TY - JOUR
T1 - Statin Treatment by Low-Density Lipoprotein Cholesterol Levels in Patients With Non-ST-Segment Elevation Myocardial Infarction/Unstable Angina Pectoris (from the CRUSADE Registry)
AU - O'Brien, Emily C.
AU - Simon, Da Juanicia N.
AU - Roe, Matthew T.
AU - Wang, Tracy Y.
AU - Peterson, Eric D.
AU - Alexander, Karen P.
N1 - Funding Information:
CRUSADE was funded by Millennium Pharmaceuticals (Cambridge, MA), Schering-Plough Corporation (Kenilworth, NJ), and the Bristol-Myers Squibb/Sanofi Pharmaceuticals (New York, NY) partnership. This work was supported internally by the Duke Clinical Research Institute (Durham, NC), which donated support for these analyses. Dr. Alexander reports research funding from Gilead Pharmaceuticals (Foster City, CA), Regeneron (Tarrytown, NY), and Sanofi-Aventis (Bridgewater, NJ) (all modest) and consulting for CytRx (modest). Dr. Wang reports institutional research grant support from Eli Lilly and Company , Daiichi-Sankyo (Parsippany, NJ), Gilead Sciences (Foster City, CA), GlaxoSmithKline (Durham, NC), and the American College of Cardiology (Washington, DC) and honoraria from AstraZeneca and the American College of Cardiology. Dr. Roe reports research funding from Eli Lilly and Company (Indianapolis, IN), KAI Pharmaceuticals (South San Francisco, CA), and Sanofi-Aventis (all significant); educational activities or lectures for AstraZeneca and Janssen Pharmaceuticals (both modest); and consulting for Bristol Myers Squibb (New York, NY), Eli Lilly and Company, Glaxo Smith Kline, and Regeneron (Tarrytown, NY) (all modest) and Merck & Co. (Kenilworth, NJ), Janssen Pharmaceuticals (Raritan, NJ), and Daiichi-Sankyo (all significant). Dr. Peterson reports research funding from Eli Lilly and Company , Ortho-McNeil-Janssen Pharmaceuticals, Inc. (Raritan, NJ) , Society of Thoracic Surgeons , American Heart Association (Chicago, IL) , American College of Cardiology (Dallas, TX) (all significant) and consulting for AstraZeneca, Boehringer Ingelheim (Ridgefield, CT), Genentech (South San Francisco, CA), Johnson & Johnson (Raritan, NJ), Ortho-McNeil-Janssen Pharmaceuticals, Inc. (Raritan, NJ), Pfizer (New York, NY), Sanofi-Aventis, and WebMD (New York, NY) (all modest). Dr. O'Brien and Simon have no relevant conflicts of interest to report.
Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/6/15
Y1 - 2015/6/15
N2 - Elevated low-density lipoprotein cholesterol (LDL-C) is associated with increased risk of myocardial infarction and is a target for disease prevention. The association between initial LDL-C and statin treatment in patients with non-ST-segment elevation myocardial infarction (NSTEMI)/unstable angina pectoris (UAP) has not been well characterized. We explored detailed LDL-C levels and statin treatment in 22,938 patients with NSTEMI/UAP enrolled in the Can Rapid Risk Stratification of Unstable Angina Patients Suppress Adverse Outcomes With Early Implementation of the American College of Cardiology/American Heart Association Guidelines Registry (2003 to 2006). Patients reporting home statin use or previous cardiovascular disease were excluded. We examined statin receipt at discharge across 4 categories of baseline LDL-C: very low (<70 mg/dl), low (70 to 99 mg/dl), high (100 to 129 mg/dl), and very high (≥130 mg/dl). The largest proportion of patients had LDL-C ≥130 mg/dl (32.6%), followed by LDL-C 100 to 129 mg/dl (32.1%), LDL-C 70 to 99 mg/dl (24.9%), and LDL-C <70 mg/dl (10.4%). Compared with high LDL-C categories, patients in the lowest LDL-C category had their first NSTEMI/UAP event at a significantly older age and had higher rates of other cardiovascular risk factors (including hypertension and diabetes) but were less likely to have a family history of coronary artery disease. Overall, 80.3% of eligible patients with NSTEMI/UAP received statins at discharge, ranging from 63.8% in those with very low LDL-C (<70 mg/dl) to 88.1% in those with very high LDL-C (>130 mg/dl). In conclusion, >1/3 of patients with NSTEMI/UAP had an LDL-C level <100. Those with low LDL-C were older, had more co-morbidities, and were less likely to be prescribed a statin at discharge than those with higher LDL-C.
AB - Elevated low-density lipoprotein cholesterol (LDL-C) is associated with increased risk of myocardial infarction and is a target for disease prevention. The association between initial LDL-C and statin treatment in patients with non-ST-segment elevation myocardial infarction (NSTEMI)/unstable angina pectoris (UAP) has not been well characterized. We explored detailed LDL-C levels and statin treatment in 22,938 patients with NSTEMI/UAP enrolled in the Can Rapid Risk Stratification of Unstable Angina Patients Suppress Adverse Outcomes With Early Implementation of the American College of Cardiology/American Heart Association Guidelines Registry (2003 to 2006). Patients reporting home statin use or previous cardiovascular disease were excluded. We examined statin receipt at discharge across 4 categories of baseline LDL-C: very low (<70 mg/dl), low (70 to 99 mg/dl), high (100 to 129 mg/dl), and very high (≥130 mg/dl). The largest proportion of patients had LDL-C ≥130 mg/dl (32.6%), followed by LDL-C 100 to 129 mg/dl (32.1%), LDL-C 70 to 99 mg/dl (24.9%), and LDL-C <70 mg/dl (10.4%). Compared with high LDL-C categories, patients in the lowest LDL-C category had their first NSTEMI/UAP event at a significantly older age and had higher rates of other cardiovascular risk factors (including hypertension and diabetes) but were less likely to have a family history of coronary artery disease. Overall, 80.3% of eligible patients with NSTEMI/UAP received statins at discharge, ranging from 63.8% in those with very low LDL-C (<70 mg/dl) to 88.1% in those with very high LDL-C (>130 mg/dl). In conclusion, >1/3 of patients with NSTEMI/UAP had an LDL-C level <100. Those with low LDL-C were older, had more co-morbidities, and were less likely to be prescribed a statin at discharge than those with higher LDL-C.
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U2 - 10.1016/j.amjcard.2015.03.007
DO - 10.1016/j.amjcard.2015.03.007
M3 - Article
C2 - 25888303
AN - SCOPUS:84930180844
SN - 0002-9149
VL - 115
SP - 1655
EP - 1660
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 12
M1 - 21045
ER -