LPL, lipoprotein lipase, 4023

N. diseases: 290; N. variants: 116
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Influence of lipoprotein lipase serine 447 stop polymorphism on tracking of triglycerides and HDL cholesterol from childhood to adulthood and familial risk of coronary artery disease: the Bogalusa heart study. 11730816 2001
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The LPL polymorphism contributed to the severity of coronary disease in patients with MS and recent ACS. 29412239 2018
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Functional significance of lipoprotein lipase HindIII polymorphism associated with the risk of coronary artery disease. 18242618 2008
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The S447X polymorphism of lipoprotein lipase: effect on the incidence of premature coronary disease and on plasma lipids. 17533471 2007
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease. The Regress Study Group. 9550358 1998
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Two common coding sequence mutations of lipoprotein lipase (serine447-ter, producing a carboxy terminal truncation; and asp9-asn variants) were studied in 329 Caucasian subjects, of whom 243 had angiographic features of premature atheroscelerosis (220 with coronary artery disease; 23 with coronary and peripheral artery disease). 8835323 1995
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 Biomarker disease BEFREE Associations for lipoprotein lipase and peroxisome proliferator-activated receptor-gamma gene and coronary artery disease in an Indian population. 20430250 2010
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE LPL Pvull rare allele homozygote status seems to be beneficial with more favorable lipid changes and protection against CHD. 16419488 2005
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 Biomarker disease BEFREE We review the evidence for the role of apolipoprotein E, lipoprotein lipase and interleukin-6 in CHD and their interaction with smoking (an environmental risk). 12542551 2003
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The LPL S447X variant tended to be associated with lower TG and higher HDL-C levels, and lower risk of CHD in all 3 cohorts. 19185650 2009
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Genetic variants of the lipoprotein lipase gene have been associated with dyslipidemia and coronary artery disease. 10974229 2000
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The multivariate model included 512 men with coronary artery disease from the REGRESS study who were completely genotyped for eight polymorphisms selected in the univariate procedure (ie, APOA1 G(-75)A, ABCA1 C(-477)T, ABCA1 G1051A, APOC3 T3206G, APOE Arg158Cys, LIPC C(-514)T, LPL Asn291Ser and LPL Ser447Stop). 15657615 2005
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease. 11683775 2001
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Our results suggest that the LPL gene is involved in the determination of lipoprotein profiles, the predisposition to CHD, and the severity of atherosclerosis. 8576640 1995
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Lipoprotein lipase gene mutations in coronary artery disease. 9627528 1998
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Relative contribution of low-density lipoprotein receptor and lipoprotein lipase gene mutations to angiographically assessed coronary artery disease among French Canadians. 9708657 1998
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Novel LPL mutation (L303F) found in a patient associated with coronary artery disease and severe systemic atherosclerosis. 12641539 2003
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 Biomarker disease BEFREE Synergistic effect between lipoprotein lipase and apolipoprotein C3 genes in determining the severity of coronary artery disease. 23377670 2013
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The LPL Ser447Stop (S447X) allele is associated with anti-atherogenic lipid profiles and a modest reduction in risk for coronary disease. 16822320 2006
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Lipoprotein lipase gene PvuII polymorphism serum lipids and risk for coronary artery disease: meta-analysis. 17473385 2007
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Lack of association of lipoprotein lipase gene polymorphisms with coronary artery disease in the Saudi Arab population. 12708905 2003
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Regulatory mutations in the human lipoprotein lipase gene in patients with familial combined hyperlipidemia and coronary artery disease. 9017514 1996
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE The entire coding and boundary regions of LPL and HTGL genes were analyzed by direct sequencing in 20 patients with both LHDL/HTG and diagnosed CHD. 10729390 2000
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 GeneticVariation disease BEFREE Hyperlipidemia is a risk factor of arteriosclerosis, stroke, and other coronary heart disease, which has been shown to correlate with single nucleotide polymorphisms of genes essential for lipid metabolism, such as lipoprotein lipase (LPL) and apolipoprotein A5 (APOA5). 29425239 2018
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.400 Biomarker disease BEFREE The role of plasma lipoprotein lipase, hepatic lipase and GPIHBP1 in the metabolism of remnant lipoproteins and small dense LDL in patients with coronary artery disease. 29174344 2018