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Updated: Jun 1, 2026

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
Published on: January 28, 2021
Lipoprotein abnormalities in patients with atherosclerotic renovascular disease
Elzbieta Nowakowska Fortuna1, Hans Herlitz, Aso Saeed
1Department of Molecular and Clinical Medicine/Nephrology, Institute of Medicine, The Sahlgrenska Academy at the University of Gothenburg, Sweden.
Insights
Atherosclerotic renovascular disease patients exhibit elevated levels of specific lipoproteins, indicating an increased risk for cardiovascular events. These findings highlight potential targets for managing atherosclerosis in ARVD.
Area of Science:
- Cardiovascular Medicine
- Lipid Metabolism
- Renal Artery Disease
Background:
- Atherosclerotic renovascular disease (ARVD) patients face a high risk of cardiovascular mortality.
- Characterizing lipoprotein (Lp) subclasses is crucial for understanding ARVD pathophysiology.
Purpose of the Study:
- To investigate apolipoprotein (Apo)-defined lipoprotein subclass abnormalities in ARVD patients.
- To assess the impact of candesartan treatment on these lipoprotein profiles.
Main Methods:
- Baseline measurements in 42 ARVD patients post-renal angioplasty, all on statins.
- Comparison with 20 age-matched healthy controls.
- Randomization to candesartan or non-renin-angiotensin-aldosterone system inhibitors for 11 months.
Main Results:
- ARVD patients showed significantly elevated ApoC-III, LpB:C:E, and total ApoC-III-containing lipoproteins versus controls.
- Plasma renin activity was independently associated with baseline ApoC-III levels.
- Candesartan treatment did not resolve these lipoprotein abnormalities.
Conclusions:
- Statin-treated ARVD patients present an atherogenic lipoprotein profile.
- Elevated ApoC-III-containing, triglyceride-rich lipoproteins may accelerate atherosclerotic disease progression.
Background:
Patients with atherosclerotic renovascular disease (ARVD) have a high risk of cardiovascular death. The primary aim was to characterize abnormalities in apolipoprotein (Apo)-defined lipoprotein (Lp) subclasses in patients with ARVD.
Methods:
Baseline measurements were performed on 42 patients with ARVD 4 weeks after renal angioplasty (PTRA). All patients were on statin treatment. Twenty age-matched healthy subjects without medications served as controls. Subsequently, patients were randomized to treatment with either candesartan (n = 21), or antihypertensive treatment without inhibitors of the renin-angiotensin-aldosterone system (n = 21) and followed for 11 months.
Results:
At baseline, ApoC-III (12.7 ± 4.6 vs. 8.8 ± 2.6 (SD) mg/dl, p < 0.05), LpB:C:E (13.3 ± 5.4 vs. 8.4 ± 4.3 mg/dl, p < 0.05), and the sum of ApoC-III-containing lipoproteins, i.e. LpB:C + LpB:C:E + LpA-II:B:C:D:E (46 ± 15 vs. 37 ± 8 mg/dl, p < 0.05), were significantly elevated in ARVD patients versus healthy controls. Multiple regression analyses showed that only plasma renin activity was independently associated with ApoC-III levels at baseline (p < 0.05, r = 0.74). Treatment with candesartan did not correct abnormalities.
Conclusions:
Patients with ARVD treated with statins have an atherogenic lipoprotein profile characterized by elevated levels of ApoC-III-containing, triglyceride-rich lipoproteins that could accelerate atherosclerotic disease.
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