Association between cell-derived microparticles and adverse events in patients with nonpulsatile Left ventricular assist devices

被引:42
作者
Nascimbene, Angelo [1 ]
Hernandez, Ruben [2 ]
George, Joggy K. [1 ]
Parker, Anita [2 ]
Bergeron, Angela L. [3 ]
Pradhan, Subhashree [3 ]
Vijayan, K. Vinod [3 ]
Civitello, Andrew [1 ]
Simpson, Leo
Nawrot, Maria [4 ]
Lee, Vei-Vei [5 ]
Mallidi, Hari R. [2 ]
Delgado, Reynolds M. [1 ]
Dong, Jing Fei [4 ,6 ]
Frazier, O. H. [2 ]
机构
[1] Texas Heart Inst, Dept Cardiol, Houston, TX 77225 USA
[2] Texas Heart Inst, Dept Cardiovasc Surg, Houston, TX 77225 USA
[3] Baylor Coll Med, Dept Med, Div Thrombosis Res, Houston, TX 77030 USA
[4] Puget Sound Blood Ctr, Seattle, WA 98104 USA
[5] Texas Heart Inst, Div Biostat & Epidemiol, Houston, TX 77225 USA
[6] Univ Washington, Sch Med, Dept Med, Div Hematol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
ventricular assist device; cell-derived microparticles; phosphatidylserine; CORONARY-ARTERY-DISEASE; HEARTMATE II; SHEAR-STRESS; PLATELET; THROMBOGENICITY; IMPLANTATION; ACTIVATION; APOPTOSIS; STENOSIS;
D O I
10.1016/j.healun.2014.01.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: Continuous-flow left ventricular assist devices (LVADs) expose blood cells to high shear stress, potentially resulting in the production of microparticles that express phosphatidylserine (PS+) and promote coagulation and inflammation. In this prospective study, we attempted to determine whether PS+ microparticle levels correlate with clinical outcomes in LVAD-supported patients. METHODS: We enrolled 20 patients undergoing implantation of the HeartMate II LVAD (Thoratec Corp, Pleasanton, CA) and 10 healthy controls who provided reference values for the microparticle assays. Plasma was collected before LVAD implantation, at discharge, at the 3-month follow-up, and when an adverse clinical event occurred. We quantified PS+ microparticles in the plasma using flow cytometry. RESULTS: During the study period, 8 patients developed adverse clinical events: ventricular tachycardia storm in 1, non ST-elevation myocardial infarction in 2, arterial thrombosis in 2, gastrointestinal bleeding in 2, and stroke in 3. Levels of PS+ microparticles were higher in patients at baseline than in healthy controls (2.11% +/- 1.26% vs 0.69% +/- 0.46%, p = 0.007). After LVAD implantation, patient PS+ microparticle levels increased to 2.39% +/- 1.22% at discharge and then leveled to 1.97% +/- 1.25% at the 3-month follow-up. Importantly, levels of PS+ microparticles were significantly higher in patients who developed an adverse event than in patients with no events (3.82% +/- 1.17% vs 1.57% +/- 0.59%, p < 0.001), even though the 2 patient groups did not markedly differ in other clinical and hematologic parameters. CONCLUSIONS: Our results suggest that an elevation of PS+ microparticle levels may be associated, with adverse clinical events. Thus, measuring PS+ microparticle levels in LVAD-supported patients may help identify patients at increased risk for adverse events. (C) 2014 International Society for Heart and Lung Transplantation. All rights reserved,
引用
收藏
页码:470 / 477
页数:8
相关论文
共 29 条
[1]   Cellular microparticles in the pathogenesis of pulmonary hypertension [J].
Amabile, Nicolas ;
Guignabert, Christophe ;
Montani, David ;
Yeghiazarians, Yerem ;
Boulanger, Chantal M. ;
Humbert, Marc .
EUROPEAN RESPIRATORY JOURNAL, 2013, 42 (01) :272-279
[2]   Assessment of hemolysis related quantities in a microaxial blood pump by computational fluid dynamics [J].
Apel, J ;
Paul, R ;
Klaus, S ;
Siess, T ;
Reul, H .
ARTIFICIAL ORGANS, 2001, 25 (05) :341-347
[3]   Fluid mechanics of arterial stenosis: Relationship to the development of mural thrombus [J].
Bluestein, D ;
Niu, LJ ;
Schoephoerster, RT ;
Dewanjee, MK .
ANNALS OF BIOMEDICAL ENGINEERING, 1997, 25 (02) :344-356
[4]   Device thrombogenicity emulation: A novel methodology for optimizing the thromboresistance of cardiovascular devices [J].
Bluestein, Danny ;
Einav, Shmuel ;
Slepian, Marvin J. .
JOURNAL OF BIOMECHANICS, 2013, 46 (02) :338-344
[5]   Microparticles Induce Cell Cycle Arrest Through Redox-Sensitive Processes in Endothelial Cells: Implications in Vascular Senescence [J].
Burger, Dylan ;
Kwart, Dylan G. ;
Montezano, Augusto C. ;
Read, Naomi C. ;
Kennedy, Christopher R. J. ;
Thompson, Charlie S. ;
Touyz, Rhian M. .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2012, 1 (03)
[6]   Gastrointestinal bleeding rates in recipients of nonpulsatile and pulsatile left ventricular assist devices [J].
Crow, Sheri ;
John, Ranjit ;
Boyle, Andrew ;
Shumway, Sara ;
Liao, Kenneth ;
Colvin-Adams, Monica ;
Toninato, Carol ;
Missov, Emil ;
Pritzker, Marc ;
Martin, Cindy ;
Garry, Daniel ;
Thomas, William ;
Joyce, Lyle .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2009, 137 (01) :208-215
[7]   Arteriovenous malformation and gastrointestinal bleeding in patients with the HeartMate II left ventricular assist device [J].
Demirozu, Zumrut T. ;
Radovancevic, Rajko ;
Hochman, Lyone F. ;
Gregoric, Igor D. ;
Letsou, George V. ;
Kar, Biswajit ;
Bogaev, Roberta C. ;
Frazier, O. H. .
JOURNAL OF HEART AND LUNG TRANSPLANTATION, 2011, 30 (08) :849-853
[8]   Increased levels of circulating microparticles in patients with severe aortic valve stenosis [J].
Diehl, Philipp ;
Nagy, Ferenc ;
Sossong, Verena ;
Helbing, Thomas ;
Beyersdorf, Friedhelm ;
Olschewski, Manfred ;
Bode, Christoph ;
Moser, Martin .
THROMBOSIS AND HAEMOSTASIS, 2008, 99 (04) :711-719
[9]   Enhanced microparticles in ventricular assist device patients predict platelet, leukocyte and endothelial cell activation [J].
Diehl, Philipp ;
Aleker, Miriam ;
Helbing, Thomas ;
Sossong, Verena ;
Beyersdorf, Friedhelm ;
Olschewski, Manfred ;
Bode, Christoph ;
Moser, Martin .
INTERACTIVE CARDIOVASCULAR AND THORACIC SURGERY, 2010, 11 (02) :133-137
[10]   Platelet-derived exosomes induce endothelial cell apoptosis through peroxynitrite generation: experimental evidence for a novel mechanism of septic vascular dysfunction [J].
Gambim, Marcela Helena ;
Do Carmo, Alipio De Oliveira ;
Marti, Luciana ;
Verissimo-Filho, Sidney ;
Lopes, Lucia Rossetti ;
Janiszewski, Mariano .
CRITICAL CARE, 2007, 11 (05)