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血小板功能、动脉钙和血管功能测量的趋势。

Trends among platelet function, arterial calcium, and vascular function measures.

机构信息

National Heart, Lung and Blood Institute's the Framingham Heart Study, Boston University and National Heart, Framingham, MA, USA.

National Heart, Lung and Blood Institute, Population Sciences Branch, Framingham, MA, USA.

出版信息

Platelets. 2023 Dec;34(1):2238835. doi: 10.1080/09537104.2023.2238835.

DOI:10.1080/09537104.2023.2238835
PMID:37609998
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10947606/
Abstract

Arterial tonometry and vascular calcification measures are useful in cardiovascular disease (CVD) risk assessment. Prior studies found associations between tonometry measures, arterial calcium, and CVD risk. Activated platelets release angiopoietin-1 and other factors, which may connect vascular structure and platelet function. We analyzed arterial tonometry, platelet function, aortic, thoracic and coronary calcium, and thoracic and abdominal aorta diameters measured in the Framingham Heart Study Gen3/NOS/OMNI-2 cohorts ( = 3,429, 53.7% women, mean age 54.4 years ±9.3). Platelet reactivity in whole blood or platelet-rich plasma was assessed using 5 assays and 7 agonists. We analyzed linear mixed effects models with platelet reactivity phenotypes as outcomes, adjusting for CVD risk factors and family structure. Higher arterial calcium trended with higher platelet reactivity, whereas larger aortic diameters trended with lower platelet reactivity. Characteristic impedance (Zc) and central pulse pressure positively trended with various platelet traits, while pulse wave velocity and Zc negatively trended with collagen, ADP, and epinephrine traits. All results did not pass a stringent multiple test correction threshold ( < 2.22e-04). The diameter trends were consistent with lower shear environments invoking less platelet reactivity. The vessel calcium trends were consistent with subclinical atherosclerosis and platelet activation being inter-related.

摘要

动脉张力测量和血管钙化测量可用于心血管疾病 (CVD) 风险评估。先前的研究发现张力测量值、动脉钙与 CVD 风险之间存在关联。活化的血小板释放血管生成素-1 和其他因子,这些因子可能连接血管结构和血小板功能。我们分析了弗雷明汉心脏研究 Gen3/NOS/OMNI-2 队列(n=3429,53.7%为女性,平均年龄 54.4±9.3 岁)中的动脉张力测量、血小板功能、主动脉、胸和冠状动脉钙以及胸和腹主动脉直径。使用 5 种测定法和 7 种激动剂评估全血或富含血小板的血浆中的血小板反应性。我们分析了线性混合效应模型,将血小板反应性表型作为结局,调整 CVD 危险因素和家族结构。动脉钙越高,血小板反应性越高,而主动脉直径越大,血小板反应性越低。特征阻抗 (Zc) 和中心脉搏压与各种血小板特征呈正相关,而脉搏波速度和 Zc 与胶原、ADP 和肾上腺素特征呈负相关。所有结果均未通过严格的多重检验校正阈值(<2.22e-04)。直径趋势与较低的剪切环境一致,剪切环境较低会导致血小板反应性降低。血管钙趋势与亚临床动脉粥样硬化和血小板激活相互关联一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/10947606/8906a66cb7c9/nihms-1923445-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/10947606/92ece3d5e713/nihms-1923445-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/10947606/8906a66cb7c9/nihms-1923445-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/10947606/92ece3d5e713/nihms-1923445-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7948/10947606/8906a66cb7c9/nihms-1923445-f0002.jpg

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