Diabetes and dyslipidemia: characterizing lipoprotein metabolism

GH Tomkin,1,2 D Owens1,2 1Diabetes Institute of Ireland, Beacon Hospital, 2Trinity College, University of Dublin, Dublin, Ireland Abstract: Premature atherosclerosis in diabetes accounts for much of the decreased life span. New treatments have reduced this risk considerably. This review explores the...

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Autores principales: Tomkin GH, Owens D
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Lenguaje:EN
Publicado: Dove Medical Press 2017
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spelling oai:doaj.org-article:8b09564257c546a59438a0c394a77c8c2021-12-02T06:51:19ZDiabetes and dyslipidemia: characterizing lipoprotein metabolism1178-7007https://doaj.org/article/8b09564257c546a59438a0c394a77c8c2017-07-01T00:00:00Zhttps://www.dovepress.com/diabetes-and-dyslipidemia-characterizing-lipoprotein-metabolism-peer-reviewed-article-DMSOhttps://doaj.org/toc/1178-7007GH Tomkin,1,2 D Owens1,2 1Diabetes Institute of Ireland, Beacon Hospital, 2Trinity College, University of Dublin, Dublin, Ireland Abstract: Premature atherosclerosis in diabetes accounts for much of the decreased life span. New treatments have reduced this risk considerably. This review explores the relationship among the disturbances in glucose, lipid, and bile salt metabolic pathways that occur in diabetes. In particular, excess nutrient intake and starvation have major metabolic effects, which have allowed us new insights into the disturbance that occurs in diabetes. Metabolic regulators such as the forkhead transcription factors, the farnesyl X transcription factors, and the fibroblast growth factors have become important players in our understanding of the dysregulation of metabolism in diabetes and overnutrition. The disturbed regulation of lipoprotein metabolism in both the intestine and the liver has been more clearly defined over the past few years, and the atherogenicity of the triglyceride-rich lipoproteins, and – in tandem – low levels of high-density lipoproteins, is seen now as very important. New information on the apolipoproteins that control lipoprotein lipase activity has been obtained. This is an exciting time in the battle to defeat diabetic atherosclerosis. Keywords: obesity, type 2 diabetes, dyslipidemia, low-density lipoprotein, fibroblast growth factor, forkhead transcription factor O1, farnesyl X transcription factors Tomkin GHOwens DDove Medical PressarticleObesitytype 2 diabetesdyslipidaemialow density lipoprotein LDLfibroblast growth (factor FGF) forkhead transcription factor (FOX)O1farnesyl X transcription factors (FRX)Specialties of internal medicineRC581-951ENDiabetes, Metabolic Syndrome and Obesity: Targets and Therapy, Vol Volume 10, Pp 333-343 (2017)
institution DOAJ
collection DOAJ
language EN
topic Obesity
type 2 diabetes
dyslipidaemia
low density lipoprotein LDL
fibroblast growth (factor FGF) forkhead transcription factor (FOX)O1
farnesyl X transcription factors (FRX)
Specialties of internal medicine
RC581-951
spellingShingle Obesity
type 2 diabetes
dyslipidaemia
low density lipoprotein LDL
fibroblast growth (factor FGF) forkhead transcription factor (FOX)O1
farnesyl X transcription factors (FRX)
Specialties of internal medicine
RC581-951
Tomkin GH
Owens D
Diabetes and dyslipidemia: characterizing lipoprotein metabolism
description GH Tomkin,1,2 D Owens1,2 1Diabetes Institute of Ireland, Beacon Hospital, 2Trinity College, University of Dublin, Dublin, Ireland Abstract: Premature atherosclerosis in diabetes accounts for much of the decreased life span. New treatments have reduced this risk considerably. This review explores the relationship among the disturbances in glucose, lipid, and bile salt metabolic pathways that occur in diabetes. In particular, excess nutrient intake and starvation have major metabolic effects, which have allowed us new insights into the disturbance that occurs in diabetes. Metabolic regulators such as the forkhead transcription factors, the farnesyl X transcription factors, and the fibroblast growth factors have become important players in our understanding of the dysregulation of metabolism in diabetes and overnutrition. The disturbed regulation of lipoprotein metabolism in both the intestine and the liver has been more clearly defined over the past few years, and the atherogenicity of the triglyceride-rich lipoproteins, and – in tandem – low levels of high-density lipoproteins, is seen now as very important. New information on the apolipoproteins that control lipoprotein lipase activity has been obtained. This is an exciting time in the battle to defeat diabetic atherosclerosis. Keywords: obesity, type 2 diabetes, dyslipidemia, low-density lipoprotein, fibroblast growth factor, forkhead transcription factor O1, farnesyl X transcription factors 
format article
author Tomkin GH
Owens D
author_facet Tomkin GH
Owens D
author_sort Tomkin GH
title Diabetes and dyslipidemia: characterizing lipoprotein metabolism
title_short Diabetes and dyslipidemia: characterizing lipoprotein metabolism
title_full Diabetes and dyslipidemia: characterizing lipoprotein metabolism
title_fullStr Diabetes and dyslipidemia: characterizing lipoprotein metabolism
title_full_unstemmed Diabetes and dyslipidemia: characterizing lipoprotein metabolism
title_sort diabetes and dyslipidemia: characterizing lipoprotein metabolism
publisher Dove Medical Press
publishDate 2017
url https://doaj.org/article/8b09564257c546a59438a0c394a77c8c
work_keys_str_mv AT tomkingh diabetesanddyslipidemiacharacterizinglipoproteinmetabolism
AT owensd diabetesanddyslipidemiacharacterizinglipoproteinmetabolism
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