Effect of SGLT2-Inhibitors on Epicardial Adipose Tissue: A Meta-Analysis

(1) Sodium–glucose cotransporter-2 inhibitors (SGLT2-i) reduce adipose tissue and cardiovascular events in patients with type 2 diabetes (T2D). Accumulation of epicardial adipose tissue (EAT) is associated with increased cardio-metabolic risks and obstructive coronary disease events in patients with...

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Published inCells (Basel, Switzerland) Vol. 10; no. 8; p. 2150
Main Authors Masson, Walter, Lavalle-Cobo, Augusto, Nogueira, Juan Patricio
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 20.08.2021
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Abstract (1) Sodium–glucose cotransporter-2 inhibitors (SGLT2-i) reduce adipose tissue and cardiovascular events in patients with type 2 diabetes (T2D). Accumulation of epicardial adipose tissue (EAT) is associated with increased cardio-metabolic risks and obstructive coronary disease events in patients with T2D. (2) We performed a systematic review and meta-analysis of SGLT2-i therapy on T2D patients, reporting data on changes in EAT after searching the PubMed/MEDLINE, Embase, Science Direct, Scopus, Google Scholar, and Cochrane databases. A random effects or fixed effects model meta-analysis was then applied. (3) Results: A total of three studies (n = 64 patients with SGLT2-i, n = 62 with standard therapy) were included in the final analysis. SGLT2 inhibitors reduced EAT (SMD: −0.82 (−1.49; −0.15); p < 0.0001). An exploratory analysis showed that HbA1c was significantly reduced with SGLT2-i use, while body mass index was not significantly reduced with this drug. (4) Conclusions: This meta-analysis suggests that the amount of EAT is significantly reduced in T2D patients with SGLT2-i treatment.
AbstractList (1) Sodium–glucose cotransporter-2 inhibitors (SGLT2-i) reduce adipose tissue and cardiovascular events in patients with type 2 diabetes (T2D). Accumulation of epicardial adipose tissue (EAT) is associated with increased cardio-metabolic risks and obstructive coronary disease events in patients with T2D. (2) We performed a systematic review and meta-analysis of SGLT2-i therapy on T2D patients, reporting data on changes in EAT after searching the PubMed/MEDLINE, Embase, Science Direct, Scopus, Google Scholar, and Cochrane databases. A random effects or fixed effects model meta-analysis was then applied. (3) Results: A total of three studies ( n = 64 patients with SGLT2-i, n = 62 with standard therapy) were included in the final analysis. SGLT2 inhibitors reduced EAT (SMD: −0.82 (−1.49; −0.15); p < 0.0001). An exploratory analysis showed that HbA1c was significantly reduced with SGLT2-i use, while body mass index was not significantly reduced with this drug. (4) Conclusions: This meta-analysis suggests that the amount of EAT is significantly reduced in T2D patients with SGLT2-i treatment.
(1) Sodium–glucose cotransporter-2 inhibitors (SGLT2-i) reduce adipose tissue and cardiovascular events in patients with type 2 diabetes (T2D). Accumulation of epicardial adipose tissue (EAT) is associated with increased cardio-metabolic risks and obstructive coronary disease events in patients with T2D. (2) We performed a systematic review and meta-analysis of SGLT2-i therapy on T2D patients, reporting data on changes in EAT after searching the PubMed/MEDLINE, Embase, Science Direct, Scopus, Google Scholar, and Cochrane databases. A random effects or fixed effects model meta-analysis was then applied. (3) Results: A total of three studies (n = 64 patients with SGLT2-i, n = 62 with standard therapy) were included in the final analysis. SGLT2 inhibitors reduced EAT (SMD: −0.82 (−1.49; −0.15); p < 0.0001). An exploratory analysis showed that HbA1c was significantly reduced with SGLT2-i use, while body mass index was not significantly reduced with this drug. (4) Conclusions: This meta-analysis suggests that the amount of EAT is significantly reduced in T2D patients with SGLT2-i treatment.
Author Masson, Walter
Nogueira, Juan Patricio
Lavalle-Cobo, Augusto
AuthorAffiliation 2 Endocrinology, Nutrition and Metabolism Investigation Center, Faculty of Health Science, National University of Formosa, Formosa 3600, Argentina
1 Council of Epidemiology and Cardiovascular Prevention, Argentine Society of Cardiology, Buenos Aires 1115, Argentina; walter.masson@hospitalitaliano.org.ar (W.M.); augustolavalle@gmail.com (A.L.-C.)
AuthorAffiliation_xml – name: 1 Council of Epidemiology and Cardiovascular Prevention, Argentine Society of Cardiology, Buenos Aires 1115, Argentina; walter.masson@hospitalitaliano.org.ar (W.M.); augustolavalle@gmail.com (A.L.-C.)
– name: 2 Endocrinology, Nutrition and Metabolism Investigation Center, Faculty of Health Science, National University of Formosa, Formosa 3600, Argentina
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Snippet (1) Sodium–glucose cotransporter-2 inhibitors (SGLT2-i) reduce adipose tissue and cardiovascular events in patients with type 2 diabetes (T2D). Accumulation of...
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SubjectTerms Adipose tissue
Bias
Body fat
Body mass index
Cardiovascular disease
Clinical trials
Diabetes
Diabetes mellitus (non-insulin dependent)
epicardial adipose tissue
Heart diseases
Heart failure
Kidney diseases
Meta-analysis
Mortality
Patients
Quantitative analysis
Reproducibility
sodium–glucose co-transporter-2 inhibitors
Systematic Review
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Title Effect of SGLT2-Inhibitors on Epicardial Adipose Tissue: A Meta-Analysis
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