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 inJournal of thrombosis and thrombolysis Vol. 27; no. 1; pp. 24 - 28
Main Authors Tirnaksiz, Ebru, Pamukcu, Burak, Oflaz, Huseyin, Nisanci, Yilmaz
Format Journal Article
LanguageEnglish
Published Boston Springer US 01.01.2009
Springer Nature B.V
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Online AccessGet full text
ISSN0929-5305
1573-742X
DOI10.1007/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.
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
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  fullname: Tirnaksiz, Ebru
  organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University
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  givenname: Burak
  surname: Pamukcu
  fullname: Pamukcu, Burak
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  organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University
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  fullname: Oflaz, Huseyin
  organization: Department of Cardiology, Istanbul Faculty of Medicine, Istanbul University
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  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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PublicationSubtitle A Journal for Translation, Application and Therapeutics
PublicationTitle Journal of thrombosis and thrombolysis
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1991840 - J Clin Invest. 1991 Feb;87(2):571-80
12827283 - Cell Mol Life Sci. 2003 May;60(5):961-71
15990752 - Am Heart J. 2005 Apr;149(4):675-80
7660152 - Semin Thromb Hemost. 1995;21 Suppl 2:113-21
10700490 - Stroke. 2000 Mar;31(3):591-5
12114036 - Lancet. 2002 Jul 6;360(9326):7-22
15757620 - Am J Cardiol. 2005 Mar 15;95(6):805-8
10636252 - J Am Coll Cardiol. 2000 Jan;35(1):1-10
10952950 - Circulation. 2000 Aug 22;102(8):840-5
9241100 - Br J Clin Pharmacol. 1997 Jul;44(1):77-83
16133890 - J Thromb Thrombolysis. 2005 Aug;20(1):17-22
8181117 - Circulation. 1994 May;89(5):1951-7
12534449 - Eur J Clin Invest. 2002 Dec;32(12):901-8
11888512 - Atherosclerosis. 2002 Apr;161(2):301-6
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3884719 - J Lab Clin Med. 1985 Apr;105(4):479-83
14871160 - CNS Drugs. 2004;18(3):165-72
11514380 - Circulation. 2001 Aug 21;104(8):921-7
15255464 - Acta Cardiol. 2004 Jun;59(3):311-5
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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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https://www.ncbi.nlm.nih.gov/pubmed/17917708
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