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Metformin to Reduce Airway Glucose in COPD Patients

Metformin to Reduce Airway Glucose in COPD Patients

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03651895
Enrollment
14
Registered
2018-08-29
Start date
2022-05-17
Completion date
2023-06-01
Last updated
2025-02-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary Disease

Keywords

Chronic Obstructive Pulmonary Disease

Brief summary

Chronic obstructive pulmonary disease (COPD) is the 4th leading cause of death worldwide and affects 1.2 million people in the UK, costing the NHS \>£800 million annually. COPD patients are more susceptible to bacterial infections and both chronic and acute infections are common. COPD patients with chronic lung bacterial infection have worse quality of life, faster disease progression, more symptoms and frequent exacerbations. Acute infections are the main cause of COPD exacerbations which cause COPD patients to become acutely unwell and often result in hospitalisation especially in the winter. Antibiotics are frequently used to treat COPD exacerbations and this contributes to the development of antibiotic resistance. Therefore there is a need to develop antibiotic-independent approaches to reducing or preventing bacterial infection in COPD. The investigators have carried out work in in animal studies and in humans showing that there is a link between high levels of glucose in the lung and bacterial lung infection. Levels of glucose in the lung are higher in COPD patients compared with people without COPD. These higher glucose levels support greater bacterial growth probably because glucose is a nutrient for bacteria. Therefore reducing airway glucose has the potential to inhibit bacterial growth in COPD patients. In animal studies the investigators have demonstrated that the diabetic drug metformin decreases airway glucose and bacterial growth. The investigators wish to determine if metformin can achieve the same effects in COPD patients. Metformin is safe and cheap, and has been extensively used in COPD patients with diabetes with an excellent safety record. The primary aim of this study will be to determine whether metformin reduces lung glucose in a small group of non-diabetic COPD patients. If it demonstrates that metformin reduces lung glucose concentrations it will justify a larger clinical trial of metformin as a treatment for COPD.

Detailed description

Chronic obstructive pulmonary disease (COPD) is the 4th leading cause of death worldwide and affects 1.2 million people in the UK, costing the NHS \>£800 million annually. COPD patients are more susceptible to both chronic and acute bacterial infections. Patients with chronic lung bacterial infection have worse quality of life, faster disease progression, more symptoms and frequent exacerbations. Acute infections are the main cause of acute COPD exacerbations which cause COPD patients to become acutely unwell and often result in hospitalisation especially in the winter. Bacteria are detected in 50-60% of COPD exacerbations. Antibiotics are frequently used to treat COPD exacerbations and this contributes to the development of antibiotic resistance. Therefore any intervention that prevents or reduces bacterial infection in COPD, especially if it is not an antibiotic, will have major benefits for COPD patients, the NHS and for society as a whole. It is likely that there are many reasons why COPD patients are more susceptible to bacterial infections. From experimental work the investigators have carried out one of the reasons may be high glucose concentrations in the lung. In healthy lungs glucose levels are kept low and this may be a mechanism that inhibits bacterial growth by depriving them of an essential nutrient. In animal studies the investigators have demonstrated that when levels of glucose in the lung are high, bacterial lung infection is more common. The investigators measured lung glucose concentrations in COPD patients and found that they are higher compared with people without COPD. COPD patients with higher levels of glucose also had more bacteria in their lungs and sputum samples from COPD patients with higher glucose concentrations supported greater bacterial growth in the laboratory. Therefore this study was the first to link elevated glucose in the lung to bacterial infection in COPD. Therefore reducing airway glucose has the potential to inhibit bacterial growth in COPD patients. Study Design The proposed study will be a randomised, double-blinded, placebo-controlled, cross-over study of metformin in COPD patients. The primary outcome will be sputum glucose after 3 months' treatment with metformin compared with sputum glucose in those taking placebo. In order to account for potential withdrawals 40 subjects will be recruited. Study Procedures Potential participants will attend for a screening visit where they will have a full medical history, a physical examination and spirometry carried out to confirm the diagnosis of COPD. A blood test will also be done to measure kidney and liver function and blood glucose to exclude undiagnosed diabetes, kidney disease or liver disease. If they fulfil the entry criteria and consent to taking part in the study they will have a baseline visit prior to being randomised. The baseline visit will include: 1. Physical examination and measurement of vital signs 2. Completion of quality of life (St George's Respiratory Questionnaire (SGRQ)) and symptom questionnaires (COPD Assessment Test (CAT)) 3. Collection of samples. The samples collected will include blood samples, nose samples collected using nasal synthetic absorption matrix (SAM) strips and induced sputum. After baseline assessment, subjects will either be commenced on metformin (500mg twice a day after meals) or placebo for 3 months during which time the participants will have monthly visits. At these visits the same assessments and sampling as the baseline will be carried out, together with collection of data regarding exacerbations and adverse events. Following a 2 week washout period the subjects will crossover to the other study arm for another 3 months and follow the same study protocol.

Interventions

DRUGMetformin

The Drug was administered 500 mg twice daily for one week and increased to 1g twice daily for the reminder of the 3 months.

DRUGPlacebo

Placebo

Sponsors

Imperial College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Age between 40 and 75 years * Clinical diagnosis of COPD confirmed with spirometry (Post-bronchodilator FEV1/FVC \<70%). * Smoking history \>15 pack years * Absence of infection \>8 weeks prior to study entry * No use of antibiotics and/or oral corticosteroids \>8 weeks prior to study entry * Able to understand and consent to the study procedures

Exclusion criteria

* Diabetes including diabetes diagnosed at screening * History of hepatic or renal impairment or diagnosed on screening bloods * Patients already taking metformin irrespective of indication * Known allergy or hypersensitivity to metformin * Pregnancy or breastfeeding * Any other significant medical condition likely to interfere with the study * Unable to provide informed consent * Excessive alcohol intake (\>21 units/week) * BMI \< 18.5kg/m2

Design outcomes

Primary

MeasureTime frameDescription
Sputum Glucose Concentration3 monthsThe median concentration of glucose in sputum following 3 months treatment with metformin or placebo.

Secondary

MeasureTime frameDescription
Sputum Bacterial Load3 monthsThe bacterial load in sputum using qPCR was not measured. Therefore, data were not collected
Sputum Inflammatory Markers3 monthsThe median concentration of inflammatory cells and cytokines in sputum was not measured. Therefore, data were not collected.
Nasal Glucose Concentrations3 monthsThe median concentration of glucose in nasal samples following 3 months treatment with metformin or placebo.
Quality of Life Score (St George's Respiratory Questionnaire)1 monthSt George's Respiratory Questionnaire (SGRQ): the SGRQ contains 50 items with a minimum score of 0 and a maximum score of 100. Higher scores indicate a greater impact on quality of life due to COPD and a difference of ≥4 is meaningful The questionnaire's were completed by every participant at every visit up to 8 times: V1 is at the baseline, then V2-4 are at monthly intervals. V5 is at the baseline after crossing arms -1 month washout, V6-8 are monthly after that.
Lung Function1 monthFEV1(Forced Expiratory Volume Test) was performed up to 8 times: V1 is at the baseline, then V2-4 are at monthly intervals. V5 is at the baseline after crossing arms -1 month washout, V6-8 are monthly after that.
Quality of Life Score (COPD Assessment Test)1 monthThe COPD Assessment Test (CAT): the CAT features 8 questions ranked from 0-5 with a minimum score of 0 and maximum possible score of 40. Higher scores indicate a greater impact on patient health due to their COPD, a difference of ≥2 is considered meaningful. The questionnaire's were completed by every participant at every visit up to 8 times: V1 is at the baseline, then V2-4 are at monthly intervals. V5 is at the baseline after crossing arms -1 month washout, V6-8 are monthly after that.

Countries

United Kingdom

Participant flow

Recruitment details

Overall treatment time 6 months (2 milestones at 1 and 3 months)

Pre-assignment details

14 participants were enrolled but 11 withdrew for lower/upper respiratory tract infections (LRTI/URTI) Cough and Vomiting. At 3 months there was a washout and a crossover thereafter.

Participants by arm

ArmCount
Treatment Group & Placebo Group
Placebo Or Metformin 500mg/1g bd Metformin: The Drug was administered 500 mg twice daily for one week and increased to 1g twice daily for the reminder of the 3 months.
14
Total14

Withdrawals & dropouts

PeriodReasonFG000FG001
First Drug AssignmentAdverse Event45
Second Drug Assignment - CrossoverAdverse Event11

Baseline characteristics

CharacteristicTreatment Group & Placebo Group
Age, Customized
Age
67.9 years
COPD Assessment Test (CAT)15.4 Score on a scale
STANDARD_DEVIATION 9.3
Forced Expiratory Volume in One Second (FEV1) Percentage (%) Predicted68.2 Percentage(%) predicted
STANDARD_DEVIATION 17.8
Forced Vital Capacity (FVC) Percentage (%) Predicted100.3 Percentage (%) predicted
STANDARD_DEVIATION 15.1
Peak Expiratory Flow (PEF) Percentage (%) Predicted65.4 Percentage (%) predicted
STANDARD_DEVIATION 22.8
Race/Ethnicity, Customized
Others
2 Participants
Race/Ethnicity, Customized
White
12 Participants
Region of Enrollment
United Kingdom
14 participants
Sex: Female, Male
Female
10 Participants
Sex: Female, Male
Male
4 Participants
Sputum Glucose Concentration5.3 µmol
St George's Respiratory Questionnaire (SGRQ)41.8 Score on a scale
STANDARD_DEVIATION 16.2

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 140 / 14
other
Total, other adverse events
7 / 147 / 14
serious
Total, serious adverse events
0 / 141 / 14

Outcome results

Primary

Sputum Glucose Concentration

The median concentration of glucose in sputum following 3 months treatment with metformin or placebo.

Time frame: 3 months

ArmMeasureValue (MEDIAN)
Treatment GroupSputum Glucose Concentration68.92 µM
Placebo GroupSputum Glucose Concentration12.2 µM
Secondary

Lung Function

FEV1(Forced Expiratory Volume Test) was performed up to 8 times: V1 is at the baseline, then V2-4 are at monthly intervals. V5 is at the baseline after crossing arms -1 month washout, V6-8 are monthly after that.

Time frame: 1 month

ArmMeasureValue (MEDIAN)
Treatment GroupLung Function69.2 Litres (L)
Placebo GroupLung Function66.1 Litres (L)
Secondary

Nasal Glucose Concentrations

The median concentration of glucose in nasal samples following 3 months treatment with metformin or placebo.

Time frame: 3 months

ArmMeasureValue (MEDIAN)
Treatment GroupNasal Glucose Concentrations12.56 µM
Placebo GroupNasal Glucose Concentrations13.5 µM
Secondary

Quality of Life Score (COPD Assessment Test)

The COPD Assessment Test (CAT): the CAT features 8 questions ranked from 0-5 with a minimum score of 0 and maximum possible score of 40. Higher scores indicate a greater impact on patient health due to their COPD, a difference of ≥2 is considered meaningful. The questionnaire's were completed by every participant at every visit up to 8 times: V1 is at the baseline, then V2-4 are at monthly intervals. V5 is at the baseline after crossing arms -1 month washout, V6-8 are monthly after that.

Time frame: 1 month

ArmMeasureValue (MEDIAN)
Treatment GroupQuality of Life Score (COPD Assessment Test)16.6 Score on a scale
Placebo GroupQuality of Life Score (COPD Assessment Test)13.2 Score on a scale
Secondary

Quality of Life Score (St George's Respiratory Questionnaire)

St George's Respiratory Questionnaire (SGRQ): the SGRQ contains 50 items with a minimum score of 0 and a maximum score of 100. Higher scores indicate a greater impact on quality of life due to COPD and a difference of ≥4 is meaningful The questionnaire's were completed by every participant at every visit up to 8 times: V1 is at the baseline, then V2-4 are at monthly intervals. V5 is at the baseline after crossing arms -1 month washout, V6-8 are monthly after that.

Time frame: 1 month

ArmMeasureValue (MEDIAN)
Treatment GroupQuality of Life Score (St George's Respiratory Questionnaire)42.7 Score on a scale
Placebo GroupQuality of Life Score (St George's Respiratory Questionnaire)36.4 Score on a scale
Secondary

Sputum Bacterial Load

The bacterial load in sputum using qPCR was not measured. Therefore, data were not collected

Time frame: 3 months

Population: Data were not collected. Participants with infection were excluded from the study.

Secondary

Sputum Inflammatory Markers

The median concentration of inflammatory cells and cytokines in sputum was not measured. Therefore, data were not collected.

Time frame: 3 months

Population: Data were not collected. Participants with infection were excluded from the study.

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026