Dapagliflozin for Long COVID Syndrome
- Funded by Canadian Institutes of Health Research (CIHR)
- Total publications:0 publications
Grant number: 498296
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Key facts
Disease
COVID-19start year
2023Known Financial Commitments (USD)
$74,067.61Funder
Canadian Institutes of Health Research (CIHR)Principal Investigator
Paterson Ian, Thompson Richard BResearch Location
CanadaLead Research Institution
University of Ottawa Heart InstituteResearch Priority Alignment
N/A
Research Category
Clinical characterisation and management
Research Subcategory
Post acute and long term health consequences
Special Interest Tags
N/A
Study Type
Clinical
Clinical Trial Details
Randomized Controlled Trial
Broad Policy Alignment
Pending
Age Group
Unspecified
Vulnerable Population
Other
Occupations of Interest
Unspecified
Abstract
An estimated 30 million Canadians have been infected by the virus causing COVID-19 since the start of the pandemic. A recent Canadian survey found that 10-30% of COVID survivors describe long-term symptoms, with daily activities often limited by fatigue and shortness of breath. This condition is referred to as long COVID syndrome. Other studies have also shown that patients have a 50-70% higher risk for diabetes and heart disease in the first 12 months following COVID-19 infection. We recently evaluated 215 patients at 3-6 months post-COVID-19 infection and compared them to 133 patients without prior COVID-19. We performed whole body MRI and found significant abdominal fat accumulation in patients with prior COVID-19. Abdominal fat has been linked to a number of health issues including an increased risk for diabetes and heart disease. We also found that fat accumulation in the leg muscles was associated with long COVID symptom severity. We are the first group to identify these abnormalities in patients with prior COVID-19 infection. Dapagliflozin is a drug therapy that reduces the risk of heart disease in patients with diabetes and it has also been shown to reduce fat volumes in the abdomen. This medication has been studied in patients with acute COVID and was shown to be safe. However, dapagliflozin has not been evaluated in patients with long COVID syndrome. For this study, we will recruit 706 patients with long COVID syndrome and randomly assign them to 12 months of dapagliflozin or a placebo pill. All patients will undergo MRI to assess fat content in their abdomen and leg muscles. We expect to find that patients taking dapagliflozin will have lower abdominal fat and a lower risk for developing diabetes and heart disease. If dapagliflozin is found to be effective then it would be the first proven treatment of long COVID syndrome. It could immediately be used to help patients with this poorly understood condition.