PPARGC1A, PPARG coactivator 1 alpha, 10891

N. diseases: 350; N. variants: 42
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE A difference between obese and nonobese subjects in polymorphism PPARGC1A distribution was observed. 26185753 2015
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE This study aims to test whether 10 polymorphisms in obesity-related genes methionine sulfoxide reductase A (MSRA), transcription factor AP-2 beta (TFAP2B), melanocortin 4 receptor (MC4R), neurexin 3 (NRXN3), peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PPARGC1A), transmembrane protein 18 (TMEM18), homolog of S. cerevisiae Sec16 (SEC16B), homeobox B5 (HOXB5) and olfactomedin 4 (OLFM4) are associated with the risk of obesity in Portuguese children. 24670271 2014
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE Increased risk of obesity associated with the variant allele of the PPARGC1A Gly482Ser polymorphism in physically inactive elderly men. 16474966 2006
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE We tested whether a targeted reduction in hepatic peroxisome proliferator-activated receptor γ coactivator-1α (PGC-1α), which has been shown to occur with obesity, had a negative impact on the metabolic effects of FGF21. 29215172 2018
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE The Gly482Ser polymorphism in peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PPARGC1A) has been demonstrated to be associated with diabetes, obesity and hypertension, all of which are important risk factors for left ventricular diastolic dysfunction. 19077249 2008
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE The aim of this study was to clarify whether common single nucleotide polymorphisms (SNPs) of the Peroxisome Proliferator-Activated Receptor-γ (PPAR-γ) gene (rs1801282) and the Peroxisome Proliferator-Activated Receptor-γ Coactivator-1 (PGC-1α) gene (rs8192673) are associated with obesity indexes (BMI, waist circumference) in subjects with type 2 diabetes mellitus (T2DM) in Caucasian population. 25928419 2015
CUI: C0028754
Disease: Obesity
Obesity
0.300 GeneticVariation disease BEFREE A single nucleotide variant of the PPARGC1A gene (rs8192678) is associated with T2D susceptibility, relative risk of obesity and insulin resistance, and lower indices of β cell function. 29186342 2018
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE New wine into old wineskins: PGC-1α and NF-κB in obesity and acute pancreatitis. 30570131 2019
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE Recent studies report that PGC-1α-null mice develop late-onset obesity and that the neuronal inactivation of PGC-1α causes increased food intake. 22016516 2011
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE Furthermore, the transcript and protein levels of transcriptional coactivator peroxisome proliferator-activated receptor γ (PPARγ) coactivator 1α (PGC-1α) and estrogen-related receptor-α (ERRα) in DIO-R mice were significantly up-regulated compared with the DIO mice. 28444662 2017
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE We confirm the role of PPARGC1A in muscle and show some support for inflammation in adipose from European American subjects but find prominent roles for lipid metabolism in insulin sensitivity independent of obesity in both tissues. 21266331 2011
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE The peroxisome proliferator-activated receptor gamma (PPARgamma) and PPARgamma coactivator-1alpha (PGC-1alpha) system plays an important role in the regulation of efficient energy utilization and oxidative phosphorylation, both of which are decreased in obesity and insulin resistance. 19966034 2010
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease RGD Sex differences in the effect of high-fat diet feeding on rat white adipose tissue mitochondrial function and insulin sensitivity. 22401878 2012
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE Two strong positional candidates, the human peroxisome proliferator-activated receptor gamma coactivator 1 (PPARGC1) and cholecystokinin A receptor (CCKAR) with major roles in the development of obesity, are located in this region. 14740316 2004
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE In this review, we outline the function of PGC-1 coactivators in physiological and pathological conditions as well as the complex interplay of metabolic dysregulation and inflammation in obesity with special focus on skeletal muscle. 24258516 2014
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE The aim of the present study was to determine the possible association of five single-nucleotide polymorphisms (SNPs) located in the IGF2, LEPR, POMC, PPARG, and PPARGC1 genes with obesity or obesity-related risk phenotypes. 25923461 2015
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE PGC-1α has been implicated in the pathogenic conditions including obesity, type 2 diabetes, neurodegeneration, and cardiomyopathy, whereas PGC-1β plays an important role in plasma lipoprotein homeostasis and serves as a hepatic target for niacin, a potent hypotriglyceridemic drug. 21325336 2011
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE Special emphasis is placed on the effects of high fat diet (HFD) feeding on expression of nuclear-encoded mitochondrial genes (NEMGs) nuclear receptor factor 1 (NRF-1) and 2 (NRF-2) and peroxisome proliferator receptor gamma coactivator 1 alpha (PGC-1α) in the onset and progression of insulin resistance during obesity and how HFD-induced alterations in NEMG expression affect skeletal muscle mitochondrial adaptations in relation to beta oxidation of fatty acids. 28420087 2017
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE These studies suggest functional differences of PPARGC1 haplotypes in human energy metabolism and support a role of PPARGC1 in obesity. 11916956 2002
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE The current study is the first to provide evidence that Met could ameliorate muscle atrophy in high-fat diet induced obesity and this effect may be in part due to regulation of PGC-1α-FoxO3 pathway. 30320911 2019
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE Although primarily investigated for its therapeutic potential in obesity and skeletal muscle differentiation, the ability of PGC-1α to alter a multitude of cellular functions has sparked interest in its role in the vasculature. 27312223 2016
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE An interaction between ERRα and peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α) has also recently been shown to regulate an enzyme in the β-oxidation of free fatty acids, thereby suggesting that ERRα plays an important role in obesity and type 2 diabetes. 29216352 2018
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE We examined the expression of candidate genes involved in adipocyte proliferation and/or differentiation [CCAAT/enhancer-binding protein (C/EBP) alpha, C/EBPdelta, GATA domain-binding protein 3 (GATA3), C/EBPbeta, peroxisome proliferator-activated receptor (PPAR) gamma2, signal transducer and activator of transcription 5A (STAT5A), Wnt-10b, tumor necrosis factor alpha, sterol regulatory element-binding protein 1c (SREBP1c), 11 beta-hydroxysteroid dehydrogenase, PPARG angiopoietin-related protein (PGAR), insulin-like growth factor 1, PPARgamma coactivator 1alpha, PPARgamma coactivator 1beta, and PPARdelta] in subcutaneous adipose tissue from 42 obese individuals with type 2 diabetes and 25 non-diabetic subjects matched for age and obesity. 17030965 2006
CUI: C0028754
Disease: Obesity
Obesity
0.300 Biomarker disease BEFREE Studies in mice have shown that increased PGC-1α expression may be beneficial or deleterious, depending on the tissue: in adipose tissue, it promotes thermogenesis and thus protects against energy overload, such as seen in diabetes and obesity; in muscle, PGC-1α induces a change of phenotype towards oxidative metabolism. 25753246 2015
CUI: C0028754
Disease: Obesity
Obesity
0.300 Therapeutic disease RGD Supplementing obese Zucker rats with niacin induces the transition of glycolytic to oxidative skeletal muscle fibers. 23256146 2013