the day prior to each study visit

排除标准

  • •Participants 86 and older that fail to get physician approval
  • •Established diagnosis of malignancy
  • •Established diagnosis of Insulin Dependent Diabetes Mellitus
  • •History of untreated metabolic diseases including hepatic or renal disorder
  • •Presence of acute illness or metabolically unstable chronic illness
  • •Recent myocardial infarction (less than 1 year)
  • •Any other condition according to the PI or nurse that was found during the screening visit, that would interfere with the study or safety of the patient
  • •BMI ≥ 45 kg/m2
  • •Dietary or lifestyle characteristics:
  • •Daily use of supplements containing EPA+DHA or HMB prior to the first test day
  • •Use of protein or amino acid containing nutritional supplements within 5 days of first test day
  • •Indications related to interaction with study products. Known hypersensitivity to fish and/or shellfish and/or soy
  • •Use of long-term oral corticosteroids or short course of oral corticosteroids 4 weeks preceding first test day
  • •Failure to give informed consent or Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements

研究组 & 干预措施

Fish Oil

Experimental

2.0 g EPA + DHA / day + placebo powder

干预措施: Capsule + Powder supplementation (Dietary Supplement)

Fish Oil

Experimental

2.0 g EPA + DHA / day + placebo powder

干预措施: stable tracer infusion (Other)

Fish Oil and HMB

Experimental

2.0 g EPA + DHA + 3.0 g HMB / day

干预措施: Capsule + Powder supplementation (Dietary Supplement)

Fish Oil and HMB

Experimental

2.0 g EPA + DHA + 3.0 g HMB / day

干预措施: stable tracer infusion (Other)

Placebo

Placebo Comparator

3 g/d soy oil: corn oil (50:50 ratio) + placebo powder

干预措施: Capsule + Powder supplementation (Dietary Supplement)

Placebo

Placebo Comparator

3 g/d soy oil: corn oil (50:50 ratio) + placebo powder

干预措施: stable tracer infusion (Other)

结局指标

主要结局

Changes to net whole body protein metabolism

时间窗: baseline and after 10-week supplementation

whole body protein synthesis and myofibrillar protein breakdown measured by labeled amino acids on each study day via blood drawn at time 4, 10, 15, 20, 30, 40, 60, 120, 180, 240 minutes of infusion

次要结局

  • respiratory muscle strength(15 minutes on baseline visit, visit at week 5 of supplement intake, and after 10-week supplementation)
  • muscle mass(15 minutes on baseline visit, visit at week 5 of supplement intake, and after 10-week supplementation)
  • limb muscle strength(15 minutes on baseline visit, visit at week 5 of supplement intake, and after 10-week supplementation)
  • functional performance via six minute walk test(baseline visit, visit at week 5 of supplement intake, and after 10-week supplementation)
  • resting energy expenditure(baseline visit and after 10-week supplementation)
  • systemic inflammatory markers(baseline visit and after 10-week supplementation)

研究者

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

Marielle PKJ Engelen, PhD

Associate Professor

Texas A&M University

研究点 (1)

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