TY - JOUR
T1 - LDL-C Targets in Secondary Prevention
T2 - How Low Should We Go?
AU - Bayoumy, Karim
AU - Gaber, Mohammed
AU - Mani, Preethi
AU - Puri, Rishi
AU - Donnellan, Eoin
AU - Cho, Leslie
AU - Clark, Donald
AU - Martin, Seth S.
AU - Elshazly, Mohamed B.
N1 - Funding Information:
Conflict of Interest DCIII reports has received grant support from the American Heart Association. SSM has served on scientific advisory boards of Amgen, Sanofi, Regeneron, Esperion, Novo Nordisk, Quest Diagnostics, and Akcea Therapeutics, and has received research support from Apple, Google, iHealth, Nokia, NIH, the Maryland Innovation Initiative, American Heart Association, Aetna Foundation, PJ Schafer Memorial Fund, and David and June Trone Family Foundation. He is a co-inventor on a pending patent filed by Johns Hopkins University for a system of LDL-C estimation. All other authors report no relevant financial disclosures.
Publisher Copyright:
© 2019, The Author(s).
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Purpose of Review: The benefits of lowering low-density lipoprotein cholesterol (LDL-C), mainly using high-intensity statin therapy, and its impact on decreasing the recurrence of atherosclerotic cardiovascular disease (ASCVD) in secondary prevention has been well established. With the advent of non-statin medications, particularly PCSK-9 inhibitors, which can lower LDL-C to very low levels not seen before, it is important to answer some important questions regarding LDL-C lowering and the uses of these medications in clinical practice: how low should we go with LDL-C reduction? Is there a threshold beyond which lower LDL-C is not associated with any benefit and possibly harm? Does the benefit derived from more aggressive LDL-C lowering justify the cost of additional therapies? Recent Findings: Our review has found overwhelming evidence to support the conclusion that lower achieved LDL-C levels correlate with a decreased burden of atherosclerosis and better clinical outcomes in secondary prevention. The concern for adverse effects with very low LDL-C levels is not backed by the literature, and side effects appear to be medication-specific. There still remains a question of the cost-effectiveness of some non-statin therapies particularly PCSK9 inhibitors, in spite of recent price decreases, and whether the benefit is worth the cost. Summary: It is prudent to always pursue an individualized patient-level approach to LDL-C lowering that considers the patient’s global cardiovascular risk, their side effect profile, and the cost-effectiveness of therapies in order to derive maximal benefit from aggressive lipid lowering.
AB - Purpose of Review: The benefits of lowering low-density lipoprotein cholesterol (LDL-C), mainly using high-intensity statin therapy, and its impact on decreasing the recurrence of atherosclerotic cardiovascular disease (ASCVD) in secondary prevention has been well established. With the advent of non-statin medications, particularly PCSK-9 inhibitors, which can lower LDL-C to very low levels not seen before, it is important to answer some important questions regarding LDL-C lowering and the uses of these medications in clinical practice: how low should we go with LDL-C reduction? Is there a threshold beyond which lower LDL-C is not associated with any benefit and possibly harm? Does the benefit derived from more aggressive LDL-C lowering justify the cost of additional therapies? Recent Findings: Our review has found overwhelming evidence to support the conclusion that lower achieved LDL-C levels correlate with a decreased burden of atherosclerosis and better clinical outcomes in secondary prevention. The concern for adverse effects with very low LDL-C levels is not backed by the literature, and side effects appear to be medication-specific. There still remains a question of the cost-effectiveness of some non-statin therapies particularly PCSK9 inhibitors, in spite of recent price decreases, and whether the benefit is worth the cost. Summary: It is prudent to always pursue an individualized patient-level approach to LDL-C lowering that considers the patient’s global cardiovascular risk, their side effect profile, and the cost-effectiveness of therapies in order to derive maximal benefit from aggressive lipid lowering.
KW - Adverse effects
KW - Clinical guidelines
KW - LDL lowering
KW - PCSK9 inhibitors
KW - Secondary prevention
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U2 - 10.1007/s12170-019-0619-8
DO - 10.1007/s12170-019-0619-8
M3 - Review article
AN - SCOPUS:85067518877
SN - 1932-9520
VL - 13
JO - Current Cardiovascular Risk Reports
JF - Current Cardiovascular Risk Reports
IS - 8
M1 - 23
ER -