Berardi Cecilia, Wassel Christine L, Decker Paul A, Larson Nicholas B, Kirsch Phillip S, Andrade Mariza de, Tsai Michael Y, Pankow James S, Sale Michele M, Sicotte Hugues, Tang Weihong, Hanson Naomi Q, McDermott Mary M, Criqui Michael H, Allison Michael A, Bielinski Suzette J
1 Department of Internal Medicine, Albert Einstein College of Medicine and Montefiore Medical Center, Bronx, NY, USA.
2 Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Angiology. 2017 Apr;68(4):322-329. doi: 10.1177/0003319716659178. Epub 2016 Jul 20.
Inflammation plays a pivotal role in peripheral artery disease (PAD). Cellular adhesion proteins mediate the interaction of leukocytes with endothelial cells during inflammation. To determine the association of cellular adhesion molecules with ankle-brachial index (ABI) and ABI category (≤1.0 vs >1.0) in a diverse population, 15 adhesion proteins were measured in the Multi-Ethnic Study of Atherosclerosis (MESA). To assess multivariable associations of each protein with ABI and ABI category, linear and logistic regression was used, respectively. Among 2364 participants, 23 presented with poorly compressible arteries (ABI > 1.4) and were excluded and 261 had ABI ≤ 1.0. Adjusting for traditional risk factors, elevated levels of soluble P-selectin, hepatocyte growth factor, and secretory leukocyte protease inhibitor were associated with lower ABI ( P = .0004, .001, and .002, respectively). Per each standard deviation of protein, we found 26%, 20%, and 19% greater odds of lower ABI category ( P = .001, .01, and .02, respectively). Further investigation into the adhesion pathway may shed new light on biological mechanisms implicated in PAD.
炎症在周围动脉疾病(PAD)中起关键作用。细胞黏附蛋白在炎症过程中介导白细胞与内皮细胞的相互作用。为了确定细胞黏附分子与不同人群中踝臂指数(ABI)及ABI类别(≤1.0与>1.0)之间的关联,在动脉粥样硬化多民族研究(MESA)中检测了15种黏附蛋白。为评估每种蛋白与ABI及ABI类别的多变量关联,分别使用了线性回归和逻辑回归。在2364名参与者中,23人动脉难以压缩(ABI>1.4)被排除,261人ABI≤1.0。在调整传统风险因素后,可溶性P选择素、肝细胞生长因子和分泌型白细胞蛋白酶抑制剂水平升高与较低的ABI相关(分别为P = .0004、.001和.002)。蛋白每增加一个标准差,我们发现ABI类别较低的几率分别增加26%、20%和19%(分别为P = .001、.01和.02)。对黏附途径的进一步研究可能会为PAD涉及的生物学机制带来新的启示。