Kim Ha Won, Stansfield Brian K
Vascular Biology Center, Augusta University, Augusta, GA, USA.
Vascular Biology Center, Augusta University, Augusta, GA, USA; Department of Pediatrics, Medical College of Georgia, Augusta University, Augusta, GA, USA.
Biomed Res Int. 2017;2017:7268521. doi: 10.1155/2017/7268521. Epub 2017 Jan 1.
Aneurysms are characterized by structural deterioration of the vascular wall leading to progressive dilatation and, potentially, rupture of the aorta. While aortic aneurysms often remain clinically silent, the morbidity and mortality associated with aneurysm expansion and rupture are considerable. Over 13,000 deaths annually in the United States are attributable to aortic aneurysm rupture with less than 1 in 3 persons with aortic aneurysm rupture surviving to surgical intervention. Environmental and epidemiologic risk factors including smoking, male gender, hypertension, older age, dyslipidemia, atherosclerosis, and family history are highly associated with abdominal aortic aneurysms, while heritable genetic mutations are commonly associated with aneurysms of the thoracic aorta. Similar to other forms of cardiovascular disease, family history, genetic variation, and heritable mutations modify the risk of aortic aneurysm formation and provide mechanistic insight into the pathogenesis of human aortic aneurysms. This review will examine the relationship between heritable genetic and epigenetic influences on thoracic and abdominal aortic aneurysm formation and rupture.
动脉瘤的特征是血管壁结构恶化,导致主动脉逐渐扩张,并可能破裂。虽然主动脉瘤在临床上通常没有症状,但与动脉瘤扩张和破裂相关的发病率和死亡率相当高。在美国,每年有超过13000人死于主动脉瘤破裂,主动脉瘤破裂患者中不到三分之一能存活到接受手术干预。环境和流行病学风险因素,包括吸烟、男性、高血压、老年、血脂异常、动脉粥样硬化和家族史,与腹主动脉瘤高度相关,而遗传性基因突变通常与胸主动脉瘤相关。与其他形式的心血管疾病类似,家族史、基因变异和遗传性突变会改变主动脉瘤形成的风险,并为人类主动脉瘤的发病机制提供机制性见解。本综述将探讨遗传性基因和表观遗传影响与胸主动脉瘤和腹主动脉瘤形成及破裂之间的关系。