LDL-Cholesterol: Standards of Treatment 2016: A German Perspective

Standard

LDL-Cholesterol: Standards of Treatment 2016: A German Perspective. / März, Winfried; Scharnagl, Hubert; Gouni-Berthold, Ioanna; Silbernagel, Günther; Dressel, Alexander; Grammer, Tanja B; Landmesser, Ulf; Dieplinger, Hans; Windler, Eberhard; Laufs, Ulrich.

in: AM J CARDIOVASC DRUG, Jahrgang 16, Nr. 5, 10.2016, S. 323-336.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ReviewForschung

Harvard

März, W, Scharnagl, H, Gouni-Berthold, I, Silbernagel, G, Dressel, A, Grammer, TB, Landmesser, U, Dieplinger, H, Windler, E & Laufs, U 2016, 'LDL-Cholesterol: Standards of Treatment 2016: A German Perspective', AM J CARDIOVASC DRUG, Jg. 16, Nr. 5, S. 323-336. https://doi.org/10.1007/s40256-016-0179-y

APA

März, W., Scharnagl, H., Gouni-Berthold, I., Silbernagel, G., Dressel, A., Grammer, T. B., Landmesser, U., Dieplinger, H., Windler, E., & Laufs, U. (2016). LDL-Cholesterol: Standards of Treatment 2016: A German Perspective. AM J CARDIOVASC DRUG, 16(5), 323-336. https://doi.org/10.1007/s40256-016-0179-y

Vancouver

März W, Scharnagl H, Gouni-Berthold I, Silbernagel G, Dressel A, Grammer TB et al. LDL-Cholesterol: Standards of Treatment 2016: A German Perspective. AM J CARDIOVASC DRUG. 2016 Okt;16(5):323-336. https://doi.org/10.1007/s40256-016-0179-y

Bibtex

@article{f00b7372296d4d20bf26d289b1a95357,
title = "LDL-Cholesterol: Standards of Treatment 2016: A German Perspective",
abstract = "Decreasing low-density lipoprotein cholesterol (LDL-C) is one of the few established and proven principles for the prevention and treatment of atherosclerosis. The higher the individual cardiovascular risk, the higher the benefit of lipid-lowering pharmacotherapy. Therefore, treatment options are chosen based on a patient's total cardiovascular risk. The latter depends not only on the levels of LDL-C but also on the presence of cardiovascular disease (CVD) and on the number and severity of other risk factors. Current guidelines recommend the lowering of LDL-C to 115 mg/dl (3 mmol/l) in patients with low and moderate risk. The LDL-C treatment target is <100 mg/dl (2.6 mmol/l) for patients at high risk and <70 mg/dl (1.8 mmol/l) for patients at very high risk. Although lifestyle measures remain a fundamental part of treatment, many patients require drug therapy to achieve their LDL-C targets. Statins are the drugs of choice, with other options including ezetimibe and the newly available monoclonal antibodies against PCSK9 (proprotein convertase subtilisin/kexin type 9). In some cases, bile acid-binding sequestrants and fibrates can also be considered. Nicotinic acid is no longer available in Germany. PCSK9 antibodies decrease LDL-C about 50-60 % and are well tolerated. Their effects on clinical endpoints are being investigated in large randomized trials. The aim of the present review is to summarize the current guidelines and treatment options for hypercholesterolemia. Moreover, we provide an appraisal of PCSK9 antibodies and propose their use in selected patient populations, particularly in those at very high cardiovascular risk whose LDL-C levels under maximally tolerated lipid-lowering therapy are significantly over their treatment target. ",
keywords = "Antibodies, Monoclonal/therapeutic use, Anticholesteremic Agents/therapeutic use, Cardiovascular Diseases/blood, Cholesterol, LDL/blood, Germany, Humans, Hypercholesterolemia/blood, Proprotein Convertase 9/metabolism, Randomized Controlled Trials as Topic, Risk Factors",
author = "Winfried M{\"a}rz and Hubert Scharnagl and Ioanna Gouni-Berthold and G{\"u}nther Silbernagel and Alexander Dressel and Grammer, {Tanja B} and Ulf Landmesser and Hans Dieplinger and Eberhard Windler and Ulrich Laufs",
year = "2016",
month = oct,
doi = "10.1007/s40256-016-0179-y",
language = "English",
volume = "16",
pages = "323--336",
journal = "AM J CARDIOVASC DRUG",
issn = "1175-3277",
publisher = "Adis International Ltd",
number = "5",

}

RIS

TY - JOUR

T1 - LDL-Cholesterol: Standards of Treatment 2016: A German Perspective

AU - März, Winfried

AU - Scharnagl, Hubert

AU - Gouni-Berthold, Ioanna

AU - Silbernagel, Günther

AU - Dressel, Alexander

AU - Grammer, Tanja B

AU - Landmesser, Ulf

AU - Dieplinger, Hans

AU - Windler, Eberhard

AU - Laufs, Ulrich

PY - 2016/10

Y1 - 2016/10

N2 - Decreasing low-density lipoprotein cholesterol (LDL-C) is one of the few established and proven principles for the prevention and treatment of atherosclerosis. The higher the individual cardiovascular risk, the higher the benefit of lipid-lowering pharmacotherapy. Therefore, treatment options are chosen based on a patient's total cardiovascular risk. The latter depends not only on the levels of LDL-C but also on the presence of cardiovascular disease (CVD) and on the number and severity of other risk factors. Current guidelines recommend the lowering of LDL-C to 115 mg/dl (3 mmol/l) in patients with low and moderate risk. The LDL-C treatment target is <100 mg/dl (2.6 mmol/l) for patients at high risk and <70 mg/dl (1.8 mmol/l) for patients at very high risk. Although lifestyle measures remain a fundamental part of treatment, many patients require drug therapy to achieve their LDL-C targets. Statins are the drugs of choice, with other options including ezetimibe and the newly available monoclonal antibodies against PCSK9 (proprotein convertase subtilisin/kexin type 9). In some cases, bile acid-binding sequestrants and fibrates can also be considered. Nicotinic acid is no longer available in Germany. PCSK9 antibodies decrease LDL-C about 50-60 % and are well tolerated. Their effects on clinical endpoints are being investigated in large randomized trials. The aim of the present review is to summarize the current guidelines and treatment options for hypercholesterolemia. Moreover, we provide an appraisal of PCSK9 antibodies and propose their use in selected patient populations, particularly in those at very high cardiovascular risk whose LDL-C levels under maximally tolerated lipid-lowering therapy are significantly over their treatment target.

AB - Decreasing low-density lipoprotein cholesterol (LDL-C) is one of the few established and proven principles for the prevention and treatment of atherosclerosis. The higher the individual cardiovascular risk, the higher the benefit of lipid-lowering pharmacotherapy. Therefore, treatment options are chosen based on a patient's total cardiovascular risk. The latter depends not only on the levels of LDL-C but also on the presence of cardiovascular disease (CVD) and on the number and severity of other risk factors. Current guidelines recommend the lowering of LDL-C to 115 mg/dl (3 mmol/l) in patients with low and moderate risk. The LDL-C treatment target is <100 mg/dl (2.6 mmol/l) for patients at high risk and <70 mg/dl (1.8 mmol/l) for patients at very high risk. Although lifestyle measures remain a fundamental part of treatment, many patients require drug therapy to achieve their LDL-C targets. Statins are the drugs of choice, with other options including ezetimibe and the newly available monoclonal antibodies against PCSK9 (proprotein convertase subtilisin/kexin type 9). In some cases, bile acid-binding sequestrants and fibrates can also be considered. Nicotinic acid is no longer available in Germany. PCSK9 antibodies decrease LDL-C about 50-60 % and are well tolerated. Their effects on clinical endpoints are being investigated in large randomized trials. The aim of the present review is to summarize the current guidelines and treatment options for hypercholesterolemia. Moreover, we provide an appraisal of PCSK9 antibodies and propose their use in selected patient populations, particularly in those at very high cardiovascular risk whose LDL-C levels under maximally tolerated lipid-lowering therapy are significantly over their treatment target.

KW - Antibodies, Monoclonal/therapeutic use

KW - Anticholesteremic Agents/therapeutic use

KW - Cardiovascular Diseases/blood

KW - Cholesterol, LDL/blood

KW - Germany

KW - Humans

KW - Hypercholesterolemia/blood

KW - Proprotein Convertase 9/metabolism

KW - Randomized Controlled Trials as Topic

KW - Risk Factors

U2 - 10.1007/s40256-016-0179-y

DO - 10.1007/s40256-016-0179-y

M3 - SCORING: Review article

C2 - 27430233

VL - 16

SP - 323

EP - 336

JO - AM J CARDIOVASC DRUG

JF - AM J CARDIOVASC DRUG

SN - 1175-3277

IS - 5

ER -