4.4 Review

Current Theories and Clinical Trial Evidence for Limiting Human Abdominal Aortic Aneurysm Growth

期刊

CURRENT DRUG TARGETS
卷 19, 期 11, 页码 1302-1308

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1389450118666171113114310

关键词

Abdominal aortic aneurysm; pathogenesis; drug intervention; clinical trials; doxycycline; atorvastatin; telmisartan

资金

  1. Key Program of Hunan Provincial Department of Science and Technology [2015SK2017]
  2. Clinical Research Project of Xiangya Hospital, CSU
  3. Scientific Research Foundation for Returned Overseas Chinese Scholars, State Education Ministry

向作者/读者索取更多资源

Background: Abdominal aortic aneurysm (AAA) refers to localized dilation of abdominal aorta. AAA is largely asymptomatic, but aneurysmal rupture results in a high mortality rate. AAA with a diameter greater than 55 mm carries a high risk of rupture. There are currently no known medical treatments effective in limiting the growth of small AAA. Objective: To review the current status of and challenges faced in limiting AAA growth. Methods: Data from human investigations and animal model studies were summarized. In particular, the ClinicalTrials.gov website was searched for details of ongoing or completed studies related to AAA growth. We searched the key words 'abdominal aortic aneurysm' and 'drugs' to identify potential target drugs for slowing or stopping AAA growth. Results: These clinical trials involve a number of challenges, including demonstrating the design of the trial, minimizing the participant dropout rate, and developing accurate outcome assessments during the trials. A number of clinical trials have concentrated on pharmaceutical intervention (such as angiotensin-converting enzyme inhibitors, beta-blockers, statins, and antibiotics) that could be effective for AAA patients in delaying or reversing aneurysm expansion and postponing the endpoint for elective surgical repair. Conclusions: Further randomized, controlled, clinical trials are required to develop effective nonsurgical therapies for AAA.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据