White Blood Cell Count and Major Adverse Cardiovascular Events After Percutaneous Coronary Intervention in the Contemporary Era Insights From the PARIS Study (Patterns of Non-Adherence to Anti-Platelet Regimens in Stented Patients Registry)

被引:37
|
作者
Shah, Binita [1 ,2 ]
Baber, Usman [3 ]
Pocock, Stuart J. [4 ]
Krucoff, Mitchell W. [5 ]
Ariti, Cono [4 ]
Gibson, C. Michael [6 ]
Steg, Philippe Gabriel [7 ]
Weisz, Giora [8 ]
Witzenbichler, Bernhard [9 ]
Henry, Timothy D. [10 ,11 ]
Kini, Annapoorna S. [3 ]
Stuckey, Thomas [12 ]
Cohen, David J. [13 ]
Iakovou, Ioannis [14 ]
Dangas, George [3 ]
Aquino, Melissa B. [3 ]
Sartori, Samantha [3 ]
Chieffo, Alaide [15 ]
Moliterno, David J. [16 ]
Colombo, Antonio [15 ]
Mehran, Roxana [3 ]
机构
[1] Manhattan VA Hosp, New York Harbor Hlth Care Syst, Dept Med Cardiol, New York, NY USA
[2] NYU, Sch Med, Dept Med Cardiol, New York, NY 10003 USA
[3] Icahn Sch Med Mt Sinai, Dept Med Cardiol, New York, NY 10029 USA
[4] London Sch Hyg & Trop Med, Med Stat, London, England
[5] Duke Univ, Sch Med, Dept Med Cardiol, Durham, NC USA
[6] Harvard Med Sch, Dept Med Cardiol, Cambridge, MA USA
[7] Hop Bichat Claude Bernard, Dept Med Cardiol, Paris, France
[8] Columbia Univ, Med Ctr, Dept Med Cardiol, New York, NY USA
[9] HELIOS Amper Klinikum, Dept Med Cardiol, Dachau, Germany
[10] Cedars Sinai Heart Inst, Dept Med Cardiol, Los Angeles, CA USA
[11] Univ Minnesota, Minneapolis Heart Inst Fdn, Dept Med Cardiol, Minneapolis, MN USA
[12] LeBauer Cardiovasc Res Fdn, Moses Cone Heart & Vasc Ctr, Dept Med Cardiol, Greensboro, NC USA
[13] Univ Missouri Kansas City, St Lukes Mid Amer Heart Inst, Dept Med Cardiol, Kansas City, MO USA
[14] Onassis Cardiac Surg Ctr, Dept Med Cardiol, Athens, Greece
[15] Osped San Raffaele, Dept Med Cardiol, Milan, Italy
[16] Univ Kentucky, Dept Med Cardiol, Lexington, KY USA
关键词
acute coronary syndrome; coronary artery disease; leukocytes; myocardial infarction; percutaneous coronary intervention; PLATELET-LEUKOCYTE INTERACTIONS; ACUTE MYOCARDIAL-INFARCTION; INTEGRIN MAC-1 CD11B/CD18; RANDOMIZED-TRIAL; ADHESION MOLECULES; ENDOTHELIAL-CELLS; ARTERY-DISEASE; ANGIOPLASTY; ATORVASTATIN; ASSOCIATION;
D O I
10.1161/CIRCINTERVENTIONS.117.004981
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-Elevated white blood cell (WBC) count is associated with increased major adverse cardiovascular events (MACE) in the setting of acute coronary syndrome. The aim of this study was to evaluate whether similar associations persist in an all-comers population of patients undergoing percutaneous coronary intervention in the contemporary era. Methods and Results-In the multicenter, prospective, observational PARIS study (Patterns of Non-Adherence to Anti-Platelet Regimens in Stented Patients Registry), 4222 patients who underwent percutaneous coronary intervention in the United States and Europe between July 1, 2009, and December 2, 2010, were evaluated. The associations between baseline WBC and MACE (composite of cardiac death, stent thrombosis, spontaneous myocardial infarction, or target lesion revascularization) at 24-month follow-up were analyzed using multivariable Cox regression. Patients with higher WBC were more often younger, smokers, and with less comorbid risk factors compared with those with lower WBC. After adjustment for baseline and procedural characteristics, WBC remained independently associated with MACE (hazard ratio [HR] per 103 cells/L increase, 1.05 [95% confidence intervals (CI), 1.02-1.09]; P=0.001), cardiac death (HR, 1.10 [95% CI, 1.05-1.17]; P<0.001), and clinically indicated target revascularization (HR, 1.04 [95% CI, 1.00-1.09]; P=0.03) but not stent thrombosis (HR, 1.07 [95% CI, 0.99-1.16]; P=0.10) or spontaneous myocardial infarction (HR, 1.03 [95% CI, 0.97-1.09]; P=0.29). The association between WBC and MACE was consistent in acute coronary syndrome and non-acute coronary syndrome presentations (interaction P=0.15). Conclusions-Increased WBC is an independent predictor of MACE after percutaneous coronary intervention in a contemporary all-comers cohort. Further studies to delineate the underlying pathophysiologic role of elevated WBC across a spectrum of coronary artery disease presentations are warranted.
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