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Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion

AIMS: Hyperproinsulinaemia is associated with obesity and is a risk factor for Type 2 diabetes. We explored the dynamics of proinsulin and insulin and postprandial effects on glucose and lipids in subjects who had undergone gastric bypass (GBP) surgery compared with morbidly obese (MO) subjects and...

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Autores principales: Johansson, H-E., Öhrvall, M., Haenni, A., Sundbom, M., Edén Engström, B., Karlsson, F. A., Zethelius, B.
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2121126/
https://www.ncbi.nlm.nih.gov/pubmed/17894830
http://dx.doi.org/10.1111/j.1464-5491.2007.02240.x
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author Johansson, H-E.
Öhrvall, M.
Haenni, A.
Sundbom, M.
Edén Engström, B.
Karlsson, F. A.
Zethelius, B.
author_facet Johansson, H-E.
Öhrvall, M.
Haenni, A.
Sundbom, M.
Edén Engström, B.
Karlsson, F. A.
Zethelius, B.
author_sort Johansson, H-E.
collection PubMed
description AIMS: Hyperproinsulinaemia is associated with obesity and is a risk factor for Type 2 diabetes. We explored the dynamics of proinsulin and insulin and postprandial effects on glucose and lipids in subjects who had undergone gastric bypass (GBP) surgery compared with morbidly obese (MO) subjects and normal weight control subjects (NW). METHODS: Subjects free from diabetes were recruited: 10 previously MO subjects [body mass index (BMI)±sd, 34.8±6.2kg/m(2)] who had undergone GBP surgery, 10 MO subjects (BMI 44±3.1kg/m(2)) and 12 NW control subjects (BMI 23.2±2.4kg/m(2)). After an overnight fast, a standard meal (2400 kJ) was ingested and glucose, proinsulin, insulin free fatty acids and triglycerides were determined up to 180 min. RESULTS: Fasting proinsulin was similar in the GBP group and NW control subjects, but threefold increased in MO subjects (P < 0.05). Postprandial AUC for glucose was similar in the three groups and AUC for proinsulin was high in MO, intermediate in the GBP group and lowest in NW control subjects (P for trend = 0.020). Postprandial proinsulin at 60 min was similar in the GBP group and MO subjects and twofold higher than in NW control subjects. Postprandial proinsulin at 180 min was normal in the GBP group, but fivefold increased in MO subjects (P = 0.008). Insulin increased rapidly at 30 min in the GBP group and was normal at 90 min, whereas insulin was still increased at 90–180 min in the MO subjects (P < 0.001). CONCLUSIONS: MO subjects, free from diabetes, have elevated proinsulin concentrations in the fasting as well as the postprandial phase. After GBP surgery markedly lower fasting and postprandial proinsulin concentrations were observed, although BMI was higher compared with NW control subjects.
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spelling pubmed-21211262007-12-11 Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion Johansson, H-E. Öhrvall, M. Haenni, A. Sundbom, M. Edén Engström, B. Karlsson, F. A. Zethelius, B. Diabet Med Original Articles AIMS: Hyperproinsulinaemia is associated with obesity and is a risk factor for Type 2 diabetes. We explored the dynamics of proinsulin and insulin and postprandial effects on glucose and lipids in subjects who had undergone gastric bypass (GBP) surgery compared with morbidly obese (MO) subjects and normal weight control subjects (NW). METHODS: Subjects free from diabetes were recruited: 10 previously MO subjects [body mass index (BMI)±sd, 34.8±6.2kg/m(2)] who had undergone GBP surgery, 10 MO subjects (BMI 44±3.1kg/m(2)) and 12 NW control subjects (BMI 23.2±2.4kg/m(2)). After an overnight fast, a standard meal (2400 kJ) was ingested and glucose, proinsulin, insulin free fatty acids and triglycerides were determined up to 180 min. RESULTS: Fasting proinsulin was similar in the GBP group and NW control subjects, but threefold increased in MO subjects (P < 0.05). Postprandial AUC for glucose was similar in the three groups and AUC for proinsulin was high in MO, intermediate in the GBP group and lowest in NW control subjects (P for trend = 0.020). Postprandial proinsulin at 60 min was similar in the GBP group and MO subjects and twofold higher than in NW control subjects. Postprandial proinsulin at 180 min was normal in the GBP group, but fivefold increased in MO subjects (P = 0.008). Insulin increased rapidly at 30 min in the GBP group and was normal at 90 min, whereas insulin was still increased at 90–180 min in the MO subjects (P < 0.001). CONCLUSIONS: MO subjects, free from diabetes, have elevated proinsulin concentrations in the fasting as well as the postprandial phase. After GBP surgery markedly lower fasting and postprandial proinsulin concentrations were observed, although BMI was higher compared with NW control subjects. Blackwell Publishing Ltd 2007-11 /pmc/articles/PMC2121126/ /pubmed/17894830 http://dx.doi.org/10.1111/j.1464-5491.2007.02240.x Text en © 2007 The Authors. Journal compilation © 2007 Diabetes UK https://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Articles
Johansson, H-E.
Öhrvall, M.
Haenni, A.
Sundbom, M.
Edén Engström, B.
Karlsson, F. A.
Zethelius, B.
Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
title Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
title_full Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
title_fullStr Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
title_full_unstemmed Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
title_short Gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
title_sort gastric bypass alters the dynamics and metabolic effects of insulin and proinsulin secretion
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2121126/
https://www.ncbi.nlm.nih.gov/pubmed/17894830
http://dx.doi.org/10.1111/j.1464-5491.2007.02240.x
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