Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE PPARα agonists (fibrates) and PPARγ agonists (thiazolidinediones) are used for the treatment of hypertriglyceridemia and type 2 diabetes, respectively. 31825687 2020
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE Pemafibrate is the first clinically-available selective peroxisome proliferator-activated receptor α modulator (SPPARMα) that has been shown to effectively improve hypertriglyceridemia and low high-density lipoprotein cholesterol (HDL-C) levels. 31766193 2019
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE Rosa rugosa flavonoids exhibited PPARα agonist-like effects on genetic severe hypertriglyceridemia of mice. 31100436 2019
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE Fenofibrate, a peroxisome proliferator-activated receptor-α (PPARα) agonist, is used to treat patients with hypercholesterolemia and hypertriglyceridemia in order to reduce the risk of development of the atherosclerotic cardiovascular disease. 31237119 2019
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 AlteredExpression phenotype BEFREE Fenofibrate, a third-generation fibric acid derivative, is an activator of PPARα indicated for the treatment of mixed dyslipidemia and hypertriglyceridemia in adults. 30970278 2019
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 GeneticVariation phenotype BEFREE The results obtained in the codominant and overdominant models for the <i>PPAR-y</i> polymorphism showed a tendency to statistical significance (the C/G genotype inclined to hypertriglyceridemia), and were statistically significant in the codominant, dominant, and recessive models (the C/C genotype predisposed to increased blood pressure). 29315078 2018
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE Gemfibrozil, a peroxisome proliferator-activated receptor α (PPARα) agonist, is widely used for hypertriglyceridaemia and mixed hyperlipidaemia. 28374976 2017
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 AlteredExpression phenotype BEFREE In relation to its effects on the hyperglycemia and hypertriglyceridemia, few is known about the mechanisms in which this compound may be acting, therefore, the aim of the present study was to determine if CGA acts as an insulin secretagogue increasing intracellular calcium concentrations ([Ca<sup>2+</sup>]<sub>i</sub>) in RINm5F cells; or as an insulin sensitizer and lipid-lowering agent stimulating the expression of PPARγ and PPARα, respectively, in 3T3-L1 adipocytes. 28759754 2017
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE Treatment of hypertriglyceridaemia is based on fibrates, which activate the peroxisome proliferator-activated receptor alpha (PPARα). 28251701 2017
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 GeneticVariation phenotype BEFREE PPAR-α Agonist Fenofibrate Reduces Insulin Resistance in Impaired Glucose Tolerance Patients with Hypertriglyceridemia: A Cross-Sectional Study. 28361462 2017
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 AlteredExpression phenotype BEFREE Periostin promotes liver steatosis and hypertriglyceridemia through downregulation of PPARα. 25003192 2014
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE Fenofibrate, a peroxisome proliferator-activated receptor alpha (PPAR-α) agonist, has been used for decades to treat hypertriglyceridaemia and mixed dyslipidaemia. 24529079 2014
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 GeneticVariation phenotype BEFREE This study examined the main effects of both single-locus and multilocus interactions among genetic variants in Chinese Han individuals to test the hypothesis that PPAR-α/δ/γ polymorphisms may contribute to the etiology of hypertriglyceridemia independently and/or through such complex interactions. 23262340 2013
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 GeneticVariation phenotype BEFREE Differential regulation of the human versus the mouse apolipoprotein AV gene by PPARalpha. Implications for the study of pharmaceutical modifiers of hypertriglyceridemia in mice. 19362162 2009
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype BEFREE One potential advantage in studying PPARalpha agonists is that they have been very well tolerated when used in humans to treat conditions such as elevated triglycerides. 16484546 2006
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 Biomarker phenotype CTD_human Association between the PPARalpha-L162V polymorphism and components of the metabolic syndrome. 15309680 2004
CUI: C0020557
Disease: Hypertriglyceridemia
Hypertriglyceridemia
0.400 GeneticVariation phenotype BEFREE We assessed, in the Quebec City population, the allele frequency and haplotype distributions of mutations in genes related to HTG, such as the apolipoprotein E (APOE) (C112R and C158R), the apolipoprotein CIII (APOC3) (C-482T and C3238G) and the peroxisome proliferator-activated receptor alpha (PPARalpha) (L162V) genes. 15549499 2004