Very low levels of HDL cholesterol and atherosclerosis, a variable relationship--a review of LCAT deficiency
- PMID: 22701329
- PMCID: PMC3373316 (VSports app下载)
- DOI: 10.2147/VHRM.S29985
VSports手机版 - Very low levels of HDL cholesterol and atherosclerosis, a variable relationship--a review of LCAT deficiency
Abstract (V体育2025版)
A number of epidemiological and clinical studies have demonstrated that plasma high-density lipoprotein (HDL) level is a strong inverse predictor of cardiovascular events. HDL is believed to retard the formation of atherosclerotic lesions by removing excess cholesterol from cells and preventing endothelial dysfunction. Lecithin cholesterol acyltransferase (LCAT) plays a central role in the formation and maturation of HDL, and in the intravascular stage of reverse cholesterol transport: a major mechanism by which HDL modulates the development and progression of atherosclerosis. A defect in LCAT function would be expected to enhance atherosclerosis, by interfering with the reverse cholesterol transport step. As such, one would expect to find more atherosclerosis and cardiovascular events in LCAT-deficient patients. But this relationship is not always evident VSports手机版. In this review, we describe contradictory reports in the literature about cardiovascular risks in this patient population. We discuss the paradoxical finding of severe HDL deficiency and an absence of subclinical atherosclerosis in LCAT-deficient patients, which has been used to reject the hypothesis that HDL level is important in the protection against atherosclerosis. Furthermore, to illustrate this paradoxical finding, we present a case study of one patient, referred for evaluation of global cardiovascular risk in the presence of a low HDL cholesterol level, who was diagnosed with LCAT gene mutations. .
Keywords: LCAT function; atherosclerosis; cardiovascular risk; high-density lipoprotein. V体育安卓版.
Figures
References
-
- Gordon DJ, Rifkind BM. High-density lipoprotein – the clinical implications of recent studies. N Engl J Med. 1989;321(19):1311–1316. - PubMed
-
- Barter P, Gotto AM, LaRosa JC, et al. Hdl cholesterol, very low levels of ldl cholesterol, and cardiovascular events. N Engl J Med. 2007;357(13):1301–1310. - PubMed (VSports app下载)
-
- Czarnecka H, Yokoyama S. Regulation of cellular cholesterol efflux by lecithin: Cholesterol acyltransferase reaction through nonspecific lipid exchange. J Biol Chem. 1996;271(4):2023–2028. - PubMed
-
- Kuivenhoven JA, Pritchard H, Hill J, Frohlich J, Assmann G, Kastelein J. The molecular pathology of lecithin: Cholesterol acyltransferase (lcat) deficiency syndromes. J Lipid Res. 1997;38(2):191–205. - V体育2025版 - PubMed
-
- Calabresi L, Pisciotta L, Costantin A, et al. The molecular basis of lecithin: Cholesterol acyltransferase deficiency syndromes: A comprehensive study of molecular and biochemical findings in 13 unrelated italian families. Arterioscler Thromb Vasc Biol. 2005;25(9):1972–1978. - PubMed
Publication types
- Actions (VSports手机版)
MeSH terms
- "VSports手机版" Actions
- "V体育安卓版" Actions
- Actions (VSports最新版本)
- "V体育安卓版" Actions
- "VSports最新版本" Actions
- Actions (V体育官网入口)
- "VSports" Actions
- "VSports app下载" Actions
- Actions (VSports app下载)
Substances
- "V体育官网入口" Actions
LinkOut - more resources
Full Text Sources (V体育ios版)
Medical
Research Materials
V体育ios版 - Miscellaneous
