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    Approaching the shared biology of obesity and depression: The stress axis as the locus of gene-environment interactions.
        
        Mol. Psychiatry 11, 892-902 (2006)
    
    
    
				Obesity and depression are serious public health problems and also constitute cardiovascular disease risk factors. Research organizations have called for efforts to explore the interrelationship between obesity and depression. A useful starting point is the fact that in both disorders there is dysregulation of stress systems. We review molecular and clinical evidence indicating that the mediators of the stress response are a key locus for gene-environment interactions in the shared biology of depression and obesity. Scientific milestones include translational paradigms such as mice knockouts, imaging and pharmacogenomic approaches that can identify new therapeutic strategies for those burdened by these two afflictions of contemporary civilization. Perspectives for the future are promising. Our ability to dissect the underpinnings of common and complex diseases with shared substrates will be greatly enhanced by the Genes and Environment Initiative, the emerging Large Scale Studies of Genes and Environment in Common Disease, and the UK Biobank Project.
			
			
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
     
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2006
    
 
     
    
        HGF-Berichtsjahr
        0
    
 
    
    
        ISSN (print) / ISBN
        1359-4184
    
 
    
        e-ISSN
        1476-5578
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Molecular Psychiatry
    
 
		
    
        Quellenangaben
        
	    Band: 11,  
	    Heft: 10,  
	    Seiten: 892-902 
	    
	    
	
    
 
  
         
        
            Verlag
            Nature Publishing Group
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
    
        Institut(e)
        Institute of Pancreatic Islet Research (IPI)
    
 
     
     
     
     
     	
    
        PubMed ID
        16880826
    
    
    
        Erfassungsdatum
        2006-12-31