Genetic lecithin:cholesterol acyltransferase deficiency and cardiovascular disease.

Abstract:

:The lecithin:cholesterol acyltransferase (LCAT) enzyme is responsible for the synthesis of cholesteryl esters in human plasma and plays a critical role in high density lipoprotein (HDL) metabolism. Genetic LCAT deficiency is a rare metabolic disorder characterized by low HDL cholesterol levels. This paper reviews the genetic and biochemical features of LCAT deficiency, highlighting the absence of enhanced preclinical atherosclerosis in carriers, despite the remarkably low HDL cholesterol.

journal_name

Atherosclerosis

journal_title

Atherosclerosis

authors

Calabresi L,Simonelli S,Gomaraschi M,Franceschini G

doi

10.1016/j.atherosclerosis.2011.11.034

subject

Has Abstract

pub_date

2012-06-01 00:00:00

pages

299-306

issue

2

eissn

0021-9150

issn

1879-1484

pii

S0021-9150(11)01105-1

journal_volume

222

pub_type

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