CCK, cholecystokinin, 885

N. diseases: 326; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE A group of peptide-based, long-acting, stable, highly selective cholecystokinin 1 receptor (CCK-1R) agonists with the potential to treat obesity has been identified and characterized, based on systematic investigation of synthetic CCK-8 analogues with N-terminal linkage to fatty acids. 30624060 2019
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE The satiety effects and metabolic actions of cholecystokinin (CCK) have been recognized as potential therapeutic targets in obesity for decades. 30843875 2019
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE Reduced ability of cholecystokinin (CCK) to induce satiation contributes to hyperphagia and weight gain in high-fat/high-sucrose (HF/HS) diet-induced obesity, and has been linked to altered gut microbiota. 30069617 2019
CUI: C0028754
Disease: Obesity
Obesity
0.100 AlteredExpression disease BEFREE The theoretical case has been made for the development of a positive allosteric modulator (PAM) of the type 1 cholecystokinin receptor (CCK1R) having minimal intrinsic agonist activity to enhance meal-induced satiety for the treatment of obesity, while reducing the risk of side effects and/or toxicity. 30591538 2019
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE This paper describes the early history of Gastric Inhibitory Polypeptide, better referred to simply as GIP, from its isolation by purification from a crude preparation of CCK-PZ (cholecystokinin/pancreozymin) to its recognition as a key player in the pathogenesis of obesity and other metabolic disorders far removed from the enterogastrone properties by which it was originally identified. 31539554 2019
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE This review focuses on the recent and ongoing developments of CCK in the context of new therapies for obesity and type 2 diabetes. 29412823 2018
CUI: C0028754
Disease: Obesity
Obesity
0.100 AlteredExpression disease BEFREE On the other hand, TTI treatment decreased CCK-1R gene expression in obese animals compared with the obese group with no treatment (p = 0.027). 30537704 2018
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE CCK-8S (1.8 or 5.2 nmol/kg) did not alter food intake and meal pattern in DIO rats. 28724546 2017
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE Reduced CCK sensitivity best correlated with elevated serum triglycerides in normal-weight participants and with low HDL concentrations and elevated glycated hemoglobin in obese and diabetic patients.<b>Conclusions:</b> CCK responsiveness varies widely across the population, with reduced signaling in patients with obesity and diabetes. 28592602 2017
CUI: C0028754
Disease: Obesity
Obesity
0.100 PosttranslationalModification disease BEFREE We also show that CREB directly targets the Cck promoter in islets from obese (Leptin(ob/ob)) mice. 25984632 2015
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE Positive correlations were observed between TPH1, CCK, PYY, and nesfatin1 in nonobese and GOAT, ghrelin, TPH1, SERT, CCK, and PYY in humans with obesity (all P < 0.01). 26381270 2015
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE These studies underscore the potential of (pGlu-Gln)-CCK-8 for the treatment of obesity-diabetes and suggest modulation of NPY and melanocortin related pathways may be involved in the observed beneficial effects. 23315994 2013
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker disease BEFREE This Commentary provides a context for the use of efficacy pipeline pharmacogenetics (PGx) in therapeutic programs.Jordan et al. published the results of an obesity trial with a cholecystokinin-A (CCK-A) receptor agonist and concluded that CCK-A by itself does not have a central role in long-term energy balance. 19295535 2009
CUI: C0028754
Disease: Obesity
Obesity
0.100 GeneticVariation disease BEFREE Although CCK-1R polymorphisms with amino acid changes such as 21Gly to Arg, 71 Arg to Gly, and 364 Val to Ile were discovered in subjects with obesity and diabetes mellitus, these changes occur sporadically. 17584142 2007
CUI: C0028754
Disease: Obesity
Obesity
0.100 GeneticVariation disease BEFREE In addition, beta3 adrenergic receptor gene polymorphism (Try64Arg) and cholecystokinin (CCK)-A receptor (R) gene polymorphism (-81A/G, -128G/T), which are both associated with obesity, were investigated. 16362631 2006
CUI: C0028754
Disease: Obesity
Obesity
0.100 GeneticVariation disease BEFREE Polymorphism or mutations in the CCK receptors may be involved in type 2 diabetes mellitus and obesity. 11773861 2002
CUI: C0028754
Disease: Obesity
Obesity
0.100 GeneticVariation disease BEFREE The integrity of the cholecystokinin receptor gene in gallbladder disease and obesity. 7489984 1995
CUI: C0028754
Disease: Obesity
Obesity
0.100 GeneticVariation disease BEFREE Abnormal processing of the human cholecystokinin receptor gene in association with gallstones and obesity. 7557108 1995