CBS 2019
CBSMD教育中心
English

科学研究

科研文章

荐读文献

Myocardial infarction with non-obstructive coronary arteries as compared with myocardial infarction and obstructive coronary disease: outcomes in a Medicare population Patterns of use of angiotensin-converting enzyme inhibitors/angiotensin receptor blockers among patients with acute myocardial infarction in China from 2001 to 2011: China PEACE-Retrospective AMI Study Cardiac Sympathetic Denervation for Refractory Ventricular Arrhythmias Randomized trial of complete versus lesion-only revascularization in patients undergoing primary percutaneous coronary intervention for STEMI and multivessel disease: the CvLPRIT trial Coronary Artery Plaque Characteristics Associated With Adverse Outcomes in the SCOT-HEART Study BMI, Infarct Size, and Clinical Outcomes Following Primary PCI Patient-Level Analysis From 6 Randomized Trials Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection Evidence-based detection of pulmonary arterial hypertension in systemic sclerosis: the DETECT study Long-Term Incremental Prognostic Value of Cardiovascular Magnetic Resonance After ST-Segment Elevation Myocardial Infarction A Study of the Collaborative Registry on CMR in STEMI Treatment effects of systematic two-stent and provisional stenting techniques in patients with complex coronary bifurcation lesions: rationale and design of a prospective, randomised and multicentre DEFINITION II trial

Expert Opinion2018 Apr 24;137(17):1763-1766

JOURNAL:Circulation. Article Link

Mortality Differences Associated With Treatment Responses in CANTOS and FOURIER: Insights and Implications

Ridker PM Keywords: atherosclerosis; canakinumab; evolocumab; mortality; prevention and control; randomized controlled trials as topic

ABSTRACT


Similarities and differences in 2 contemporary postrandomization on-treatment analyses from the FOURIER trial (Further Cardiovascular Outcomes Research With PCSK9 Inhibition in Subjects With Elevated Risk) and CANTOS trial (Canakinumab Antiinflammatory Thrombosis Outcome Study) may provide insight into what factors drive reductions in cardiovascular mortality and all-cause mortality among patients with atherosclerosis already treated with high-intensity statins.

In the first article, the FOURIER Investigators elegantly demonstrate that lower is better for low-density lipoprotein cholesterol (LDLC) after adjunctive therapy with the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor evolocumab. For the FOURIER primary end point (a composite of myocardial infarction, stroke, coronary revascularization, unstable angina, or cardiovascular death), there was a highly significant monotonic relationship between sequentially lower achieved LDLC concentrations and lower cardiovascular risk, extending even to those with on-treatment LDLC <20 mg/dL. This benefit was driven largely by statistically significant reductions in the trial composite end point among those with LDLC levels below the approximate on-treatment median of 50 mg/dL (for which hazard ratios ranged between 0.76 and 0.85). In contrast, marginal and nonsignificant reductions were observed among those in FOURIER with on-treatment LDLC levels >50 mg/dL (for which hazard ratios ranged from 0.94–0.97). These PCSK9 data are important because evolocumab has powerful effects on LDLC but no effect on high-sensitivity C-reactive protein (hs-CRP).

In the second article, the CANTOS Investigators similarly demonstrate that lower is better for inflammation reduction, at least with the interleukin-1β inhibitor canakinumab.2 For the CANTOS primary end point (a composite of myocardial infarction, stroke, or cardiovascular death), there was a highly significant 25% reduction among those with on-treatment hs-CRP levels below the approximate on-treatment median of 2 mg/L. In contrast, marginal and nonsignificant reductions …