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High-density lipoprotein infusion therapy: A review
H Bryan Brewer1, Ernst J Schaefer2, Borek Foldyna3
1HDL Therapeutics, Vero Beach, FL, USA (Dr Brewer).
Insights
High-density lipoprotein (HDL) infusions show potential for atherosclerosis regression, but results vary. Differences in HDL preparations, patient populations, and assessment methods may explain inconsistent outcomes in clinical trials.
Area of Science:
- Cardiovascular Medicine
- Biochemistry
- Medical Imaging
Background:
- Increased cholesterol-rich, non-calcified atheromas predict myocardial infarction better than traditional markers.
- Low high-density lipoprotein (HDL) cholesterol is an independent risk factor for coronary artery disease (CAD).
- Small, lipid-poor preβ-1 HDL particles are effective in cellular cholesterol efflux.
Purpose of the Study:
- To review animal and human studies on HDL infusion therapy for atherosclerosis regression.
- To explore reasons for variable outcomes in HDL infusion studies.
Main Methods:
- Review of animal studies demonstrating HDL's effect on aortic atherosclerosis.
- Analysis of human clinical trials using HDL mimetics and native HDL infusions.
- Examination of studies employing intravascular ultrasound and computed coronary angiography for atherosclerosis assessment.
Main Results:
- HDL infusions reduced aortic atherosclerosis in animal models.
- Some human studies with HDL mimetics or complexes yielded negative results for coronary atherosclerosis progression.
- A study using autologous delipidated HDL infusions showed significant regression of coronary atheroma in familial hypercholesterolemic patients.
Conclusions:
- HDL infusion therapy shows promise for atherosclerosis regression, particularly with autologous delipidated HDL.
- Variability in results may stem from differences in HDL preparations, patient selection, and imaging assessment techniques.
- Further research is needed to optimize HDL-based therapies for cardiovascular disease.
Abstract:
Increased cholesterol-rich, low-density, non-calcified atheromas as assessed by computer coronary tomography angiography analyses have been shown to predict myocardial infarction significantly better than coronary artery calcium score or the presence of obstructive coronary artery disease (CAD) as evaluated with standard coronary angiography. Low serum high-density lipoprotein (HDL) cholesterol values are an independent risk factor for CAD. Very small, lipid-poor preβ-1 HDL particles have been shown to be most effective in promoting cellular cholesterol efflux. HDL infusions have been documented to reduce aortic atherosclerosis in cholesterol-fed animal models. However, human studies using infusions of either the HDL mimetic containing recombinant apolipoprotein (apo) A-I Milano or Cerenis Compound-001 with native recombinant apoA-I have been mainly negative in promoting coronary atherosclerosis progression as assessed by intravascular ultrasound. In contrast, a study using 7 weekly infusions of autologous delipidated HDL in six homozygous familial hypercholesterolemic patients was effective in promoting significant regression of low-density non-calcified coronary atheroma regression as assessed by computed coronary angiography. This therapy has received Food and Drug Administration approval. Commonwealth Serum Laboratories has carried out a large clinical endpoint trial using an HDL complex (native apoA-I with phospholipid), and the results were negative. Our purpose is to review animal and human studies using various forms of HDL infusion therapy to promote regression of atherosclerosis. In our view, differences in results may be due to: 1) the HDL preparations used, 2) the subjects studied, and 3) the methods used to assess coronary atherosclerosis.
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