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Effect of 26 Weeks of Liraglutide Treatment on Coronary Artery Inflammation in Type 2 Diabetes Quantified by [ 64 Cu]Cu-DOTATATE PET/CT: Results from the LIRAFLAME Trial
Quantification of coronary artery inflammation and atherosclerosis remains a challenge in high-risk individuals. In this study we sought to investigate if the glucagon like peptide-1 receptor agonist liraglutide has a direct anti-inflammatory effect in the coronary arteries using positron emission t...
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Published in: | Frontiers in endocrinology (Lausanne) 2021-11, Vol.12, p.790405-790405 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Quantification of coronary artery inflammation and atherosclerosis remains a challenge in high-risk individuals. In this study we sought to investigate if the glucagon like peptide-1 receptor agonist liraglutide has a direct anti-inflammatory effect in the coronary arteries using positron emission tomography (PET) with a radioactive tracer targeting activated macrophages in the vessel-wall.
Thirty randomly selected participants with type 2 diabetes from the placebo-controlled trial LIRAFLAME were enrolled in this sub-study. Participants were, prior to enrollment in this sub-study, randomized to either treatment with daily liraglutide (n=15) or placebo (n=15). Both groups underwent a combined [
Cu]Cu-DOTATATE positron emission tomography and computed tomography scan of the heart at baseline and after 26 weeks of treatment. Coronary artery uptake of [
Cu]Cu-DOTATATE were measured as maximum standardized uptake values (SUV
); and means of the maximum values (mSUV
), both values were calculated at the level of each participant and each individual coronary-segment.
SUV
and mSUV
values decreased significantly in the liraglutide group both at the participant level (SUV
: p=0.013; mSUV
: p=0.004) and at the coronary-segment level (SUV
: p=0.001; mSUV
: p |
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ISSN: | 1664-2392 1664-2392 |
DOI: | 10.3389/fendo.2021.790405 |