Evidence of a Polygenic Origin of Extreme High-Density Lipoprotein Cholesterol Levels
Author(s) -
Mohammad Mahdi Motazacker,
Jorge Peter,
M. Treskes,
Carol C. Shoulders,
Jan Albert Kuivenhoven,
G. Kees Hovingh
Publication year - 2013
Publication title -
arteriosclerosis thrombosis and vascular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.007
H-Index - 270
eISSN - 1524-4636
pISSN - 1079-5642
DOI - 10.1161/atvbaha.113.301505
Subject(s) - nonsynonymous substitution , genetics , biology , population , odds ratio , single nucleotide polymorphism , medicine , gene , genotype , environmental health , genome
There are several known monogenic causes of high and low high-density lipoprotein cholesterol (HDL-C) levels, but traditional sequencing studies have had limited success in identifying mutations in the majority of individuals with extreme HDL-C levels. The aim of this study was to assess the power of a targeted high-throughput sequencing strategy to elucidate the genetic basis of extreme HDL-C phenotypes.
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