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Selenium Supplementation in Chronic Obstructive Pulmonary Disease (COPD) Patients

Primary Purpose

Chronic Obstructive Pulmonary Disease, Cardiovascular Disease

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Selenium
Sponsored by
St. Joseph's Health Care London
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chronic Obstructive Pulmonary Disease focused on measuring Selenium, Chronic Obstructive Pulmonaary Disease, Cardiovascular Disease, Anti-oxidant, Pulmonary

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged 40 years or older (no upper limit). Established Respirologist-diagnosed mild or moderate COPD, according to the Canadian Thoracic Society (CTS) Lung Function Guidelines.(33) For a diagnosis of mild COPD, patients must have FEV1 60% to 79% predicted and FEV1 / FVC < 0.7. For a diagnosis of moderate COPD, patients must have FEV1 40% to 59% predicted and FEV1 / FVC < 0.7. Current or former smokers with > 20 pack-year smoking history. Ability to provide informed consent. Women subjects must be post-menopausal. Exclusion Criteria: Current or recent (within 4 weeks) acute exacerbation of chronic bronchitis Current daily use of mineral or vitamin + mineral supplements or other natural health products that provide a daily dose of selenium that is greater than 100 µg Current daily use of >5000 U of vitamin A, >1000 mg of vitamin C, or >800 U vitamin E Known significant co-morbidity such as renal (creatinine > 150 mol/L) or hepatic disease (AST or ALT >3 times normal). Measurement of these will be a requirement of the study. Creatinine and Alanine aminotransferase (ALT) will be measured at the beginning and at the end of the study. Known or suspected active cancer other than non-melanoma skin cancer. Other concurrent major respiratory diagnosis other than COPD/asthma. Plan to start statin drugs during the 12 weeks of study drug (may enroll if statins started >1 month before current study enrollment or deferred until study completion). Consumption of brazil nuts. Individuals who have homocystinuria On niacin at a daily dose of 500 mg or higher for hyperlipidemia. If you have allergies to products that contain dicalcium phosphate, talc sugarloaf, steric acid, or silica.

Sites / Locations

  • St. Joseph's Healthcare

Outcomes

Primary Outcome Measures

To determine whether 12 weeks of selenium supplementation increases GPx-1 levels compared with placebo

Secondary Outcome Measures

To determine whether selenium affects respiratory symptoms and function, and measures of inflammatory and infections markers.

Full Information

First Posted
September 10, 2005
Last Updated
May 21, 2008
Sponsor
St. Joseph's Health Care London
Collaborators
Father Sean O'Sullivan Research Centre
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1. Study Identification

Unique Protocol Identification Number
NCT00186706
Brief Title
Selenium Supplementation in Chronic Obstructive Pulmonary Disease (COPD) Patients
Official Title
The Effect of Selenium Supplementation on Anti-Oxidant Levels in COPD Patients: A 12-Week, Randomized, Placebo-Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2008
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
November 2007 (Actual)
Study Completion Date
November 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
St. Joseph's Health Care London
Collaborators
Father Sean O'Sullivan Research Centre

4. Oversight

5. Study Description

Brief Summary
Does an oral selenium supplement increase blood levels of antioxidants in patients with established, smoking-related lung disease? Members of our study group recently discovered that elevated levels of the anti-oxidant GPx-1 may be protective against heart disease. We are studying whether selenium supplementation will improve GPx-1 levels.
Detailed Description
Patients with chronic obstructive pulmonary disease (COPD) are at high risk for atherosclerotic heart disease, in part because of their nearly universal exposure to heavy smoking, and in part to other incompletely understood mechanisms which may include inflammation and anti-oxidant status. Smoking markedly affects both circulating inflammatory markers concentrations, and the anti-oxidant glutathione peroxidase-1 (GPx-1). We hypothesize that smoking-related inflammation and anti-oxidant consumption lead to both cardiovascular (CV) and respiratory disease. In a recent study, we (Blankenberg et al) found that higher levels of GPx-1 were associated with lower rates af future CV events and death. GPx-1 levels were lower among smokers, and the combination of current smoking and GPx-1 levels below the median was strongly (HR=5.6) and significantly associated with future CV events and death. There is a biological and epidemiological rationale to study selenium supplementation for CV protection. GPx-1 is a selenium-dependent enzyme, and data support the hypothesis that selenium supplementation increases GPx activity in various diseases. Furthermore, epidemiologic studies have discovered an inverse association between selenium content in soil and CV incidence and mortality. We hypothesize that selenium supplementation will elevate intra-erythrocytic GPx-1 levels in COPD patients and, ultimately, retard CV progression. In this study, we will test the first component of this assertion. In a randomized, placebo-controlled trial, we will determine whether 12 weeks of selenium supplementation increases GPx-1 levels among 120 COPD patients. If successful, this study may lead to future large clinical trials to assess whether selenium, an inexpensive and safe mineral, improves clinical outcomes in cardiovascular and respiratory disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease, Cardiovascular Disease
Keywords
Selenium, Chronic Obstructive Pulmonaary Disease, Cardiovascular Disease, Anti-oxidant, Pulmonary

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Selenium
Primary Outcome Measure Information:
Title
To determine whether 12 weeks of selenium supplementation increases GPx-1 levels compared with placebo
Secondary Outcome Measure Information:
Title
To determine whether selenium affects respiratory symptoms and function, and measures of inflammatory and infections markers.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged 40 years or older (no upper limit). Established Respirologist-diagnosed mild or moderate COPD, according to the Canadian Thoracic Society (CTS) Lung Function Guidelines.(33) For a diagnosis of mild COPD, patients must have FEV1 60% to 79% predicted and FEV1 / FVC < 0.7. For a diagnosis of moderate COPD, patients must have FEV1 40% to 59% predicted and FEV1 / FVC < 0.7. Current or former smokers with > 20 pack-year smoking history. Ability to provide informed consent. Women subjects must be post-menopausal. Exclusion Criteria: Current or recent (within 4 weeks) acute exacerbation of chronic bronchitis Current daily use of mineral or vitamin + mineral supplements or other natural health products that provide a daily dose of selenium that is greater than 100 µg Current daily use of >5000 U of vitamin A, >1000 mg of vitamin C, or >800 U vitamin E Known significant co-morbidity such as renal (creatinine > 150 mol/L) or hepatic disease (AST or ALT >3 times normal). Measurement of these will be a requirement of the study. Creatinine and Alanine aminotransferase (ALT) will be measured at the beginning and at the end of the study. Known or suspected active cancer other than non-melanoma skin cancer. Other concurrent major respiratory diagnosis other than COPD/asthma. Plan to start statin drugs during the 12 weeks of study drug (may enroll if statins started >1 month before current study enrollment or deferred until study completion). Consumption of brazil nuts. Individuals who have homocystinuria On niacin at a daily dose of 500 mg or higher for hyperlipidemia. If you have allergies to products that contain dicalcium phosphate, talc sugarloaf, steric acid, or silica.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marek J Smieja, MD PhD FRCPC
Organizational Affiliation
Associate Professor, Dept. of Pathology & Molecular Medicine, McMaster University; Microbiologist & Infectious Disease Physician, Dept. of Laboratory Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Joseph's Healthcare
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada

12. IPD Sharing Statement

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Selenium Supplementation in Chronic Obstructive Pulmonary Disease (COPD) Patients

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