Low-density lipoprotein levels and not mutation status predict Intima-media thickness in familial hypercholesterolemia
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Abstract
Background Intima-media thickness (IMT) is a well-described marker of cardiovascular disease. In this study we aim to determine whether low-density lipoprotein (LDL) levels and disease-related mutation status can predict IMT in patients with severe familial hypercholesterolemia (FH) referred for or on LDL apheresis. Methods Genetic screening, lipid profile testing, and IMT measurements were performed on a series of 33 severe FH patients (19 homozygous) on LDL apheresis treatments (LDL 447 ± 151 mg/dL, age range 6-60 years). Data were then compared with literature IMT-LDL data for normal subjects, mild FH patients, and severe FH patients (18, 41, and 6 studies, respectively). Results Age-adjusted IMT was linearly related to LDL levels over a wide range of values (<500 mg/dL), except for the severe FH no-apheresis cohort. Alternatively, our severe FH population (mostly on apheresis) did follow the mild FH/control age-adjusted IMT-LDL relation. Conclusions In severe FH, measuring LDL levels is more predictive of increased IMT than genetic screening. © 2014 Elsevier Inc. All rights reserved.
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Adolescent, Adult, Age factors, Apolipoproteins e, Biological markers, Blood component removal, Carotid artery diseases, Carotid intima-media thickness, Case-control studies, Child, Dna mutational analysis, Genetic predisposition to disease, Genetic testing, Heterozygote, Homozygote, Humans, Hyperlipoproteinemia type ii, Lipoproteins, ldl, Middle aged, Mutation, Phenotype, Predictive value of tests, Receptors, ldl, Risk factors, Severity of illness index, Young adult