AECOPD and Nutritional Supplementation in COPD

NCT ID: NCT06801964

Last Updated: 2025-01-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 5 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-10-20
• Study Completion Date: 2019-01-08

Brief Summary

Better understanding of the duration needed to overcome metabolic disturbances in patients experiencing exacerbation. Also, the explore role of nutritional intervention in the treatment program of stable COPD patients and in those recovering from an acute exacerbation (AECOPD) is important to restore loss of muscle mass and function and to reduce readmission and hospitalization rate of these patients, thereby leading to improved clinical and overall outcome as well as reduction of health care costs.

Detailed Description

Based on the literature, the Investigators hypothesize that an AECOPD is associated with an acute inflammatory response, accelerated muscle protein loss and compromised NO production and glutathione synthesis as compared to a stable COPD and healthy control group. Two weeks after AECOPD these disturbances are only partially restored and therefore nutritional intervention is required. Supplementation with milk proteins (containing essential amino acids) / carbohydrate (CHO) mixture in combination with fish oil supplementation will reduce the metabolic alterations in COPD patients recovering from an acute exacerbation but also in stable COPD as chronic systemic inflammation is also present in these patients. By simultaneously attenuating the catabolic effects of inflammation by fish oil and increasing the anabolic stimulus by high quality protein intake, muscle mass and function, will be restored, leading to better physical performance, condition and quality of life in COPD.

Specific aims:

• Specific aim 1: To test the hypothesis that AECOPD in outpatients results in severe net protein catabolism, impaired NO synthesis and GSH synthesis as compared to stable COPD. These disturbances are associated with impaired nutritional and functional status, and quality of life in COPD.
• Specific aim 2: To test the hypothesis that 14 days after AECOPD these disturbances are partially restored but still not comparable to that in stable chronic COPD patients and healthy control subjects. One group of participants with AECOPD will also be tested 10 weeks after exacerbation to see if metabolic disturbances have been restored.
• Specific aim 3: To test the effects of 8 weeks of nutritional supplementation with high-quality milk proteins (containing essential amino acids)/ carbohydrate (CHO) mixture with or without fish oil supplementation on protein and amino acid metabolism, muscle mass, muscle and cognitive function, physical performance, quality of life, and clinical and overall outcome in stable COPD patients and in those recovering from AECOPD.

Conditions

Obstructive Pulmonary Disease; Exacerbation Copd

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

AECOPD - No Nutrition

Group Type: EXPERIMENTAL

Stable isotope infusion

Intervention Type: OTHER

such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline

AECOPD - Nutrition

Group Type: EXPERIMENTAL

Stable isotope infusion

Intervention Type: OTHER

such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline

Protein and Fish Oil

Intervention Type: DIETARY_SUPPLEMENT

milk/carbohydrate mixture and supplementation of 3.5g of EPA+DHA (7g of fish oil)

Protein and Olive Oil

Intervention Type: DIETARY_SUPPLEMENT

milk/carbohydrate mixture with olive oil

Carbohydrate and Olive Oil

Intervention Type: DIETARY_SUPPLEMENT

carbohydrate mixture with olive oil

stable COPD

Group Type: EXPERIMENTAL

Stable isotope infusion

Intervention Type: OTHER

such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline

Protein and Fish Oil

Intervention Type: DIETARY_SUPPLEMENT

milk/carbohydrate mixture and supplementation of 3.5g of EPA+DHA (7g of fish oil)

Protein and Olive Oil

Intervention Type: DIETARY_SUPPLEMENT

milk/carbohydrate mixture with olive oil

Carbohydrate and Olive Oil

Intervention Type: DIETARY_SUPPLEMENT

carbohydrate mixture with olive oil

Healthy

Group Type: OTHER

Stable isotope infusion

Intervention Type: OTHER

such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline

Interventions

Stable isotope infusion

such as glycerol, D2O, tyrosine, phenylalanine, glucose, arginine, and citrulline

Intervention Type: OTHER

Protein and Fish Oil

milk/carbohydrate mixture and supplementation of 3.5g of EPA+DHA (7g of fish oil)

Intervention Type: DIETARY_SUPPLEMENT

Protein and Olive Oil

milk/carbohydrate mixture with olive oil

Intervention Type: DIETARY_SUPPLEMENT

Carbohydrate and Olive Oil

carbohydrate mixture with olive oil

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• Between age 45 and older
• Experiencing an acute exacerbation of COPD (defined as a combination of symptoms such as 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 years) and admitted at College Station Medical Center (with expected stay less than 10 days) or staying at home.
• Willingness and ability to comply with the protocol, including:
• Adhering to fasting state from 10 pm ± 2h onwards the day prior to each study visit
• Ability to lie in supine or elevated position for 4 hours

• Ability to walk, sit down and stand up independently
• Between age 45 and older
• Diagnosis of moderate to very severe chronic airflow limitation and compliant to the following criteria: FEV1 < 70% of reference FEV1
• Clinically stable condition and not suffering from a respiratory tract infection or exacerbation of their disease at least 4 weeks prior to the first test day
• Shortness of breath on exertion
• Willingness and ability to comply with the protocol, including:
• Adhering to fasting state from 10 pm ± 2h onwards the day prior to each study visit
• Ability to lie in supine or elevated position for 4 hours

• Healthy male or female according to the investigator's or appointed staff's judgment
• Ability to walk, sit down and stand up independently
• Between age 45 and older
• No diagnosis of chronic airflow limitation
• Willingness and ability to comply with the protocol, including:
• Adhering to fasting state from 10 pm ± 2h onwards the day prior to each study visit
• Ability to lie in supine or elevated position for 4 hours

Exclusion Criteria

• Any condition that may interfere with the definition 'healthy subject' according to the investigator's judgment (for healthy control group only)
• Established diagnosis of malignancy
• History of untreated metabolic diseases including hepatic or renal disorder
• Presence of other acute metabolic illnesses (ie renal, liver disease)
• 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
• Dietary or lifestyle characteristics:
• Current alcohol or drug abuse
• Known hypersensitivity to fish and/or shellfish, Swanson EFAs Super EPA Fish oil or any of its ingredients, Swanson EFAs Certified Organic Extra Virgin Olive oil or any of its ingredients or Smartfish Nutrifriend or any of its ingredients (AECOPD and stable COPD nutrition groups only)
• Use of supplements containing more than 1 g of EPA+DHA 3 months prior to the first test day (AECOPD and stable COPD nutrition groups only)
• Failure to give informed consent or Investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements
• (Possible) pregnancy
• Body mass index <18.5 or >45 kg/m2

• Minimum Eligible Age: 45 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Texas A&M University

OTHER

Sponsor Role: lead

Responsible Party

Marielle PKJ Engelen, PhD

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Marielle Engelen

Role: PRINCIPAL_INVESTIGATOR

Texas A&M University

Locations

Texas A&M University

College Station, Texas, United States

Countries

United States

Other Identifiers

2014-0139

Identifier Type: -

Identifier Source: org_study_id