Barth Rolf F, Maximilian Buja L, Cao Lei, Brodsky Sergey V
Department of Pathology, The Ohio State University, 4132 Graves Hall, 333 W. 10th Ave, Columbus, OH, 43210, USA.
McGovern Medical School, Department of Pathology and Laboratory Medicine, University of Texas, 6431 Fannin St. MSB2.276, Houston, TX, 77030, USA.
Curr Hypertens Rep. 2017 Jul;19(7):55. doi: 10.1007/s11906-017-0753-y.
Brodsky et al. (Cardiovasc Pathol 25(6), 515-520, 2016) recently have reported that there was an unexpected and highly significant inverse correlation between body mass index (BMI) and atherosclerosis of the aortas of morbidly obese decedents (BMI >40 kg/m). In a series of 304 decedents, 65 of whom were morbidly obese, minimal or no atherosclerosis was seen in 46 of them (70%) versus 20 (30%) who had severe atherosclerosis (P = 0.008). This obesity paradox was unexpected and raises important questions about the etiology and pathogenesis of atherosclerosis, which will be the subject of this commentary. The concept of healthy versus unhealthy adiposity may in part provide an explanation for the "obesity paradox." Another factor that will be considered is the possible role of adipokines and their genetic determinants that may significantly reduce the risk of developing aortic atherosclerosis in morbidly obese individuals. Considering the marked variability in the pattern and extent of atherosclerosis of the aorta, hemodynamic factors and endothelial cell shear stress may be the most important determinants that might explain the obesity paradox that we have observed. Finally, the possible role of gut microbiota and inflammation as factors in the etiopathogenesis of atherosclerosis will be considered, but their importance is less clear than that of hemodynamic factors. We conclude with the remarkable finding that a 5300-year-old, well-preserved mummy of the "Iceman," Ötzi had atherosclerotic disease of a number of major arteries and the interesting questions that this raises.
布罗德斯基等人(《心血管病理学》25(6),515 - 520,2016年)最近报告称,在病态肥胖死者(体重指数>40 kg/m²)中,体重指数(BMI)与主动脉粥样硬化之间存在意外且高度显著的负相关。在一系列304名死者中,65名是病态肥胖者,其中46人(70%)可见极少或无动脉粥样硬化,而20人(30%)有严重动脉粥样硬化(P = 0.008)。这种肥胖悖论出人意料,引发了关于动脉粥样硬化病因和发病机制的重要问题,这将是本评论的主题。健康肥胖与不健康肥胖的概念可能部分解释了“肥胖悖论”。另一个将被考虑的因素是脂肪因子及其基因决定因素可能在显著降低病态肥胖个体发生主动脉粥样硬化风险方面所起的作用。考虑到主动脉粥样硬化的模式和程度存在显著差异,血流动力学因素和内皮细胞切应力可能是解释我们所观察到的肥胖悖论的最重要决定因素。最后,将考虑肠道微生物群和炎症在动脉粥样硬化病因发病机制中的可能作用,但其重要性不如血流动力学因素明确。我们以一个显著发现作为结论,即有5300年历史、保存完好的“冰人”奥茨木乃伊有许多主要动脉的动脉粥样硬化疾病,以及由此引发的有趣问题。