Endovascular reversal of renovascular hypertension blunts cardiac dysfunction and deformation in swine.


Journal

Journal of hypertension
ISSN: 1473-5598
Titre abrégé: J Hypertens
Pays: Netherlands
ID NLM: 8306882

Informations de publication

Date de publication:
01 03 2021
Historique:
pubmed: 6 1 2021
medline: 16 10 2021
entrez: 5 1 2021
Statut: ppublish

Résumé

Renovascular hypertension (RVH) induces hemodynamic and humoral aberrations that may impair cardiac function, structure and mechanics, including cardiac twist and deformation. Revascularization of a stenotic renal artery can decrease blood pressure (BP), but its ability to restore cardiac mechanics in RVH remains unclear. We hypothesized that percutaneous transluminal renal angioplasty (PTRA) would improve cardiac function and left ventricular (LV) deformation in swine RVH. Seventeen domestic pigs were studied for 16 weeks: RVH, RVH + PTRA and normal controls (n = 5-6 each). Global LV function was estimated by multidetector computed-tomography, and LV deformation by electrocardiographically triggered MRI tagging at the apical, mid, and basal LV levels. Cardiomyocyte hypertrophy, myocardial capillary density, and fibrosis were evaluated ex vivo. BP and wall thickness were elevated in RVH and decreased by PTRA, yet remained higher than in controls. LV myocardial muscle mass increased in RVH pigs, which also developed diastolic dysfunction, whereas cardiac output increased. Furthermore, both apical rotation and peak torsion angle increased in RVH compared with controls. Ex vivo, RVH induced myocardial fibrosis and vascular rarefaction. PTRA restored cardiac function and alleviated hypertrophy, vascular rarefaction, and fibrosis. PTRA also normalized apical rotation and peak torsion angle, and elevated basal peak radial strain and apical peak radial strain compared with RVH. In addition to cardiac LV adaptive hypertrophy and diastolic dysfunction, short-term RVH causes cardiac deformation. Despite only partial improvement in BP, PTRA effectively restored cardiac function and reversed abnormal mechanics. Hence, renal revascularization may be a useful strategy to preserve cardiac function in RVH.

Identifiants

pubmed: 33399301
doi: 10.1097/HJH.0000000000002654
pii: 00004872-202103000-00023
pmc: PMC8400925
mid: NIHMS1731048
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

556-562

Subventions

Organisme : NIDDK NIH HHS
ID : R01 DK122734
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK104273
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK102325
Pays : United States
Organisme : NIA NIH HHS
ID : R21 AG062104
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK120292
Pays : United States

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

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Auteurs

Shasha Yu (S)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Department of Cardiology, First Hospital of China Medical University, Shenyang, Liaoning, China.

Kai Jiang (K)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.

Xiang Y Zhu (XY)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.

Christopher M Ferguson (CM)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.

James D Krier (JD)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.

Amir Lerman (A)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.

Lilach O Lerman (LO)

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
Department of Cardiovascular Medicine, Mayo Clinic, Rochester, Minnesota, USA.

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