TY - JOUR
T1 - The Residual Risk Reduction Initiative
T2 - A Call to Action to Reduce Residual Vascular Risk in Patients with Dyslipidemia
AU - Fruchart, Jean Charles
AU - Sacks, Frank
AU - Hermans, Michel P.
AU - Assmann, Gerd
AU - Brown, W. Virgil
AU - Ceska, Richard
AU - Chapman, M. John
AU - Dodson, Paul M.
AU - Fioretto, Paola
AU - Ginsberg, Henry N.
AU - Kadowaki, Takashi
AU - Lablanche, Jean Marc
AU - Marx, Nikolaus
AU - Plutzky, Jorge
AU - Reiner, Željko
AU - Rosenson, Robert S.
AU - Staels, Bart
AU - Stock, Jane K.
AU - Sy, Rody
AU - Wanner, Christoph
AU - Zambon, Alberto
AU - Zimmet, Paul
N1 - Funding Information:
Robert S. Rosenson, MD , has received funding from Abbott Laboratories, Anthera Pharmaceuticals, Inc., and AstraZeneca (research grant); serves on the Speakers' Bureau; receives honoraria payment from Abbott Laboratories and AstraZeneca; and has ownership interest and serves as a consultant/advisory board for LipoScience.
Funding Information:
Nikolaus Marx, MD , has received research grants from GlaxoSmithKline, Takeda, Boehringer Ingelheim, Novartis Pharmaceuticals Corporation, and Merck Sharp & Dohme; has received honoraria for advisory board membership from GlaxoSmithKline, Boehringer Ingelheim, Novo Nordisk, Merck Sharp & Dohme, and Sankyo; and has received honoraria for speaking from GlaxoSmithKline, Takeda Pharmaceuticals, Boehringer Ingelheim, BerlinChemie, and Merck Sharp & Dohme.
Funding Information:
Rody Sy, MD , has received research grants from Fournier Philippines, Pfizer Philippines, and Takeda Philippines; and has received honoraria for speaking from Merck Sharp & Dohme, Novartis Pharmaceuticals Corporation, Pfizer, Inc, Therapharma, sanofi-aventis, and Solvay Pharmaceuticals, Inc.
Funding Information:
W. Virgil Brown, MD , has received research grants from AstraZeneca, Abbott Laboratories, and Eli Lilly; and has received honoraria for speaking or consulting from AstraZeneca, Abbott Laboratories, Amgen, Inc., GlaxoSmithKline, Eli Lilly, Merck & Co., Inc., Merck/Schering-Plough, Pfizer, Inc, sanofi-aventis, and Solvay Pharmaceuticals, Inc.
Funding Information:
M. John Chapman, PhD, DSc , has received research funding from Merck & Co., Inc., Pfizer, and AstraZeneca; and has received sponsorship for presentation of educational conferences from these same companies.
Funding Information:
This work is funded by Solvay Pharmaceuticals, Inc.
PY - 2008/11/17
Y1 - 2008/11/17
N2 - Despite achieving targets for low-density lipoprotein (LDL) cholesterol, blood pressure, and glycemia in accordance with current standards of care, patients with dyslipidemia remain at high residual risk of vascular events. Atherogenic dyslipidemia, characterized by elevated triglycerides and low levels of high-density lipoprotein (HDL) cholesterol, often with elevated apolipoprotein B and non-HDL cholesterol, is common in patients with established cardiovascular disease (CVD), type 2 diabetes mellitus, or metabolic syndrome and contributes to both macrovascular and microvascular residual risk. However, atherogenic dyslipidemia is largely underdiagnosed and undertreated in clinical practice. The Residual Risk Reduction Initiative (R3i) was established to address this highly relevant clinical issue. The aims of this position paper are (1) to highlight evidence that atherogenic dyslipidemia is associated with residual macrovascular and microvascular risk in patients at high risk for CVD, despite current standards of care for dyslipidemia and diabetes; and (2) to recommend therapeutic intervention for reducing this residual vascular risk supported by evidence and expert consensus. Lifestyle modification with nutrition and exercise is an important, effective, and underutilized first step in reducing residual vascular risk. Therapeutic intervention aimed at achievement of all lipid targets is also often required. Combination lipid-modifying therapy, with the addition of niacin, a fibrate, or omega-3 fatty acids to statin therapy, increases the probability of achieving all lipid goals. Outcomes studies are in progress to evaluate whether these combination treatment strategies translate to a clinical benefit greater than that achieved with statins alone. The R3i highlights the need to address with lifestyle and/or pharmacotherapy the high level of residual risk of CVD events and microvascular complications among patients with dyslipidemia receiving therapy for high levels of LDL cholesterol and for diabetes in accordance with current standards of care.
AB - Despite achieving targets for low-density lipoprotein (LDL) cholesterol, blood pressure, and glycemia in accordance with current standards of care, patients with dyslipidemia remain at high residual risk of vascular events. Atherogenic dyslipidemia, characterized by elevated triglycerides and low levels of high-density lipoprotein (HDL) cholesterol, often with elevated apolipoprotein B and non-HDL cholesterol, is common in patients with established cardiovascular disease (CVD), type 2 diabetes mellitus, or metabolic syndrome and contributes to both macrovascular and microvascular residual risk. However, atherogenic dyslipidemia is largely underdiagnosed and undertreated in clinical practice. The Residual Risk Reduction Initiative (R3i) was established to address this highly relevant clinical issue. The aims of this position paper are (1) to highlight evidence that atherogenic dyslipidemia is associated with residual macrovascular and microvascular risk in patients at high risk for CVD, despite current standards of care for dyslipidemia and diabetes; and (2) to recommend therapeutic intervention for reducing this residual vascular risk supported by evidence and expert consensus. Lifestyle modification with nutrition and exercise is an important, effective, and underutilized first step in reducing residual vascular risk. Therapeutic intervention aimed at achievement of all lipid targets is also often required. Combination lipid-modifying therapy, with the addition of niacin, a fibrate, or omega-3 fatty acids to statin therapy, increases the probability of achieving all lipid goals. Outcomes studies are in progress to evaluate whether these combination treatment strategies translate to a clinical benefit greater than that achieved with statins alone. The R3i highlights the need to address with lifestyle and/or pharmacotherapy the high level of residual risk of CVD events and microvascular complications among patients with dyslipidemia receiving therapy for high levels of LDL cholesterol and for diabetes in accordance with current standards of care.
UR - http://www.scopus.com/inward/record.url?scp=56349154187&partnerID=8YFLogxK
U2 - 10.1016/j.amjcard.2008.10.002
DO - 10.1016/j.amjcard.2008.10.002
M3 - Article
C2 - 19068318
AN - SCOPUS:56349154187
SN - 0002-9149
VL - 102
SP - 1K-34K
JO - American Journal of Cardiology
JF - American Journal of Cardiology
IS - 10 SUPPL.
ER -