A phenome-wide comparative analysis of genetic discordance between obesity and type 2 diabetes.
Daniel E CoralJuan Fernandez-TajesNeli TsereteliHugo Pomares-MillanHugo FitipaldiPascal M MutieNaemieh Atabaki-PasdarSebastian KalamajskiAlaitz PovedaTyne W Miller-FlemingXue ZhongGiuseppe N GiordanoEwan R PearsonNancy J CoxPaul W FranksPublished in: Nature metabolism (2023)
Obesity and type 2 diabetes are causally related, yet there is considerable heterogeneity in the consequences of both conditions and the mechanisms of action are poorly defined. Here we show a genetic-driven approach defining two obesity profiles that convey highly concordant and discordant diabetogenic effects. We annotate and then compare association signals for these profiles across clinical and molecular phenotypic layers. Key differences are identified in a wide range of traits, including cardiovascular mortality, fat distribution, liver metabolism, blood pressure, specific lipid fractions and blood levels of proteins involved in extracellular matrix remodelling. We find marginal differences in abundance of Bacteroidetes and Firmicutes bacteria in the gut. Instrumental analyses reveal prominent causal roles for waist-to-hip ratio, blood pressure and cholesterol content of high-density lipoprotein particles in the development of diabetes in obesity. We prioritize 17 genes from the discordant signature that convey protection against type 2 diabetes in obesity, which may represent logical targets for precision medicine approaches.
Keyphrases
- type diabetes
- insulin resistance
- glycemic control
- metabolic syndrome
- weight loss
- blood pressure
- genome wide
- high fat diet induced
- extracellular matrix
- weight gain
- cardiovascular disease
- high density
- adipose tissue
- heart rate
- body mass index
- blood glucose
- gene expression
- low density lipoprotein
- hypertensive patients
- cardiovascular events
- single cell
- fatty acid
- coronary artery disease
- microbial community
- body weight