医学
马凡氏综合征
腹主动脉瘤
动脉瘤
临床试验
主动脉瘤
背景(考古学)
腹主动脉
主动脉
疾病
病态的
重症监护医学
外科
放射科
心脏病学
内科学
古生物学
生物
作者
J. Lindeman,Jon S. Matsumura
出处
期刊:Circulation Research
[Ovid Technologies (Wolters Kluwer)]
日期:2019-02-15
卷期号:124 (4): 631-646
被引量:86
标识
DOI:10.1161/circresaha.118.312439
摘要
Current management of aortic aneurysms relies exclusively on prophylactic operative repair of larger aneurysms. Great potential exists for successful medical therapy that halts or reduces aneurysm progression and hence alleviates or postpones the need for surgical repair. Preclinical studies in the context of abdominal aortic aneurysm identified hundreds of candidate strategies for stabilization, and data from preoperative clinical intervention studies show that interventions in the pathways of the activated inflammatory and proteolytic cascades in enlarging abdominal aortic aneurysm are feasible. Similarly, the concept of pharmaceutical aorta stabilization in Marfan syndrome is supported by a wealth of promising studies in the murine models of Marfan syndrome–related aortapathy. Although some clinical studies report successful medical stabilization of growing aortic aneurysms and aortic root stabilization in Marfan syndrome, these claims are not consistently confirmed in larger and controlled studies. Consequently, no medical therapy can be recommended for the stabilization of aortic aneurysms. The discrepancy between preclinical successes and clinical trial failures implies shortcomings in the available models of aneurysm disease and perhaps incomplete understanding of the pathological processes involved in later stages of aortic aneurysm progression. Preclinical models more reflective of human pathophysiology, identification of biomarkers to predict severity of disease progression, and improved design of clinical trials may more rapidly advance the opportunities in this important field.
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