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特定年龄和性别的基因表达评分与血运重建及冠状动脉疾病相关:胸痛评估前瞻性多中心成像研究(PROMISE)试验的见解

An age- and sex-specific gene expression score is associated with revascularization and coronary artery disease: Insights from the Prospective Multicenter Imaging Study for Evaluation of Chest Pain (PROMISE) trial.

作者信息

Voora Deepak, Coles Adrian, Lee Kerry L, Hoffmann Udo, Wingrove James A, Rhees Brian, Huang Lin, Daniels Susan E, Monane Mark, Rosenberg Steven, Shah Svati H, Kraus William E, Ginsburg Geoffrey S, Douglas Pamela S

机构信息

Duke Center for Applied Genomics & Precision Medicine, Duke University School of Medicine, Durham, NC; Department of Medicine, Duke University School of Medicine, Durham, NC.

Duke Clinical Research Institute, Duke University School of Medicine, Durham, NC.

出版信息

Am Heart J. 2017 Feb;184:133-140. doi: 10.1016/j.ahj.2016.11.004. Epub 2016 Nov 15.

Abstract

BACKGROUND

Identifying predictors of coronary artery disease (CAD)-related procedures and events remains a priority.

METHODS

We measured an age- and sex-specific gene expression score (ASGES) previously validated to detect obstructive CAD (oCAD) in symptomatic nondiabetic patients in the PROMISE trial. The outcomes were oCAD (≥70% stenosis in ≥1 vessel or ≥50% left main stenosis on CT angiography [CTA]) and a composite endpoint of death, myocardial infarction, revascularization, or unstable angina.

RESULTS

The ASGES was determined in 2370 nondiabetic participants (47.5% male, median age 59.5 years, median follow-up 25 months), including 1137 with CTA data. An ASGES >15 was associated with oCAD (odds ratio 2.5 [95% CI 1.6-3.8], P<.001) and the composite endpoint (hazard ratio [HR] 2.6 [95% CI 1.8-3.9], P<.001) in unadjusted analyses. After adjustment for Framingham risk, an ASGES >15 remained associated with the composite endpoint (P=.02); the only component that was associated was revascularization (adjusted HR 2.69 [95% CI 1.52-4.79], P<.001). Compared to noninvasive testing, the ASGES improved prediction for the composite (increase in c-statistic=0.036; continuous net reclassification index=43.2%). Patients with an ASGES ≤15 had a composite endpoint rate no different from those with negative noninvasive test results (3.2% vs. 2.6%, P=.29).

CONCLUSIONS

A blood-based genomic test for detecting oCAD significantly predicts near-term revascularization procedures, but not non-revascularization events. Larger studies will be needed to clarify the risk with non-revascularization events.

摘要

背景

确定冠状动脉疾病(CAD)相关手术和事件的预测因素仍然是一个优先事项。

方法

我们测量了先前在PROMISE试验中经过验证可用于检测有症状非糖尿病患者阻塞性CAD(oCAD)的年龄和性别特异性基因表达评分(ASGES)。结局指标为oCAD(CT血管造影[CTA]显示≥1支血管狭窄≥70%或左主干狭窄≥50%)以及死亡、心肌梗死、血运重建或不稳定型心绞痛的复合终点。

结果

在2370名非糖尿病参与者(男性占47.5%,中位年龄59.5岁,中位随访25个月)中确定了ASGES,其中1137人有CTA数据。在未校正分析中,ASGES>15与oCAD(比值比2.5[95%CI 1.6 - 3.8],P<.001)和复合终点(风险比[HR]2.6[95%CI 1.8 - 3.9],P<.001)相关。在对弗雷明汉风险进行校正后,ASGES>15仍与复合终点相关(P = .02);唯一相关的组成部分是血运重建(校正后HR 2.69[95%CI 1.52 - 4.79],P<.001)。与非侵入性检测相比,ASGES改善了对复合终点的预测(c统计量增加 = 0.036;连续净重新分类指数 = 43.2%)。ASGES≤15的患者复合终点发生率与非侵入性检测结果为阴性的患者无差异(3.2%对2.6%,P = .29)。

结论

一种用于检测oCAD的基于血液的基因组检测可显著预测近期血运重建手术,但不能预测非血运重建事件。需要更大规模的研究来阐明非血运重建事件的风险。

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