首页> 外文期刊>Journal of Clinical Medicine >Pregnancy Associated Plasma Protein-A as a Cardiovascular Risk Marker in Patients with Stable Coronary Heart Disease During 10 Years Follow-Up—A CLARICOR Trial Sub-Study
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Pregnancy Associated Plasma Protein-A as a Cardiovascular Risk Marker in Patients with Stable Coronary Heart Disease During 10 Years Follow-Up—A CLARICOR Trial Sub-Study

机译:怀孕相关的血浆蛋白-A作为患有冠心病患者的心血管风险标志,在10年后的后续后续康复者试验子研究

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Elevated pregnancy-associated plasma protein A (PAPP-A) is associated with mortality in acute coronary syndromes. Few studies have assessed PAPP-A in stable coronary artery disease (CAD) and results are conflicting. We assessed the 10-year prognostic relevance of PAPP-A levels in stable CAD. The CLARICOR trial was a randomized controlled clinical trial including outpatients with stable CAD, randomized to clarithromycin versus placebo. The placebo group constituted our discovery cohort ( n = 1.996) and the clarithromycin group the replication cohort ( n = 1.975). The composite primary outcome was first occurrence of cardiovascular event or death. In the discovery cohort, incidence rates (IR) for the composite outcome were higher in those with elevated PAPP-A (IR 12.72, 95% Confidence Interval (CI) 11.0–14.7 events/100 years) compared to lower PAPP-A (IR 8.78, 8.25–9.34), with comparable results in the replication cohort. Elevated PAPP-A was associated with increased risk of the composite outcome in both cohorts (discovery Hazard Ratio (HR) 1.45, 95% CI 1.24–1.70; replication HR 1.29, 95% CI 1.10–1.52). In models adjusted for established risk factors, these trends were attenuated. Elevated PAPP-A was associated with higher all-cause mortality in both cohorts. We conclude that elevated PAPP-A levels are associated with increased long-term mortality in stable CAD, but do not improve long-term prediction of death or cardiovascular events when added to established predictors.
机译:妊娠相关的血浆蛋白A(PAPP-A)升高与急性冠状动脉综合征中的死亡率有关。很少有研究评估稳定的冠状动脉疾病(CAD)中的PAPP-A,结果是矛盾的。我们评估了稳定CAD中PAPP-A水平的10年性预后相关性。克朗者试验是随机对照临床试验,包括具有稳定CAD的门诊,随机向克拉霉素与安慰剂。安慰剂组构成了我们的发现队列(n = 1.996)和克拉霉素组复制队列(n = 1.975)。复合主要结果是第一次发生心血管事件或死亡。在与较低PAPP-A(IR 8.78,8.25-9.34),具有可比结果的复制队列。升高的PAPP-A与群组中复合结果的风险增加(发现危害比(HR)1.45,95%CI 1.24-1.70;复制HR 1.29,95%CI 1.10-1.52)。在适用于既定风险因素的模型中,这些趋势已衰减。升高的PAPP-A与两个队列中的较高的全导致死亡率相关联。我们得出结论,升高的PAPP-A水平与稳定的CAD中的长期死亡率提高,但在添加到建立的预测因子时,不会改善死亡或心血管事件的长期预测。

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