AI Article Synopsis

  • * A study in the Multi-Ethnic Study of Atherosclerosis (MESA) analyzed 15 adhesion proteins in 2,364 participants to determine their relationship with the ankle-brachial index (ABI), a measure of arterial health.
  • * Findings revealed that higher levels of certain proteins (soluble P-selectin, hepatocyte growth factor, secretory leukocyte protease inhibitor) were linked to lower ABI, suggesting that these proteins could be important in understanding PAD's biological mechanisms.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5247409PMC
http://dx.doi.org/10.1177/0003319716659178DOI Listing

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