1. Myocardial infarction in a 36-year-old man with combined ABCA1 and APOA-1 deficiency.
- Author
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van Capelleveen JC, Kootte RS, Hovingh GK, and Bochem AE
- Subjects
- Adult, Humans, Male, ATP Binding Cassette Transporter 1 deficiency, Apolipoprotein A-I deficiency, Lipoproteins, HDL metabolism, Mutation, Myocardial Infarction genetics, Myocardial Infarction metabolism
- Abstract
In this report, we present a patient who suffered from a myocardial infarction at an extremely young age. The only remarkable finding in the risk factor workup was a near undetectable high-density lipoprotein (HDL)-cholesterol plasma level (0.09 mmol/L). Genetic analysis of key genes involved in HDL metabolism resulted in the discovery of 2 very rare mutations in the ABCA1 and APOA1 genes. We discuss the effects of these mutations on HDL metabolism and reverse cholesterol transport and interpret these findings in relation to the extensive atherosclerosis at a very young age in this patient., (Copyright © 2015 National Lipid Association. Published by Elsevier Inc. All rights reserved.)
- Published
- 2015
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