Effects of different doses, enteric-coated preparation of aspirin, and sex on urinary 11-dehydrothromboxane B2 in healthy volunteers

被引:6
作者
Dharmasaroja, Pornpatr A. [1 ]
Sae-Lim, Suvaraporn [2 ]
机构
[1] Thammasat Univ, Fac Med, Div Neurol, Dept Internal Med, Klongluang 12120, Pathumthani, Thailand
[2] Thammasat Univ, Fac Med, Res Unit, Klongluang 12120, Pathumthani, Thailand
关键词
antiplatelet; aspirin; urine dehydrothromboxane; CORONARY-ARTERY-DISEASE; PLATELET-FUNCTION TESTS; CARDIOVASCULAR EVENTS; RESISTANCE; STROKE; RISK; RESPONSIVENESS; METAANALYSIS;
D O I
10.1097/MBC.0b013e32833cea2c
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There is scarce information about the effects of different doses and enteric-coated preparation of aspirin on platelet function, especially in Asian people, evaluated by the measurement of urinary 11-dehydrothromboxane B2 (dTXB2). The objective of the present study was to assess the effects of different doses, enteric-coated preparation of aspirin, sex and also the effects of timing of urine collection on urinary dTXB2 level in healthy volunteers. Thirty healthy volunteers were included. Each volunteer took three preparations of aspirin (aspirin 81 mg, enteric-coated aspirin 300mg and aspirin 300 mg) for 7 days. Urine dTXB2 level was measured at baseline, day 3, and day 7 after taking each preparation of aspirin. There was no significant difference in the effects of different doses of aspirin (81 vs. 300 mg, 50.7 vs. 61.8 ng/mmol creatinine, P=0.248), preparations (enteric-coated vs. nonenteric-coated aspirin, 61.8 vs. 67.9 ng/mmol creatinine, P=0.527) and time of urine collection (day 3 vs. day 7, 51.7 vs. 49.9 ng/mmol creatinine, P=0.448). Female volunteers showed a trend to have higher urinary dTXB2 than male volunteers at baseline and after taking aspirin. This study showed no significant difference in urinary dTXB2 level after taking different doses and enteric-coated preparation of aspirin in healthy volunteers. Blood Coagul Fibrinolysis 21:649-652 (c) 2010 Wolters Kluwer Health | Lippincott Williams & Wilkins.
引用
收藏
页码:649 / 652
页数:4
相关论文
共 20 条
[1]   Antiplatelet effect of aspirin in patients with cerebrovascular disease [J].
Alberts, MJ ;
Bergman, DL ;
Molner, E ;
Jovanovic, BD ;
Ushiwata, I ;
Teruya, J .
STROKE, 2004, 35 (01) :175-178
[2]   Aspirin non-responsiveness as measured by PFA-100 in patients with coronary artery disease [J].
Andersen, K ;
Hurlen, M ;
Arnesen, H ;
Seljeflot, I .
THROMBOSIS RESEARCH, 2002, 108 (01) :37-42
[3]   Aspirin and urinary 11-dehydrothromboxane B2 in African American stroke patients [J].
Bruno, A ;
McConnell, JP ;
Mansbach, HH ;
Cohen, SN ;
Tietjen, GE ;
Bang, NU .
STROKE, 2002, 33 (01) :57-60
[4]   Aspirin-resistant thromboxane biosynthesis and the risk of myocardial infarction, stroke, or cardiovascular death in patients at high risk for cardiovascular events [J].
Eikelboom, JW ;
Hirsh, J ;
Weitz, JI ;
Johnston, M ;
Yi, Q ;
Yusuf, S .
CIRCULATION, 2002, 105 (14) :1650-1655
[5]  
Fritsma G A, 2001, JAAPA, V14, P57
[6]   Evaluation of dose-related effects of aspirin on platelet function - Results from the aspirin-induced platelet effect (ASPECT) study [J].
Gurbel, Paul A. ;
Bliden, Kevin P. ;
DiChiara, Joseph ;
Newcomer, Justin ;
Weng, Willy ;
Neerchal, Nagaraj K. ;
Gesheff, Tania ;
Chaganti, Srivasavi K. ;
Etherington, Amena ;
Tantry, Udaya S. .
CIRCULATION, 2007, 115 (25) :3156-3164
[7]   Aspirin resistance - May be a cause of recurrent ischaemic vascular events in patients taking aspirin [J].
Hankey, GJ ;
Eikelboom, JW .
BMJ-BRITISH MEDICAL JOURNAL, 2004, 328 (7438) :477-479
[8]   Lack of reproducibility of assessment of aspirin responsiveness by optical aggregometry and two platelet function tests [J].
Harrison, Paul ;
Segal, Helen ;
Silver, Louise ;
Syed, Anila ;
Cuthbertson, Fiona C. ;
Rothwell, Peter M. .
PLATELETS, 2008, 19 (02) :119-124
[9]  
HECKEN AV, 2002, ALIMENT PHARM THER, V16, P1683
[10]   Aspirin responsiveness in healthy volunteers measured with multiple assay platforms [J].
Karon, Brad S. ;
Wockenfus, Amy ;
Scott, Renee ;
Hartman, Stacy J. ;
McConnell, Joseph P. ;
Santrach, Paula J. ;
Jaffe, Allan S. .
CLINICAL CHEMISTRY, 2008, 54 (06) :1060-1065