Individualized lipid-lowering therapy to further reduce residual cardiovascular risk. Issue 169 (May 2017)
- Record Type:
- Journal Article
- Title:
- Individualized lipid-lowering therapy to further reduce residual cardiovascular risk. Issue 169 (May 2017)
- Main Title:
- Individualized lipid-lowering therapy to further reduce residual cardiovascular risk
- Authors:
- Weingärtner, Oliver
Lütjohann, Dieter
Plösch, Torsten
Elsässer, Albrecht - Abstract:
- Highlights: Optimal lipid-lowering therapy is essential for patients with known cardiovascular diseases. This review summarizes current endpoint studies of lipid-lowering drugs and suggests an individual approach based on patient characteristics. The "Oldenburg Lipid Therapy Path" is a suggestion for a model to guide the use of combined lipid-lowering therapy. Abstract: Hypercholesterolemia is a major risk factor for cardiovascular diseases. Serum cholesterol concentrations are regulated by enteral absorption, biliary secretion, and hepatic synthesis. Statins inhibit the rate-limiting enzyme of cholesterol synthesis, HMG-CoA-reductase, and reduce serum cholesterol concentrations as well as cardiovascular morbidity and mortality. Some studies indicate that patients with high baseline cholesterol absorption may show only a small response to statin treatment in terms of cholesterol lowering. Data from genetic association studies and from the IMPROVE-IT trial show that reducing intestinal cholesterol absorption via NCP1L1 further reduces cardiovascular risk. However, some patients do not attain LDL-cholesterol targets on combination therapy. For these patients PCSK9-antibody treatment and lipid-apheresis are options to be considered. This article reviews the current literature on this issue and suggests 'individualized lipid-lowering therapy' as an approach to optimize and personalize lipid-lowering treatment of patients with hypercholesterolemia to further reduce residualHighlights: Optimal lipid-lowering therapy is essential for patients with known cardiovascular diseases. This review summarizes current endpoint studies of lipid-lowering drugs and suggests an individual approach based on patient characteristics. The "Oldenburg Lipid Therapy Path" is a suggestion for a model to guide the use of combined lipid-lowering therapy. Abstract: Hypercholesterolemia is a major risk factor for cardiovascular diseases. Serum cholesterol concentrations are regulated by enteral absorption, biliary secretion, and hepatic synthesis. Statins inhibit the rate-limiting enzyme of cholesterol synthesis, HMG-CoA-reductase, and reduce serum cholesterol concentrations as well as cardiovascular morbidity and mortality. Some studies indicate that patients with high baseline cholesterol absorption may show only a small response to statin treatment in terms of cholesterol lowering. Data from genetic association studies and from the IMPROVE-IT trial show that reducing intestinal cholesterol absorption via NCP1L1 further reduces cardiovascular risk. However, some patients do not attain LDL-cholesterol targets on combination therapy. For these patients PCSK9-antibody treatment and lipid-apheresis are options to be considered. This article reviews the current literature on this issue and suggests 'individualized lipid-lowering therapy' as an approach to optimize and personalize lipid-lowering treatment of patients with hypercholesterolemia to further reduce residual cardiovascular risk. … (more)
- Is Part Of:
- Journal of steroid biochemistry and molecular biology. Issue 169(2017)
- Journal:
- Journal of steroid biochemistry and molecular biology
- Issue:
- Issue 169(2017)
- Issue Display:
- Volume 169, Issue 169 (2017)
- Year:
- 2017
- Volume:
- 169
- Issue:
- 169
- Issue Sort Value:
- 2017-0169-0169-0000
- Page Start:
- 198
- Page End:
- 201
- Publication Date:
- 2017-05
- Subjects:
- Cholesterol -- Individualized lipid-lowering therapy -- Cardiovascular risk
Steroid hormones -- Periodicals
Biochemistry -- Periodicals
Hormones -- Periodicals
Molecular Biology -- Periodicals
Hormones stéroïdes -- Périodiques
Steroid hormones
Periodicals
572.579 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09600760 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jsbmb.2016.05.016 ↗
- Languages:
- English
- ISSNs:
- 0960-0760
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5066.850010
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1131.xml