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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
Metabolic Syndrome X
|
0.400 |
GeneticVariation
|
disease |
GWASCAT |
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.
|
21386085 |
2011 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |
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 |