CAPITAL Research Group Division of Cardiology University of Ottawa Heart Institute Ottawa Canada.
Department of Cellular and Molecular Medicine University of Ottawa Canada.
J Am Heart Assoc. 2019 Aug 6;8(15):e012228. doi: 10.1161/JAHA.119.012228. Epub 2019 Aug 5.
Background Adenosine is a ubiquitous regulatory molecule known to modulate signaling in many cells and processes vital to vascular homeostasis. While studies of adenosine receptors have dominated research in the field, quantification of adenosine systemically and locally remains limited owing largely to technical restrictions. Given the potential clinical implications of adenosine biology, there is a need for adequately powered studies examining the role of plasma adenosine in vascular health. We sought to describe the analytical and biological factors that affect quantification of adenosine in humans in a large, real-world cohort of patients undergoing evaluation for coronary artery disease. Methods and Results Between November 2016 and April 2018, we assessed 1141 patients undergoing angiography for evaluation of coronary artery disease. High-performance liquid chromatography was used for quantification of plasma adenosine concentration, yielding an analytical coefficient of variance (CV) of 3.2%, intra-subject variance (CV) 35.8% and inter-subject variance (CV) 56.7%. Traditional cardiovascular risk factors, medications, and clinical presentation had no significant impact on adenosine levels. Conversely, increasing age (P=0.027) and the presence of obstructive coronary artery disease (P=0.026) were associated with lower adenosine levels. Adjusted multivariable analysis supported only age being inversely associated with adenosine levels (P=0.039). Conclusions Plasma adenosine is not significantly impacted by traditional cardiovascular risk factors; however, advancing age and presence of obstructive coronary artery disease may be associated with lower adenosine levels. The degree of intra- and inter-subject variance of adenosine has important implications for biomarker use as a prognosticator of cardiovascular outcomes and as an end point in clinical studies.
腺苷是一种普遍存在的调节分子,已知可调节许多细胞和对血管稳态至关重要的过程中的信号转导。虽然腺苷受体的研究主导了该领域的研究,但由于技术限制,系统和局部腺苷系统的定量仍然有限。鉴于腺苷生物学的潜在临床意义,需要进行充分的研究,以检验血浆腺苷在血管健康中的作用。我们旨在描述影响人类腺苷定量的分析和生物学因素,该研究基于一个接受冠状动脉疾病评估的大型真实世界患者队列。
在 2016 年 11 月至 2018 年 4 月期间,我们评估了 1141 例接受血管造影术以评估冠状动脉疾病的患者。高效液相色谱法用于定量血浆腺苷浓度,得出分析变异系数(CV)为 3.2%,个体内 CV 为 35.8%,个体间 CV 为 56.7%。传统心血管危险因素、药物和临床表现对腺苷水平没有显著影响。相反,年龄增加(P=0.027)和存在阻塞性冠状动脉疾病(P=0.026)与较低的腺苷水平相关。调整后的多变量分析仅支持年龄与腺苷水平呈负相关(P=0.039)。
血浆腺苷不受传统心血管危险因素的显著影响;然而,年龄增长和阻塞性冠状动脉疾病的存在可能与较低的腺苷水平相关。腺苷的个体内和个体间变异程度对生物标志物的应用具有重要意义,可作为心血管结局的预测因子和临床研究的终点。