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Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity

BACKGROUND: Statins are commonly prescribed for primary and secondary prevention of atherosclerotic disease. They reduce cholesterol biosynthesis by inhibiting hydroxymethylglutaryl-coenzyme A-reductase (HMG-CoA-reductase) and therefore mevalonate synthesis. Several studies reported a small, but sig...

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Autores principales: Felder, Martina, Maushart, Claudia Irene, Gashi, Gani, Senn, Jaël Rut, Becker, Anton S., Müller, Julian, Balaz, Miroslav, Wolfrum, Christian, Burger, Irene A., Betz, Matthias Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631514/
https://www.ncbi.nlm.nih.gov/pubmed/34858338
http://dx.doi.org/10.3389/fendo.2021.765807
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author Felder, Martina
Maushart, Claudia Irene
Gashi, Gani
Senn, Jaël Rut
Becker, Anton S.
Müller, Julian
Balaz, Miroslav
Wolfrum, Christian
Burger, Irene A.
Betz, Matthias Johannes
author_facet Felder, Martina
Maushart, Claudia Irene
Gashi, Gani
Senn, Jaël Rut
Becker, Anton S.
Müller, Julian
Balaz, Miroslav
Wolfrum, Christian
Burger, Irene A.
Betz, Matthias Johannes
author_sort Felder, Martina
collection PubMed
description BACKGROUND: Statins are commonly prescribed for primary and secondary prevention of atherosclerotic disease. They reduce cholesterol biosynthesis by inhibiting hydroxymethylglutaryl-coenzyme A-reductase (HMG-CoA-reductase) and therefore mevalonate synthesis. Several studies reported a small, but significant increase in the diagnosis of diabetes mellitus with statin treatment. The molecular mechanisms behind this adverse effect are not yet fully understood. Brown adipose tissue (BAT), which plays a role in thermogenesis, has been associated with a reduced risk of insulin resistance. Statins inhibit adipose tissue browning and have been negatively linked to the presence of BAT in humans. We therefore speculated that inhibition of BAT by statins contributes to increased insulin resistance in humans. METHODS: A prospective study was conducted in 17 young, healthy men. After screening whether significant cold-induced thermogenesis (CIT) was present, participants underwent glucose tolerance testing (oGTT) and assessment of BAT activity by FDG-PET/MRI after cold-exposure and treatment with a β3-agonist. Fluvastatin 2x40mg per day was then administered for two weeks and oGTT and FDG-PET/MRI were repeated. RESULTS: Two weeks of fluvastatin treatment led to a significant increase in glucose area under the curve (AUC) during oGTT (p=0.02), reduction in total cholesterol and LDL cholesterol (both p<0.0001). Insulin AUC (p=0.26), resting energy expenditure (REE) (p=0.44) and diet induced thermogenesis (DIT) (p=0.27) did not change significantly. The Matsuda index, as an indicator of insulin sensitivity, was lower after fluvastatin intake, but the difference was not statistically significant (p=0.09). As parameters of BAT activity, mean standard uptake value (SUV(mean)) (p=0.12), volume (p=0.49) and total glycolysis (p=0.74) did not change significantly during the intervention. Matsuda index, was inversely related to SUV(mean) and the respiratory exchange ratio (RER) (both R(2 =) 0.44, p=0.005) at baseline, but not after administration of fluvastatin (R(2 =) 0.08, p=0.29, and R(2 =) 0.14, p=0.16, respectively). CONCLUSIONS: Treatment with fluvastatin for two weeks reduced serum lipid levels but increased glucose AUC in young, healthy men, indicating reduced glucose tolerance. This was not associated with changes in cold-induced BAT activity.
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spelling pubmed-86315142021-12-01 Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity Felder, Martina Maushart, Claudia Irene Gashi, Gani Senn, Jaël Rut Becker, Anton S. Müller, Julian Balaz, Miroslav Wolfrum, Christian Burger, Irene A. Betz, Matthias Johannes Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Statins are commonly prescribed for primary and secondary prevention of atherosclerotic disease. They reduce cholesterol biosynthesis by inhibiting hydroxymethylglutaryl-coenzyme A-reductase (HMG-CoA-reductase) and therefore mevalonate synthesis. Several studies reported a small, but significant increase in the diagnosis of diabetes mellitus with statin treatment. The molecular mechanisms behind this adverse effect are not yet fully understood. Brown adipose tissue (BAT), which plays a role in thermogenesis, has been associated with a reduced risk of insulin resistance. Statins inhibit adipose tissue browning and have been negatively linked to the presence of BAT in humans. We therefore speculated that inhibition of BAT by statins contributes to increased insulin resistance in humans. METHODS: A prospective study was conducted in 17 young, healthy men. After screening whether significant cold-induced thermogenesis (CIT) was present, participants underwent glucose tolerance testing (oGTT) and assessment of BAT activity by FDG-PET/MRI after cold-exposure and treatment with a β3-agonist. Fluvastatin 2x40mg per day was then administered for two weeks and oGTT and FDG-PET/MRI were repeated. RESULTS: Two weeks of fluvastatin treatment led to a significant increase in glucose area under the curve (AUC) during oGTT (p=0.02), reduction in total cholesterol and LDL cholesterol (both p<0.0001). Insulin AUC (p=0.26), resting energy expenditure (REE) (p=0.44) and diet induced thermogenesis (DIT) (p=0.27) did not change significantly. The Matsuda index, as an indicator of insulin sensitivity, was lower after fluvastatin intake, but the difference was not statistically significant (p=0.09). As parameters of BAT activity, mean standard uptake value (SUV(mean)) (p=0.12), volume (p=0.49) and total glycolysis (p=0.74) did not change significantly during the intervention. Matsuda index, was inversely related to SUV(mean) and the respiratory exchange ratio (RER) (both R(2 =) 0.44, p=0.005) at baseline, but not after administration of fluvastatin (R(2 =) 0.08, p=0.29, and R(2 =) 0.14, p=0.16, respectively). CONCLUSIONS: Treatment with fluvastatin for two weeks reduced serum lipid levels but increased glucose AUC in young, healthy men, indicating reduced glucose tolerance. This was not associated with changes in cold-induced BAT activity. Frontiers Media S.A. 2021-11-10 /pmc/articles/PMC8631514/ /pubmed/34858338 http://dx.doi.org/10.3389/fendo.2021.765807 Text en Copyright © 2021 Felder, Maushart, Gashi, Senn, Becker, Müller, Balaz, Wolfrum, Burger and Betz https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Felder, Martina
Maushart, Claudia Irene
Gashi, Gani
Senn, Jaël Rut
Becker, Anton S.
Müller, Julian
Balaz, Miroslav
Wolfrum, Christian
Burger, Irene A.
Betz, Matthias Johannes
Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity
title Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity
title_full Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity
title_fullStr Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity
title_full_unstemmed Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity
title_short Fluvastatin Reduces Glucose Tolerance in Healthy Young Individuals Independently of Cold Induced BAT Activity
title_sort fluvastatin reduces glucose tolerance in healthy young individuals independently of cold induced bat activity
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631514/
https://www.ncbi.nlm.nih.gov/pubmed/34858338
http://dx.doi.org/10.3389/fendo.2021.765807
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