Publication:
Effects of lecithin: Cholesterol acyltransferase genotypes, enzyme levels, and activity on high-density lipoprotein levels

dc.contributor.authorEREN, FATİH
dc.contributor.authorsAgirbasli, Deniz; Cirakoglu, Beyazit; Eren, Fatih; Sumerkan, Mutlu; Aksoy, Sukru; Aral, Cenk; Agirbasli, Mehmet
dc.date.accessioned2022-03-12T17:53:26Z
dc.date.accessioned2026-01-10T20:51:49Z
dc.date.available2022-03-12T17:53:26Z
dc.date.issued2011
dc.description.abstractBACKGROUND: Lecithin:cholesterol acyltransferase (LCAT) is one of the key enzymes controlling cholesterol homeostasis and plays a primary role in high-density lipoprotein cholesterol (HDL-C) maturation. OBJECTIVE: The aim of our study was to evaluate the effects of LCAT gene polymorphisms 511C/T (exon4), 4886C/T (rs5923), and 608C/T (rs5922) on LCAT enzyme level, activity, and HDL-C levels. METHODS: The study population was selected from consecutive subjects with low (<35 mg/dL) and high HDL-C levels (>65 mg/dL) seen in our lipid clinic. LCAT polymorphisms were analyzed with a restriction fragment length polymorphism assay. LCAT activity and levels were measured by colorimetric enzymatic and enzyme-linked immunoassay methods, respectively. RESULTS: The 4886C/T polymorphism was the most commonly observed variant of LCAT gene. T-allele frequencies in subjects with low (n = 50) and high (n = 50) HDL-C were 0.54 and 0.37, respectively (P = .019). genotype was more common among low HDL-C group (30% vs 14%, P = .05). The effects of LCAT enzyme appeared to depend on the HDL-C level. In subjects with low HDL-C, LCAT enzyme levels correlated positively with body mass index (P < .001, r = 0.544), HDL-C (P = .006, r = 0.404), triglycerides (P = .001, r = 0.487), total cholesterol (P < .001, r = 0.541), and low-density lipoprotein-cholesterol (P = .001, r = 0.477) levels. LCAT activity correlated positively with fasting glucose levels (P = .008, r = 0.390). CONCLUSION: LCAT genotype, enzyme level, and activity modulate HDL-C metabolism, particularly among subjects with low HDL-C levels. (C) 2011 National Lipid Association. All rights reserved.
dc.identifier.doi10.1016/j.jacl.2011.02.008
dc.identifier.eissn1876-4789
dc.identifier.issn1933-2874
dc.identifier.pubmed21600519
dc.identifier.urihttps://hdl.handle.net/11424/230462
dc.identifier.wosWOS:000290745600005
dc.language.isoeng
dc.publisherELSEVIER SCIENCE INC
dc.relation.ispartofJOURNAL OF CLINICAL LIPIDOLOGY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectCoronary artery disease
dc.subjectEnzyme activity
dc.subjectEnzyme level
dc.subjectGenetic polymorphisms
dc.subjectHigh-density lipoprotein-cholesterol
dc.subjectLecithin:cholesterol acyltransferase
dc.subjectCORONARY-ARTERY-DISEASE
dc.subjectHEART-DISEASE
dc.subjectMYOCARDIAL-INFARCTION
dc.subjectTURKISH POPULATION
dc.subjectHDL3 SUBFRACTIONS
dc.subjectRISK
dc.subjectGENE
dc.subjectATHEROSCLEROSIS
dc.subjectPOLYMORPHISMS
dc.subjectLCAT
dc.titleEffects of lecithin: Cholesterol acyltransferase genotypes, enzyme levels, and activity on high-density lipoprotein levels
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage158
oaire.citation.issue3
oaire.citation.startPage152
oaire.citation.titleJOURNAL OF CLINICAL LIPIDOLOGY
oaire.citation.volume5

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