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 in | Diabetes (New York, N.Y.) Vol. 67; no. 7; pp. 1395 - 1400 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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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. |
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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 – sequence: 2 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 – sequence: 3 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 – sequence: 4 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 – sequence: 5 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 – sequence: 6 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 – sequence: 7 givenname: Joanne V surname: Wormleighton fullname: Wormleighton, Joanne V organization: Department of Cardiovascular Sciences, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Glenfield Hospital, Leicester, U.K – sequence: 8 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 – sequence: 10 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 organization: Diabetes Research Centre, University of Leicester and Leicester National Institute for Health Research Biomedical Research Centre, Leicester General Hospital, Leicester, U.K – sequence: 13 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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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 |
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