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LDL-Cholesterol: Standards of Treatment 2016: A German Perspective
Winfried März1,2,3,4, Hubert Scharnagl5, Ioanna Gouni-Berthold6
1Society for the Prevention of Cardiovascular Disease e.V. (DACH), Schulterblatt 120, 20357, Hamburg, Germany. winfried.maerz@synlab.com.
Insights
Lowering low-density lipoprotein cholesterol (LDL-C) is crucial for preventing atherosclerosis, with treatment intensity based on cardiovascular risk. PCSK9 antibodies offer a potent option for patients not meeting LDL-C targets.
Area of Science:
- Cardiology
- Pharmacology
- Preventive Medicine
Background:
- Decreasing low-density lipoprotein cholesterol (LDL-C) is a proven strategy for atherosclerosis prevention and treatment.
- Cardiovascular risk stratification dictates the intensity and benefit of lipid-lowering pharmacotherapy.
- Treatment targets for LDL-C vary based on patient risk, ranging from <115 mg/dl for low/moderate risk to <70 mg/dl for very high risk.
Purpose of the Study:
- To review current guidelines and therapeutic options for managing hypercholesterolemia.
- To evaluate the role and efficacy of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors.
- To propose the use of PCSK9 inhibitors in specific patient groups, especially those at very high cardiovascular risk.
Main Methods:
- Review of current clinical guidelines for hypercholesterolemia management.
- Analysis of available lipid-lowering pharmacotherapies, including statins, ezetimibe, and PCSK9 inhibitors.
- Appraisal of PCSK9 antibodies based on their efficacy, tolerability, and potential clinical impact.
Main Results:
- Lifestyle modifications are fundamental, but pharmacotherapy is often necessary to achieve LDL-C goals.
- Statins are first-line therapy; ezetimibe and PCSK9 inhibitors are valuable alternatives or additions.
- PCSK9 antibodies demonstrate significant LDL-C reduction (50-60%) and are generally well-tolerated.
Conclusions:
- Hypercholesterolemia management requires individualized treatment strategies based on cardiovascular risk.
- PCSK9 inhibitors represent a significant advancement, particularly for high-risk patients refractory to other therapies.
- Further research is ongoing to confirm the clinical endpoint benefits of PCSK9 antibodies in large-scale trials.
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.
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