Effect of high dose statin therapy on platelet function; statins reduce aspirin resistant platelet aggregation in patients with coronary heart disease
Background Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease. Aim Our aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease. Material and methods A total of 178...
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Published in | Journal of thrombosis and thrombolysis Vol. 27; no. 1; pp. 24 - 28 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Boston
Springer US
01.01.2009
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
ISSN | 0929-5305 1573-742X |
DOI | 10.1007/s11239-007-0154-1 |
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Abstract | Background
Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease.
Aim
Our aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease.
Material and methods
A total of 178 consecutive patients (37–68 years old, 35.9% women) with stable coronary artery disease (CAD) was enrolled in the study. Platelet function assays were realized by the Platelet Function Analyzer (PFA)-100 with collagen and epinephrine (Col/Epi) and collagen and ADP (Col/ADP) cartridges. Aspirin resistance was defined as having a closure time (CT) of <186 s with Col/Epi cartridges despite regular aspirin therapy. A statin therapy protocol applied to the patients with aspirin resistance for 3 months.
Results
We determined that 20 (11.2%) of patients had aspirin resistance by the PFA-100. Mean closure time measured with the Col/ADP cartridges was 83 ± 18 s (53–162 s). Of the patients 12 were not on a statin therapy and eight were taking 10 mg daily atorvastatin. After 3 months of 40 mg daily atorvastatin therapy 13 subjects with aspirin resistance became aspirin sensitive by PFA-100 (
P
< 0.0001). There was also a significant decrease in total and LDL cholesterol levels and an increase in HDL cholesterol at the third month of statin therapy (
P
< 0.0001 for all).
Conclusion
Statin therapy reduced the in vitro aspirin resistance in 65% of the patients after a therapy of 3 months. Further studies are needed to elucidate the mechanism of statins’ effects on platelet reactivity. |
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AbstractList | Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease.BACKGROUNDCurrent evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease.Our aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease.AIMOur aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease.A total of 178 consecutive patients (37-68 years old, 35.9% women) with stable coronary artery disease (CAD) was enrolled in the study. Platelet function assays were realized by the Platelet Function Analyzer (PFA)-100 with collagen and epinephrine (Col/Epi) and collagen and ADP (Col/ADP) cartridges. Aspirin resistance was defined as having a closure time (CT) of <186 s with Col/Epi cartridges despite regular aspirin therapy. A statin therapy protocol applied to the patients with aspirin resistance for 3 months.MATERIAL AND METHODSA total of 178 consecutive patients (37-68 years old, 35.9% women) with stable coronary artery disease (CAD) was enrolled in the study. Platelet function assays were realized by the Platelet Function Analyzer (PFA)-100 with collagen and epinephrine (Col/Epi) and collagen and ADP (Col/ADP) cartridges. Aspirin resistance was defined as having a closure time (CT) of <186 s with Col/Epi cartridges despite regular aspirin therapy. A statin therapy protocol applied to the patients with aspirin resistance for 3 months.We determined that 20 (11.2%) of patients had aspirin resistance by the PFA-100. Mean closure time measured with the Col/ADP cartridges was 83 +/- 18 s (53-162 s). Of the patients 12 were not on a statin therapy and eight were taking 10 mg daily atorvastatin. After 3 months of 40 mg daily atorvastatin therapy 13 subjects with aspirin resistance became aspirin sensitive by PFA-100 (P < 0.0001). There was also a significant decrease in total and LDL cholesterol levels and an increase in HDL cholesterol at the third month of statin therapy (P < 0.0001 for all).RESULTSWe determined that 20 (11.2%) of patients had aspirin resistance by the PFA-100. Mean closure time measured with the Col/ADP cartridges was 83 +/- 18 s (53-162 s). Of the patients 12 were not on a statin therapy and eight were taking 10 mg daily atorvastatin. After 3 months of 40 mg daily atorvastatin therapy 13 subjects with aspirin resistance became aspirin sensitive by PFA-100 (P < 0.0001). There was also a significant decrease in total and LDL cholesterol levels and an increase in HDL cholesterol at the third month of statin therapy (P < 0.0001 for all).Statin therapy reduced the in vitro aspirin resistance in 65% of the patients after a therapy of 3 months. Further studies are needed to elucidate the mechanism of statins' effects on platelet reactivity.CONCLUSIONStatin therapy reduced the in vitro aspirin resistance in 65% of the patients after a therapy of 3 months. Further studies are needed to elucidate the mechanism of statins' effects on platelet reactivity. Background Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease. Aim Our aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease. Material and methods A total of 178 consecutive patients (37–68 years old, 35.9% women) with stable coronary artery disease (CAD) was enrolled in the study. Platelet function assays were realized by the Platelet Function Analyzer (PFA)-100 with collagen and epinephrine (Col/Epi) and collagen and ADP (Col/ADP) cartridges. Aspirin resistance was defined as having a closure time (CT) of <186 s with Col/Epi cartridges despite regular aspirin therapy. A statin therapy protocol applied to the patients with aspirin resistance for 3 months. Results We determined that 20 (11.2%) of patients had aspirin resistance by the PFA-100. Mean closure time measured with the Col/ADP cartridges was 83 ± 18 s (53–162 s). Of the patients 12 were not on a statin therapy and eight were taking 10 mg daily atorvastatin. After 3 months of 40 mg daily atorvastatin therapy 13 subjects with aspirin resistance became aspirin sensitive by PFA-100 ( P < 0.0001). There was also a significant decrease in total and LDL cholesterol levels and an increase in HDL cholesterol at the third month of statin therapy ( P < 0.0001 for all). Conclusion Statin therapy reduced the in vitro aspirin resistance in 65% of the patients after a therapy of 3 months. Further studies are needed to elucidate the mechanism of statins’ effects on platelet reactivity. Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease. Our aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease. A total of 178 consecutive patients (37-68 years old, 35.9% women) with stable coronary artery disease (CAD) was enrolled in the study. Platelet function assays were realized by the Platelet Function Analyzer (PFA)-100 with collagen and epinephrine (Col/Epi) and collagen and ADP (Col/ADP) cartridges. Aspirin resistance was defined as having a closure time (CT) of <186 s with Col/Epi cartridges despite regular aspirin therapy. A statin therapy protocol applied to the patients with aspirin resistance for 3 months. We determined that 20 (11.2%) of patients had aspirin resistance by the PFA-100. Mean closure time measured with the Col/ADP cartridges was 83 +/- 18 s (53-162 s). Of the patients 12 were not on a statin therapy and eight were taking 10 mg daily atorvastatin. After 3 months of 40 mg daily atorvastatin therapy 13 subjects with aspirin resistance became aspirin sensitive by PFA-100 (P < 0.0001). There was also a significant decrease in total and LDL cholesterol levels and an increase in HDL cholesterol at the third month of statin therapy (P < 0.0001 for all). Statin therapy reduced the in vitro aspirin resistance in 65% of the patients after a therapy of 3 months. Further studies are needed to elucidate the mechanism of statins' effects on platelet reactivity. Background Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease. Aim Our aim was to determine the effects of aggressive statin therapy on platelet function in patients with coronary heart disease. Material and methods A total of 178 consecutive patients (37-68 years old, 35.9% women) with stable coronary artery disease (CAD) was enrolled in the study. Platelet function assays were realized by the Platelet Function Analyzer (PFA)-100 with collagen and epinephrine (Col/Epi) and collagen and ADP (Col/ADP) cartridges. Aspirin resistance was defined as having a closure time (CT) of <186 s with Col/Epi cartridges despite regular aspirin therapy. A statin therapy protocol applied to the patients with aspirin resistance for 3 months. Results We determined that 20 (11.2%) of patients had aspirin resistance by the PFA-100. Mean closure time measured with the Col/ADP cartridges was 83 ± 18 s (53-162 s). Of the patients 12 were not on a statin therapy and eight were taking 10 mg daily atorvastatin. After 3 months of 40 mg daily atorvastatin therapy 13 subjects with aspirin resistance became aspirin sensitive by PFA-100 (P < 0.0001). There was also a significant decrease in total and LDL cholesterol levels and an increase in HDL cholesterol at the third month of statin therapy (P < 0.0001 for all). Conclusion Statin therapy reduced the in vitro aspirin resistance in 65% of the patients after a therapy of 3 months. Further studies are needed to elucidate the mechanism of statins' effects on platelet reactivity. |
Author | Tirnaksiz, Ebru Nisanci, Yilmaz Oflaz, Huseyin Pamukcu, Burak |
Author_xml | – sequence: 1 givenname: Ebru surname: Tirnaksiz fullname: Tirnaksiz, Ebru organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University – sequence: 2 givenname: Burak surname: Pamukcu fullname: Pamukcu, Burak email: bpamukcu@gmail.com, bpamukcu@istanbul.edu.tr, bpamukcu2002@yahoo.com organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University – sequence: 3 givenname: Huseyin surname: Oflaz fullname: Oflaz, Huseyin organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University – sequence: 4 givenname: Yilmaz surname: Nisanci fullname: Nisanci, Yilmaz organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/17917708$$D View this record in MEDLINE/PubMed |
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Keywords | Arterial thrombosis PFA-100 Platelet function assays Atorvastatin Platelet hyperreactivity, Aspirin resistance Coronary heart disease Statins |
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Snippet | Background
Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease.
Aim
Our aim was to... Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease. Our aim was to determine the effects... Background Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease. Aim Our aim was to... Current evidence supports the preventive role of statins on platelet aggregation in patients with coronary heart disease.BACKGROUNDCurrent evidence supports... |
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SubjectTerms | Adenosine Diphosphate - pharmacology Adult Aged Aspirin - pharmacology Atorvastatin Calcium Cardiology Cholesterol, HDL - blood Cholesterol, LDL - blood Collagen - pharmacology Coronary Disease - blood Coronary Disease - complications Coronary Disease - drug therapy Diabetes Complications - blood Drug Resistance Epinephrine - pharmacology Female Hematology Heptanoic Acids - pharmacology Heptanoic Acids - therapeutic use Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Hypercholesterolemia - blood Hypercholesterolemia - complications Hypercholesterolemia - drug therapy Hypertension - blood Hypertension - complications Male Medicine Medicine & Public Health Middle Aged Platelet Aggregation - drug effects Platelet Function Tests Pyrroles - pharmacology Pyrroles - therapeutic use Smoking |
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Title | Effect of high dose statin therapy on platelet function; statins reduce aspirin resistant platelet aggregation in patients with coronary heart disease |
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