冠脉钙化评分与阻塞性慢性阻塞性肺病加重风险的关系

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
R Chad Wade, Sharon X Ling, Erika S Helgeson, Helen Voelker, Wassim W Labaki, Daniel Meza, Oisin O'Corragain, Jennifer Y So, Gerard J Criner, MeiLan K Han, Ravi Kalhan, Robert M Reed, Mark T Dransfield, J Michael Wells
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引用次数: 0

摘要

2019年,BLOCK-COPD(预防慢性阻塞性肺疾病急性加重的β受体阻滞剂)在无β受体阻滞剂适应症的COPD人群中评估了美托洛尔对加重风险和死亡率的影响。我们假设冠状动脉疾病(CAD)的成像指标,冠状动脉钙(CAC)评分,可以预测恶化风险,并确定对美托洛尔治疗的差异反应。方法:研究人群包括来自多个研究地点的BLOCK-COPD患者。参与者在入组后±12个月进行了临床指示的胸部CT扫描。Weston评分系统量化了CAC。校正Cox比例风险模型评估CAC与恶化时间之间的关系。结果:数据包括109名参与者。平均CAC评分为5.1±3.7,92例(84%)患者的CAC评分大于0。中位(IQR)随访时间为350(280至352)天,有61例轻度加重,19例重度/极重度加重。没有发现任何严重程度的恶化与CAC>或总CAC之间的关联。观察到总CAC和CAC>在LCx和任何严重程度恶化时间之间的相关性(aHR=1.39, CI: 1.08-1.79, p=0.01)和(aHR=1.96, 95% CI: 1.04-3.70, p= 0.04)。结论:CAD是COPD的常见合并症,可导致显著的死亡率。我们的研究使用CAC评分证实了CAD的高患病率;然而,我们没有发现CAC与恶化风险之间的关联。我们确实发现了LCX中CAC与恶化风险之间的新关联,这需要在更大的队列中进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Associations Between Coronary Artery Calcium Score and Exacerbation Risk in BLOCK-COPD.

Introduction: In 2019, the Beta-Blockers for the Prevention of Acute Exacerbations of Chronic Obstructive Pulmonary Disease study (BLOCK-COPD) evaluated the effect of metoprolol on exacerbation risk and mortality in a COPD population without indications for beta-blocker use. We hypothesized that an imaging metric of coronary artery disease (CAD), the coronary artery calcium (CAC) score, would predict exacerbation risk and identify a differential response to metoprolol treatment.

Methods: The study population includes participants in the BLOCK-COPD study from multiple study sites. Participants underwent clinically indicated thoracic computed tomography (CT) scans ± 12 months from enrollment. The Weston scoring system quantified CAC. Adjusted Cox proportional hazards models evaluated for associations between CAC and time to exacerbation.

Results: Data is included for 109 participants. The mean CAC score was 5.1±3.7, and 92 participants (84%) had CAC scores greater than 0. Over a median (interquartile range) follow-up time of 350 (280 to 352) days, there were 61 mild exacerbations and 19 severe/very severe exacerbations. No associations were found between exacerbations of any severity and CAC>0 or total CAC. Associations were observed between total CAC and CAC>0 in the left circumflex (LCx) and time to exacerbation of any severity (adjusted hazard ratio [aHR]=1.39, confidence interval [CI]: 1.08-1.79, p=0.01) and (aHR=1.96, 95% CI: 1.04-3.70, p=0.04), respectively.

Conclusions: CAD is a prevalent comorbidity in COPD accounting for significant mortality. Our study confirms the high prevalence of CAD using the CAC score; however, we did not discover an association between CAC and exacerbation risk. We did find novel associations between CAC in the LCx and exacerbation risk which warrant further investigation in larger cohorts.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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