Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE Fasting plasma leptin, triglycerides, cholesterol and phospholipids are elevated, suggesting metabolic syndrome. 29206867

2017

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker MGD Dysregulation of the Hypothalamus-Pituitary-Adrenal Axis in Male and Female, Genetically Obese (ob/ob) Mice. 21554665

1992

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE Notably, L/A outperformed individual leptin or adiponectin in discriminating a diagnosis of MS (all P < 0.02 in AUC comparisons). 29020116

2017

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE Phase 1.Body mass index (BMI), waist circumference, serum glucose, HbA1C, lipids, leptin, cortisol, insulin resistance index (HOMA-IR), metabolic syndrome and the frequencies of SNPs were assessed in 56 CLZ-treated patients (78.6% males).Phase 2. 20591628

2010

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE We demonstrated previously that offspring born to pregnant mice lacking the endothelial nitric oxide synthase (eNOS+/-) gene have hypertension (HTN) as adults and, when fed a high-fat diet (HFD), develop a metabolic syndrome (MS) phenotype. 30521799

2019

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 AlteredExpression BEFREE Hormone replacement therapy increases eNOS activity and normalizes some characteristics of metabolic syndrome. 28196859

2017

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE Leptin promotes adequate caloric intake and glycemia in healthy lean individuals, harnessing the benefits of the ideal therapy against metabolic syndrome. 30792083

2019

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 AlteredExpression BEFREE A Receiver Operator Characteristic curve was used to identify the ability of adiponectin and leptin level to predict the MetS. 31341853

2019

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 AlteredExpression BEFREE The adipokines DPP-4 and leptin in the serum can influence the body fat distribution of patients with T2MD; there is an important association of DPP-4, leptin and ADPN levels with MS, which may be used as therapeutic targets for multiple metabolism disorders of T2MD. 29205013

2019

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 AlteredExpression BEFREE Patients with MetS had higher levels of leptin (14 ± 12.4) compared with those without MetS (11.2 ± 9.3 vs. 7 ± 7.1 obese and normal weight without MetS, respectively; p = .002). 27550773

2017

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 GeneticVariation BEFREE In this work we investigated the following: i) whether CAV1 is a quantitative trait locus of clustering of atherothrombotic traits associated with MS; ii) whether CVA1 is associated with hypertension or MS in hypertensive patients; and iii) whether genetic interaction between NOS3 and CAV1 is involved in the susceptibility or protection to hypertension associated with MS. To carry out the study, we genotyped 285 randomly selected individuals and 175 hypertensive patients, all of them < or = 60 years old, with two polymorphisms of the CAV1 gene: the 22285 C>T and the 22375-22375 del AC (GenBank AF125348), and the 1132T>C polymorphism of the NOS3 gene. 16601841

2006

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker CTD_human Dietary inorganic nitrate reverses features of metabolic syndrome in endothelial nitric oxide synthase-deficient mice. 20876122

2010

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE A concentration of leptin > 52.18 pg/ml (AUC = 0.81, <i>p</i> < 0.0001) and resistin > 4419.27 ng/ml (AUC = 0.67, <i>p</i> = 0.049) had a good predictive value for improvement of the LVEF in the patients without MeS. 28721146

2017

Entrez Id: 3606
Gene Symbol: IL18
IL18
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 AlteredExpression BEFREE Multivariate analysis revealed fasting plasma glucose to be the only MetS component being independently associated with expression of IL-18 in AT (p < 0.05). 21842238

2011

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE Disturbances in leptin and insulin signaling pathways are related to obesity and metabolic syndrome (MS) with increased risk of diabetes and cardiovascular disease. 22185674

2011

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE At baseline, MS was observed in 24 patients, significantly associated with insulin resistance and leptin on multivariate analysis. 30054704

2018

Entrez Id: 23411
Gene Symbol: SIRT1
SIRT1
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE These findings suggest that SIRT1 might be a new therapeutic target for the prevention of disease related to insulin resistance, such as metabolic syndrome and diabetes mellitus, although direct evidence from clinical studies in humans is needed to prove this possibility. 19455179

2009

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker CTD_human We wondered, whether eNOS deficiency in mice is associated with a phenotype mimicking the human metabolic syndrome. 12947532

2003

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 AlteredExpression BEFREE Low vitamin D level was associated with metabolic syndrome and high leptin level in subjects with nonalcoholic fatty liver disease: a community-based study. 31311491

2019

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 GeneticVariation BEFREE We studied the association of G2548A of the LEP gene and Q223R of LEPR gene polymorphisms with obesity and metabolic syndrome (MetS). 22734460

2012

Entrez Id: 23411
Gene Symbol: SIRT1
SIRT1
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE The NAD<sup>+</sup>-dependent deacetylase SIRT1, which is associated with the improvement of metabolic syndromes, such as type 2 diabetes, is a well-known longevity-related gene. 29402742

2018

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker MGD Leptin stimulates ischemia-induced retinal neovascularization: possible role of vascular endothelial growth factor expressed in retinal endothelial cells. 15331557

2004

Entrez Id: 4846
Gene Symbol: NOS3
NOS3
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker RGD Vascular endothelial function masks increased sympathetic vasopressor activity in rats with metabolic syndrome. 29127233

2018

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker MGD Leptin inhibits bone formation through a hypothalamic relay: a central control of bone mass. 10660043

2000

Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.600 Biomarker BEFREE The addition of leptin and adiponectin to the regression models did not substantially change the impact of thyroid hormones on components of MS. Our data suggest that, even within the euthyroid range, excess of truncal adipose tissue is associated with variations in FT4. 31151171

2019