| Literature DB >> 25561459 |
Ruud S Kootte1, Loek P Smits1, Fleur M van der Valk1, Jean-Louis Dasseux2, Constance H Keyserling2, Ronald Barbaras2, John F Paolini2, Raul D Santos3, Theo H van Dijk4, Geesje M Dallinga-van Thie1, Aart J Nederveen5, Willem J M Mulder1, G Kees Hovingh1, John J P Kastelein1, Albert K Groen4, Erik S Stroes1.
Abstract
Reverse cholesterol transport (RCT) contributes to the anti-atherogenic effects of HDL. Patients with the orphan disease, familial hypoalphalipoproteinemia (FHA), are characterized by decreased tissue cholesterol removal and an increased atherogenic burden. We performed an open-label uncontrolled proof-of-concept study to evaluate the effect of infusions with a human apoA-I-containing HDL-mimetic particle (CER-001) on RCT and the arterial vessel wall in FHA. Subjects received 20 infusions of CER-001 (8 mg/kg) during 6 months. Efficacy was assessed by measuring (apo)lipoproteins, plasma-mediated cellular cholesterol efflux, fecal sterol excretion (FSE), and carotid artery wall dimension by MRI and artery wall inflammation by (18)F-fluorodeoxyglucose-positron emission tomography/computed tomography scans. We included seven FHA patients: HDL-cholesterol (HDL-c), 13.8 [1.8-29.1] mg/dl; apoA-I, 28.7 [7.9-59.1] mg/dl. Following nine infusions in 1 month, apoA-I and HDL-c increased directly after infusion by 27.0 and 16.1 mg/dl (P = 0.018). CER-001 induced a 44% relative increase (P = 0.018) in in vitro cellular cholesterol efflux with a trend toward increased FSE (P = 0.068). After nine infusions of CER-001, carotid mean vessel wall area decreased compared with baseline from 25.0 to 22.8 mm(2) (P = 0.043) and target-to-background ratio from 2.04 to 1.81 (P = 0.046). In FHA-subjects, CER-001 stimulates cholesterol mobilization and reduces artery wall dimension and inflammation, supporting further evaluation of CER-001 in FHA patients.Entities:
Keywords: apolipoprotein A-I; familial hypoalphalipoproteinemia; reverse cholesterol transport
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Year: 2015 PMID: 25561459 PMCID: PMC4340317 DOI: 10.1194/jlr.M055665
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922