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: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE Mutations in the lipoprotein lipase gene causing decreased lipoprotein lipase activity are associated with surrogate markers of insulin resistance and the metabolic syndrome in humans. 28502509 2018
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE This presumed impaired effect of insulin on LPL postprandially could be an important contributor to the atherogenic dyslipidaemia described in insulin resistance syndrome. 11895454 2002
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE Finally, we replicated the LPL and CETP loci previously found to be associated with MetS in Europeans. 26507551 2015
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease GWASCAT Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. 22399527 2012
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE This was the first study this kind to show an association between LPL and large VLDL particle size within the MetS, a pattern associated with higher IR. 21854610 2011
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE Increased risk of developing metabolic syndrome (MetS) has been associated with the APOA5, APOC1, BRAP, BUD13, CETP, LIPA, LPL, PLCG1, and ZPR1 genes. 27827461 2016
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE A novel African American-specific variant, rs12721054/APOC1, and rs10096633/LPL are associated with ≥3 MetS components. 25023634 2014
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE The apolipoprotein A5 Q139X, lipoprotein lipase (LPL) Hinf I, human paraoxonase 1 (PON1) 192Arg/Gln, cholesteryl ester transfer protein (CETP) Taq1B, adiponectin 45T>G and leptin (LEP) 25CAG were genotyped by real-time polymerase chain reaction in participants with and without MetS. 30381540 2018
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 AlteredExpression disease BEFREE These results show that decreased expression of LPL possibly causes the insulin resistance, in addition to hypertriglyceridemia, in metabolic syndrome. 16941273 2006
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE Lipoprotein lipase (LPL) hydrolyzes triglycerides in lipoprotein to supply fatty acids, and its deficiency leads to hypertriglyceridemia, thereby inducing metabolic syndrome (MetSyn). 31234537 2019
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease GWASCAT A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. 21386085 2011
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE The S447X variant of lipoprotein lipase gene is associated with metabolic syndrome and lipid levels among Turks. 17555736 2007
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 AlteredExpression disease BEFREE This appears to be the first reported genetic association with the insulin-resistance syndrome and may reflect genotype specific differences in the regulation of lipoprotein lipase by insulin. 7905375 1993
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 PosttranslationalModification disease BEFREE The aim of this study was to analyze the level of DNA methylation of several lipoprotein lipase (LPL)-promoter-CpG dinucleotides in a CpG island region and relate this to the gene and protein expression levels in human visceral adipose tissue (VAT) from individuals with and without MetS. 29046332 2018
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE Logistic regression analysis after adjustment for age, sex, adiponectin and S447X polymorphism demonstrated that LPL mass was inversely associated with CHD in men and both genders (p=0.02), with hypertension confined to women (p=0.04) and with MS likelihood in both genders combined and women [odds ratio 1.51 (95% CI 1.14-2.00) for halving the likelihood]. 19191728 2009
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE In conclusion, our results show the involvement of the variants of ESR1, LPL and CETP genes in metabolic events related to MetS or some of its features. 26370976 2015
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Therapeutic disease RGD Gly in MS rats decreased body weight, intra-abdominal adipose tissue, adipocyte hypertrophy, blood pressure, triglycerides, insulin, HOMA-IR index, leptin, total fatty acids, non-esterified fatty acids and LPL activity. 26996629 2016
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE This study shows that carrier status of one defective lipoprotein-lipase allele is associated with impaired insulin sensitivity, an atherogenic lipoprotein profile and other characteristics of the metabolic syndrome, which are risk factors for atherosclerotic vascular disease. 11914743 2002
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE LPL may influence atherosclerosis risk through pleiotropic effects on each aspect of the metabolic syndrome. 16755277 2007
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE This haplotype-based genetic analysis provides compelling evidence that variation in the LPL gene plays a role in determining insulin resistance in this ethnic group with a high prevalence of the insulin resistance syndrome. 14693718 2004
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 AlteredExpression disease BEFREE The fourth most common haplotype based on 19 SNPs (haplotype 19-4) was associated with increased LPL activity as well as multiple phenotypes related to the metabolic syndrome. 15928243 2005
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 AlteredExpression disease BEFREE Significant increases were observed in blood pressure, HOMA-IR, leptin, triglycerides, insulin, intra-abdominal fat, and number of fat cells per field (<i>p</i> = 0.001) and in advanced glycosylation products, adipocyte area, LPL, HSL activities and/or expression (<i>p</i> ≤ 0.01) in the MS groups progressively from the third month onward. 31284400 2019
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE LPL mass was significantly lower in patients with PvuII and HindIII mutant alleles (P2 and H2) and decreased as the number of MetSyn components increased in all PvuII and HindIII haplotypes. 23927945 2013
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 GeneticVariation disease BEFREE This study investigated the relationship between two common LPL variants and the presence of MetS and its individual components. 27676127 2016
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.400 Biomarker disease BEFREE A 3-SNP GRS and MetRS were generated in the EPIC-Norfolk cohort (n = 20,074) based on 3 SNPs in LPL and APOA5 or the number of Metabolic Syndrome criteria present (maximum 5), respectively. 30910668 2020