Relation of Aortic Stiffness to Left Ventricular Remodeling in Younger Adults With Type 2 Diabetes

Individuals with type 2 diabetes have a three- to fivefold increased risk of developing heart failure. Diabetic cardiomyopathy is typified by left ventricular (LV) concentric remodeling, which is a recognized predictor of adverse cardiovascular events. Although the mechanisms underlying LV remodelin...

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Published inDiabetes (New York, N.Y.) Vol. 67; no. 7; pp. 1395 - 1400
Main Authors Gulsin, Gaurav S, Swarbrick, Daniel J, Hunt, William H, Levelt, Eylem, Graham-Brown, Matthew P M, Parke, Kelly S, Wormleighton, Joanne V, Lai, Florence Y, Yates, Thomas, Wilmot, Emma G, Webb, David R, Davies, Melanie J, McCann, Gerry P
Format Journal Article
LanguageEnglish
Published United States American Diabetes Association 01.07.2018
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Abstract Individuals with type 2 diabetes have a three- to fivefold increased risk of developing heart failure. Diabetic cardiomyopathy is typified by left ventricular (LV) concentric remodeling, which is a recognized predictor of adverse cardiovascular events. Although the mechanisms underlying LV remodeling in type 2 diabetes are unclear, progressive aortic stiffening may be a key determinant. The aim of this study was to assess the relationship between aortic stiffness and LV geometry in younger adults with type 2 diabetes, using multiparametric cardiovascular MRI. We prospectively recruited 80 adults (aged 18-65 years) with type 2 diabetes and no cardiovascular disease and 20 age- and sex-matched healthy control subjects. All subjects underwent comprehensive bio-anthropometric assessment and cardiac MRI, including measurement of aortic stiffness by aortic distensibility (AD). Type 2 diabetes was associated with increased LV mass, concentric LV remodeling, and lower AD compared with control subjects. On multivariable linear regression, AD was independently associated with concentric LV remodeling in type 2 diabetes. Aortic stiffness may therefore be a potential therapeutic target to prevent the development of heart failure in type 2 diabetes.
AbstractList Individuals with type 2 diabetes have a three- to fivefold increased risk of developing heart failure. Diabetic cardiomyopathy is typified by left ventricular (LV) concentric remodeling, which is a recognized predictor of adverse cardiovascular events. Although the mechanisms underlying LV remodeling in type 2 diabetes are unclear, progressive aortic stiffening may be a key determinant. The aim of this study was to assess the relationship between aortic stiffness and LV geometry in younger adults with type 2 diabetes, using multiparametric cardiovascular MRI. We prospectively recruited 80 adults (aged 18-65 years) with type 2 diabetes and no cardiovascular disease and 20 age- and sex-matched healthy control subjects. All subjects underwent comprehensive bio-anthropometric assessment and cardiac MRI, including measurement of aortic stiffness by aortic distensibility (AD). Type 2 diabetes was associated with increased LV mass, concentric LV remodeling, and lower AD compared with control subjects. On multivariable linear regression, AD was independently associated with concentric LV remodeling in type 2 diabetes. Aortic stiffness may therefore be a potential therapeutic target to prevent the development of heart failure in type 2 diabetes.
Author Levelt, Eylem
Swarbrick, Daniel J
Yates, Thomas
Lai, Florence Y
Webb, David R
McCann, Gerry P
Gulsin, Gaurav S
Graham-Brown, Matthew P M
Parke, Kelly S
Wormleighton, Joanne V
Davies, Melanie J
Wilmot, Emma G
Hunt, William H
Author_xml – sequence: 1
  givenname: Gaurav S
  orcidid: 0000-0002-1740-9270
  surname: Gulsin
  fullname: Gulsin, Gaurav S
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
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  givenname: Daniel J
  surname: Swarbrick
  fullname: Swarbrick, Daniel J
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
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  givenname: William H
  surname: Hunt
  fullname: Hunt, William H
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
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  givenname: Eylem
  surname: Levelt
  fullname: Levelt, Eylem
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
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  givenname: Matthew P M
  surname: Graham-Brown
  fullname: Graham-Brown, Matthew P M
  organization: National Centre of Sport and Exercise Medicine, University of Loughborough, Loughborough, U.K
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  givenname: Kelly S
  surname: Parke
  fullname: Parke, Kelly S
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
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  givenname: Joanne V
  surname: Wormleighton
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  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
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  givenname: Florence Y
  surname: Lai
  fullname: Lai, Florence Y
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K
– sequence: 9
  givenname: Thomas
  surname: Yates
  fullname: Yates, Thomas
  organization: National Centre of Sport and Exercise Medicine, University of Loughborough, Loughborough, U.K
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  givenname: Emma G
  surname: Wilmot
  fullname: Wilmot, Emma G
  organization: Department of Endocrinology and Diabetes, Royal Derby Hospital, Derby, U.K
– sequence: 11
  givenname: David R
  surname: Webb
  fullname: Webb, David R
  organization: Diabetes Research Centre, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Leicester General Hospital, Leicester, U.K
– sequence: 12
  givenname: Melanie J
  surname: Davies
  fullname: Davies, Melanie J
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  givenname: Gerry P
  surname: McCann
  fullname: McCann, Gerry P
  email: gpm12@leicester.ac.uk
  organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K. gpm12@leicester.ac.uk
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Snippet Individuals with type 2 diabetes have a three- to fivefold increased risk of developing heart failure. Diabetic cardiomyopathy is typified by left ventricular...
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StartPage 1395
SubjectTerms Adolescent
Adult
Aged
Aorta
Aortic Diseases - diagnosis
Aortic Diseases - epidemiology
Aortic Diseases - etiology
Aortic Diseases - physiopathology
Cardiomyopathy
Cardiovascular diseases
Case-Control Studies
Coronary vessels
Diabetes
Diabetes mellitus
Diabetes mellitus (non-insulin dependent)
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - diagnosis
Diabetes Mellitus, Type 2 - epidemiology
Diabetes Mellitus, Type 2 - physiopathology
Diabetic Cardiomyopathies - diagnosis
Diabetic Cardiomyopathies - epidemiology
Diabetic Cardiomyopathies - physiopathology
Female
Heart diseases
Heart failure
Humans
Hypertrophy, Left Ventricular - complications
Hypertrophy, Left Ventricular - diagnosis
Hypertrophy, Left Ventricular - epidemiology
Magnetic Resonance Imaging
Male
Middle Aged
NMR
Nuclear magnetic resonance
Risk Factors
Therapeutic applications
Vascular Stiffness - physiology
Ventricle
Ventricular Remodeling - physiology
Young Adult
Young adults
Title Relation of Aortic Stiffness to Left Ventricular Remodeling in Younger Adults With Type 2 Diabetes
URI https://www.ncbi.nlm.nih.gov/pubmed/29661781
https://www.proquest.com/docview/2089728601
https://search.proquest.com/docview/2026422892
Volume 67
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