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    The metabolic burden of sleep loss.
        
        Lancet Diabet. Endocrinol. 3, 52-62 (2015)
    
    
    
				In parallel with the increasing prevalence of obesity and type 2 diabetes, sleep loss has become common in modern societies. An increasing number of epidemiological studies show an association between short sleep duration, sleep disturbances, and circadian desynchronisation of sleep with adverse metabolic traits, in particular obesity and type 2 diabetes. Furthermore, experimental studies point to distinct mechanisms by which insufficient sleep adversely affects metabolic health. Changes in the activity of neuroendocrine systems seem to be major mediators of the detrimental metabolic effects of insufficient sleep, through favouring neurobehavioural outcomes such as increased appetite, enhanced sensitivity to food stimuli, and, ultimately, a surplus in energy intake. The effect of curtailed sleep on physical activity and energy expenditure is less clear, but changes are unlikely to outweigh increases in food intake. Although long-term interventional studies proving a cause and effect association are still scarce, sleep loss seems to be an appealing target for the prevention, and probably treatment, of metabolic disease.
			
			
		Impact Factor
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Times Cited
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					Cited By
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
     
    
    
        Schlagwörter
        Slow-wave Sleep; Eye-movement Sleep; Body-mass Index; Energy-expenditure; Food-intake; Insufficient Sleep; Healthy-men; Leptin Levels; Weight-gain; Insulin Sensitivity
    
 
     
    
    
        Sprache
        englisch
    
 
    
        Veröffentlichungsjahr
        2015
    
 
    
        Prepublished im Jahr 
        2014
    
 
    
        HGF-Berichtsjahr
        2014
    
 
    
    
        ISSN (print) / ISBN
        2213-8587
    
 
    
        e-ISSN
        2213-8595
    
 
     
     
     
	     
	 
	 
    
        Zeitschrift
        Lancet Diabetes and Endocrinology
    
 
		
    
        Quellenangaben
        
	    Band: 3,  
	    Heft: 1,  
	    Seiten: 52-62 
	    
	    
	
    
 
  
         
        
            Verlag
            Elsevier
        
 
        
            Verlagsort
            New York
        
 
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Begutachtungsstatus
        Peer reviewed
    
 
     
    
        POF Topic(s)
        90000 - German Center for Diabetes Research
    
 
    
        Forschungsfeld(er)
        Helmholtz Diabetes Center
    
 
    
        PSP-Element(e)
        G-502400-003
    
 
     
     	
    
        PubMed ID
        24731536
    
    
    
        WOS ID
        WOS:000353030400025
    
    
        Erfassungsdatum
        2014-04-09