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Compromised LCAT Function Is Associated With Increased Atherosclerosis
Author(s) -
G. Kees Hovingh,
Barbara A. Hutten,
Adriaan G. Holleboom,
Wilma Petersen,
Patrick Rol,
Anton F. H. Stalenhoef,
Aeilko H. Zwinderman,
Eric de Groot,
John J.P. Kastelein,
Jan Albert Kuivenhoven
Publication year - 2005
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.105.540427
Subject(s) - medicine , endocrinology , heterozygote advantage , cholesterol , triglyceride , apolipoprotein b , lecithin—cholesterol acyltransferase , lecithin , sterol o acyltransferase , lipoprotein , allele , gene , biology , genetics , biochemistry
Prospective epidemiological studies have shown that low plasma levels of HDL cholesterol (HDL-C) are associated with an increased risk for cardiovascular disease (CVD). Despite nearly 40 years of research, however, it is unclear whether this also holds true for individuals with severely reduced levels of HDL-C due to mutations in the lecithin:cholesterol acyltransferase (LCAT) gene. Better insight into CVD risk in these individuals may provide clues toward the potential of LCAT as a pharmaceutical target to raise HDL-C levels.

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