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Comprehensive characterisation of hypertensive heart disease left ventricular phenotypes.
Rodrigues, Jonathan C L; Amadu, Antonio Matteo; Dastidar, Amardeep Ghosh; Szantho, Gergley V; Lyen, Stephen M; Godsave, Cattleya; Ratcliffe, Laura E K; Burchell, Amy E; Hart, Emma C; Hamilton, Mark C K; Nightingale, Angus K; Paton, Julian F R; Manghat, Nathan E; Bucciarelli-Ducci, Chiara.
Afiliação
  • Rodrigues JC; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK School of Physiology, Pharmacology and Neurosciences, Faculty of Biomedical Sciences, University of Bristol, University
  • Amadu AM; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK Department of Surgical, Microsurgical and Medical Sciences, Institute of Radiology, University of Sassari, Sassari, Pia
  • Dastidar AG; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK Department of Cardiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Szantho GV; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK Department of Cardiology, University Hospital of Wales, Cardiff.
  • Lyen SM; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK Department of Clinical Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol,
  • Godsave C; Department of General Medicine, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Ratcliffe LE; CardioNomics Research Group, Clinical Research Imaging Centre (CRIC) Bristol, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Burchell AE; Department of Cardiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, UK CardioNomics Research Group, Clinical Research Imaging Centre (CRIC) Bristol, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Hart EC; School of Physiology, Pharmacology and Neurosciences, Faculty of Biomedical Sciences, University of Bristol, University Walk, Bristol, UK CardioNomics Research Group, Clinical Research Imaging Centre (CRIC) Bristol, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol,
  • Hamilton MC; Department of Clinical Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Nightingale AK; Department of Cardiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, UK CardioNomics Research Group, Clinical Research Imaging Centre (CRIC) Bristol, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Paton JF; School of Physiology, Pharmacology and Neurosciences, Faculty of Biomedical Sciences, University of Bristol, University Walk, Bristol, UK CardioNomics Research Group, Clinical Research Imaging Centre (CRIC) Bristol, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol,
  • Manghat NE; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK Department of Clinical Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol,
  • Bucciarelli-Ducci C; NIHR Bristol Cardiovascular Biomedical Research Unit, Cardiac Magnetic Resonance Department, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, UK Department of Cardiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
Heart ; 102(20): 1671-9, 2016 10 15.
Article em En | MEDLINE | ID: mdl-27260191
ABSTRACT

OBJECTIVE:

Myocardial intracellular/extracellular structure and aortic function were assessed among hypertensive left ventricular (LV) phenotypes using cardiovascular magnetic resonance (CMR).

METHODS:

An observational study from consecutive tertiary hypertension clinic patients referred for CMR (1.5 T) was performed. Four LV phenotypes were defined (1) normal with normal indexed LV mass (LVM) and LVM to volume ratio (M/V), (2) concentric remodelling with normal LVM but elevated M/V, (3) concentric LV hypertrophy (LVH) with elevated LVM but normal indexed end-diastolic volume (EDV) or (4) eccentric LVH with elevated LVM and EDV. Extracellular volume fraction was measured using T1-mapping. Circumferential strain was calculated by voxel-tracking. Aortic distensibility was derived from high-resolution aortic cines and contemporaneous blood pressure measurements.

RESULTS:

88 hypertensive patients (49±14 years, 57% men, systolic blood pressure (SBP) 167±30 mm Hg, diastolic blood pressure (DBP) 96±14 mm Hg) were compared with 29 age-matched/sex-matched controls (47±14 years, 59% men, SBP 128±12 mm Hg, DBP 79±10 mm Hg). LVH resulted from increased myocardial cell volume (eccentric LVH 78±19 mL/m(2) vs concentric LVH 73±15 mL/m(2) vs concentric remodelling 55±9 mL/m(2), p<0.05, respectively) and interstitial fibrosis (eccentric LVH 33±10 mL/m(2) vs concentric LVH 30±10 mL/m(2) vs concentricremodelling 19±2 mL/m(2), p<0.05, respectively). LVH had worst circumferential impairment (eccentric LVH -12.8±4.6% vs concentric LVH -15.5±3.1% vs concentric remodelling -17.1±3.2%, p<0.05, respectively). Concentric remodelling was associated with reduced aortic distensibility, but not with large intracellular/interstitial expansion or myocardial dysfunction versus controls.

CONCLUSIONS:

Myocardial interstitial fibrosis varies across hypertensive LV phenotypes with functional consequences. Eccentric LVH has the most fibrosis and systolic impairment. Concentric remodelling is only associated with abnormal aortic function. Understanding these differences may help tailor future antihypertensive treatments.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Função Ventricular Esquerda / Hipertrofia Ventricular Esquerda / Disfunção Ventricular Esquerda / Imagem Cinética por Ressonância Magnética / Hipertensão / Miocárdio Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Função Ventricular Esquerda / Hipertrofia Ventricular Esquerda / Disfunção Ventricular Esquerda / Imagem Cinética por Ressonância Magnética / Hipertensão / Miocárdio Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Ano de publicação: 2016 Tipo de documento: Article