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Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes

Bariatric surgery improves glycemic control better than medical therapy; however, the effect of bariatric surgery on HDL function is not well characterized. Serum samples were available at baseline, 1-, and 5-years post procedures, for 90 patients with obesity and type 2 diabetes who were randomized...

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Autores principales: Lorkowski, Shuhui Wang, Brubaker, Gregory, Rotroff, Daniel M., Kashyap, Sangeeta R., Bhatt, Deepak L., Nissen, Steven E., Schauer, Philip R., Aminian, Ali, Smith, Jonathan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226587/
https://www.ncbi.nlm.nih.gov/pubmed/32260470
http://dx.doi.org/10.3390/biom10040551
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author Lorkowski, Shuhui Wang
Brubaker, Gregory
Rotroff, Daniel M.
Kashyap, Sangeeta R.
Bhatt, Deepak L.
Nissen, Steven E.
Schauer, Philip R.
Aminian, Ali
Smith, Jonathan D.
author_facet Lorkowski, Shuhui Wang
Brubaker, Gregory
Rotroff, Daniel M.
Kashyap, Sangeeta R.
Bhatt, Deepak L.
Nissen, Steven E.
Schauer, Philip R.
Aminian, Ali
Smith, Jonathan D.
author_sort Lorkowski, Shuhui Wang
collection PubMed
description Bariatric surgery improves glycemic control better than medical therapy; however, the effect of bariatric surgery on HDL function is not well characterized. Serum samples were available at baseline, 1-, and 5-years post procedures, for 90 patients with obesity and type 2 diabetes who were randomized to intensive medical therapy (n = 20), Roux-en-Y gastric bypass (RYGB, n = 37), or sleeve gastrectomy (SG, n = 33) as part of the STAMPEDE clinical trial. We examined serum HDL function by two independent assays, apolipoprotein A-1 exchange rate (AER) and cholesterol efflux capacity (CEC). Compared with baseline, AER was significantly higher at 5 years for participants in all treatment groups, but only increased significantly at 1 year in the RYGB and SG groups. CEC was divided into ABCA1-dependent and independent fractions, and the later was correlated with AER. ABCA1-independent CEC increased significantly only at 5 years in both surgical groups, but did not significantly change in the medical therapy group. There was no significant change in ABCA1-dependent CEC in any group. The increase in AER, but not ABCA1-independent CEC, was correlated with the reduction in body mass index and glycated hemoglobin levels among all subjects at 5 years, indicating that AER as a measure of HDL function would be a better reflection of therapy versus CEC.
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spelling pubmed-72265872020-05-18 Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes Lorkowski, Shuhui Wang Brubaker, Gregory Rotroff, Daniel M. Kashyap, Sangeeta R. Bhatt, Deepak L. Nissen, Steven E. Schauer, Philip R. Aminian, Ali Smith, Jonathan D. Biomolecules Article Bariatric surgery improves glycemic control better than medical therapy; however, the effect of bariatric surgery on HDL function is not well characterized. Serum samples were available at baseline, 1-, and 5-years post procedures, for 90 patients with obesity and type 2 diabetes who were randomized to intensive medical therapy (n = 20), Roux-en-Y gastric bypass (RYGB, n = 37), or sleeve gastrectomy (SG, n = 33) as part of the STAMPEDE clinical trial. We examined serum HDL function by two independent assays, apolipoprotein A-1 exchange rate (AER) and cholesterol efflux capacity (CEC). Compared with baseline, AER was significantly higher at 5 years for participants in all treatment groups, but only increased significantly at 1 year in the RYGB and SG groups. CEC was divided into ABCA1-dependent and independent fractions, and the later was correlated with AER. ABCA1-independent CEC increased significantly only at 5 years in both surgical groups, but did not significantly change in the medical therapy group. There was no significant change in ABCA1-dependent CEC in any group. The increase in AER, but not ABCA1-independent CEC, was correlated with the reduction in body mass index and glycated hemoglobin levels among all subjects at 5 years, indicating that AER as a measure of HDL function would be a better reflection of therapy versus CEC. MDPI 2020-04-04 /pmc/articles/PMC7226587/ /pubmed/32260470 http://dx.doi.org/10.3390/biom10040551 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lorkowski, Shuhui Wang
Brubaker, Gregory
Rotroff, Daniel M.
Kashyap, Sangeeta R.
Bhatt, Deepak L.
Nissen, Steven E.
Schauer, Philip R.
Aminian, Ali
Smith, Jonathan D.
Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes
title Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes
title_full Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes
title_fullStr Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes
title_full_unstemmed Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes
title_short Bariatric Surgery Improves HDL Function Examined by ApoA1 Exchange Rate and Cholesterol Efflux Capacity in Patients with Obesity and Type 2 Diabetes
title_sort bariatric surgery improves hdl function examined by apoa1 exchange rate and cholesterol efflux capacity in patients with obesity and type 2 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226587/
https://www.ncbi.nlm.nih.gov/pubmed/32260470
http://dx.doi.org/10.3390/biom10040551
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