Vapnik Joshua S, Kim Joon Bum, Isselbacher Eric M, Ghoshhajra Brian B, Cheng Yisha, Sundt Thoralf M, MacGillivray Thomas E, Cambria Richard P, Lindsay Mark E
Massachusetts General Hospital Thoracic Aortic Center, Harvard Medical School, Boston, Massachusetts; Division of Cardiology, Harvard Medical School, Boston, Massachusetts.
Massachusetts General Hospital Thoracic Aortic Center, Harvard Medical School, Boston, Massachusetts; Division of Cardiac Surgery, Harvard Medical School, Boston, Massachusetts; Department of Thoracic and Cardiovascular Surgery, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea.
Am J Cardiol. 2016 May 15;117(10):1683-1690. doi: 10.1016/j.amjcard.2016.02.048. Epub 2016 Mar 2.
Thoracic aortic aneurysms (TAs) occur in reproducible patterns, but etiologic factors determining the anatomic distribution of these aneurysms are not well understood. This study sought to gain insight into etiologic differences and clinical outcomes associated with repetitive anatomic distributions of TAs. From 3,247 patients registered in an institutional Thoracic Aortic Center database from July 1992 to August 2013, we identified 844 patients with full aortic dimensional imaging by computerized axial tomography or magnetic resonance imaging scan (mean age 62.8 ± 14 years, 37% women, median follow-up 40 months) with TA diameter >4.0 cm and without evidence of previous aortic dissection. Patient demographic and imaging data were analyzed in 3 groups: isolated ascending thoracic aortic aneurysms (AAs; n = 628), isolated descending TAs (DTAs; n = 130), and combined AA and DTA (mixed thoracic aortic aneurysm, MTA; n = 86). Patients with DTA had more hypertension (82% vs 59%, p <0.001) and a higher burden of atherosclerosis (88% vs 9%, p <0.001) than AA. Conversely, patients with isolated AA were younger (59.5 ± 13.5 vs 71.0 ± 11.8 years, p <0.001) and contained almost every case of overt, genetically triggered TA. Patients with isolated DTA were demographically indistinguishable from patients with MTA. In follow-up, patients with DTA/MTA experienced more aortic events (aortic dissection/rupture) and had higher mortality than patients with isolated AA. In multivariate analysis, aneurysm size (odds ratio 1.1, 95% CI 1.07 to 1.16, p <0.001) and the presence of atherosclerosis (odds ratio 5.7, 95% CI 2.02 to 16.15, p <0.001) independently predicted adverse aortic events. We find that DTA with or without associated AA appears to be a disease more highly associated with atherosclerosis, hypertension, and advanced age. In contrast, isolated AA appears to be a clinically distinct entity with a greater burden of genetically triggered disease.
胸主动脉瘤(TA)以可重复的模式出现,但决定这些动脉瘤解剖分布的病因因素尚未完全明确。本研究旨在深入了解与TA重复解剖分布相关的病因差异和临床结果。在1992年7月至2013年8月登记在一个机构胸主动脉中心数据库中的3247例患者中,我们通过计算机断层扫描或磁共振成像扫描确定了844例有完整主动脉尺寸成像的患者(平均年龄62.8±14岁,女性占37%,中位随访时间40个月),这些患者的TA直径>4.0 cm且无既往主动脉夹层的证据。患者的人口统计学和成像数据被分为3组进行分析:孤立性升胸主动脉瘤(AA;n = 628)、孤立性降胸主动脉瘤(DTA;n = 130)以及AA和DTA合并存在(混合性胸主动脉瘤,MTA;n = 86)。与AA患者相比,DTA患者有更多的高血压(82%对59%,p<0.001)和更高的动脉粥样硬化负担(88%对9%,p<0.001)。相反,孤立性AA患者更年轻(59.5±13.5岁对71.0±11.8岁,p<0.001),且几乎包含了所有明显的、由基因引发的TA病例。孤立性DTA患者在人口统计学上与MTA患者无差异。在随访中,DTA/MTA患者经历了更多的主动脉事件(主动脉夹层/破裂),且死亡率高于孤立性AA患者。在多变量分析中,动脉瘤大小(比值比1.1,95%置信区间1.07至1.16,p<0.001)和动脉粥样硬化的存在(比值比5.7,95%置信区间2.02至16.15,p<0.001)独立预测不良主动脉事件。我们发现,伴有或不伴有相关AA的DTA似乎是一种与动脉粥样硬化、高血压和高龄更高度相关的疾病。相比之下,孤立性AA似乎是一个临床上独特的实体,有更大的基因引发疾病负担。