Literature DB >> 24913570

Long-term renin-angiotensin blocking therapy in hypertensive patients with normal aorta may attenuate the formation of abdominal aortic aneurysms.

Daniel Silverberg1, Anan Younis2, Naphtali Savion3, Gil Harari4, Dmitry Yakubovitch1, Basheer Sheick Yousif1, Moshe Halak1, Ehud Grossman2, Jacob Schneiderman5.   

Abstract

Renin-angiotensin system (RAS) has been implicated in the pathogenesis of abdominal aortic aneurysm (AAA). Angiotensin II type 1 receptor blocker (ARB), when given with angiotensin II prevents AAA formation in mice, but found ineffective in attenuating the progression of preexisting AAA. This study was designed to evaluate the effect of chronic RAS blockers on abdominal aortic diameter in hypertensive patients without known aortic aneurysm. Consecutive hypertensive outpatients (n = 122) were stratified according to antihypertensive therapy they received for 12 months or more, consisting of ARB (n = 45), angiotensin converting enzyme inhibitor (ACE-I; n = 45), or nonARB/nonACE-I (control therapy; n = 32). Abdominal ultrasonography was performed to measure maximal subrenal aortic diameter. Eighty-four patients were reexamined by ultrasonography 8 months later. The correlation between the different antihypertensive therapies and aortic diameter was examined. Aortic diameters were significantly smaller in ARB than in control patients in the baseline and follow-up measurements (P = .004; P = .0004, respectively). Risk factor adjusted covariance analysis showed significant differences between ARB or ACE-I treated groups and controls (P = .006 or P = .046, respectively). Ultrasound that was performed 8 months later showed smaller increases in mean aortic diameters of the ARB and ACE-I groups than in controls. Both ARB and ACE-I therapy attenuated expansion of nonaneurysmal abdominal aorta in humans. These results indicate that RAS blockade given before advancement of aortic medial remodeling may slow down the development of AAA.
Copyright © 2014 American Society of Hypertension. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Angiotensin II; leptin; vascular remodeling

Mesh:

Substances:

Year:  2014        PMID: 24913570     DOI: 10.1016/j.jash.2014.04.005

Source DB:  PubMed          Journal:  J Am Soc Hypertens        ISSN: 1878-7436


  5 in total

1.  Angiotensin-converting enzyme 2 decreases formation and severity of angiotensin II-induced abdominal aortic aneurysms.

Authors:  Sean E Thatcher; Xuan Zhang; Deborah A Howatt; Frederique Yiannikouris; Susan B Gurley; Terri Ennis; John A Curci; Alan Daugherty; Lisa A Cassis
Journal:  Arterioscler Thromb Vasc Biol       Date:  2014-10-09       Impact factor: 8.311

Review 2.  Decoding inflammation, its causes, genomic responses, and emerging countermeasures.

Authors:  Jacek Hawiger; Jozef Zienkiewicz
Journal:  Scand J Immunol       Date:  2019-08-28       Impact factor: 3.487

Review 3.  Angiotensin-converting enzyme 2, coronavirus disease 2019, and abdominal aortic aneurysms.

Authors:  Baohui Xu; Gang Li; Jia Guo; Toru Ikezoe; Karthikeshwar Kasirajan; Sihai Zhao; Ronald L Dalman
Journal:  J Vasc Surg       Date:  2021-02-15       Impact factor: 4.268

4.  Large-Conductance Calcium-Activated Potassium Channel Opener, NS1619, Protects Against Mesenteric Artery Remodeling Induced by Agonistic Autoantibodies Against the Angiotensin II Type 1 Receptor.

Authors:  Meili Wang; Xiaochen Yin; Shuanglei Li; Xi Zhang; Ming Yi; Chunyu He; Xiaoyue Li; Wei Wang; Suli Zhang; Huirong Liu
Journal:  J Am Heart Assoc       Date:  2022-02-12       Impact factor: 6.106

5.  Local Application of Leptin Antagonist Attenuates Angiotensin II-Induced Ascending Aortic Aneurysm and Cardiac Remodeling.

Authors:  Danny Ben-Zvi; Naphtali Savion; Frank Kolodgie; Amos Simon; Sudeshna Fisch; Katrin Schäfer; Noa Bachner-Hinenzon; Xin Cao; Arieh Gertler; Gili Solomon; Erez Kachel; Ehud Raanani; Jacob Lavee; Shlomo Kotev Emeth; Renu Virmani; Frederick J Schoen; Jacob Schneiderman
Journal:  J Am Heart Assoc       Date:  2016-05-03       Impact factor: 5.501

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.