Gräßler, J.* ; Kopprasch, S.* ; Passauer, J.* ; Fischer, S.* ; Schuhmann, K.* ; Bergmann, S.* ; Siegert, G.* ; Shevchenko, A.* ; Bornstein, S.R.* ; Julius, U.*
    
 
    
        
Differential effects of lipoprotein apheresis by lipidfiltration or dextran sulfate adsorption on lipidomic profile.
    
    
        
    
    
        
        Atherosclerosis 14, 151-155 (2013)
    
    
		
		
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			Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
		
     
    
		
		
			
				OBJECTIVE AND METHODS: Acute modification of plasma lipidomic profile was assessed by top-down shotgun profiling on a LTQ Orbitrap hybrid mass spectrometer in 14 patients treated with two different apheresis techniques: plasma lipidfiltration (LF) and whole blood dextran sulfate adsorption (DSA). RESULTS: Patients treated with DSA revealed a significantly more pronounced reduction of LDL-cholesterol (LDL-C), a diminished decrease of HDL-cholesterol (HDL-C) and triglycerides (TG), and a similar reduction in lipoprotein (a) (Lp(a)) level. Against the overall tendency of reduction of lipid metabolites of all lipid classes in post-apheresis plasma, independent of apheresis technology applied, a highly significant increase of phosphatidylethanolamines (PE) in response to DSA was observed. CONCLUSION: These data indicate that DSA technology may be associated with an activation or damage of blood cells at contact surface which subsequently leads to a massive liberation of cellular and membrane PE's. Pathophysiological consequences, especially with respect to coagulation system and oxidative stress, have to be further elucidated.
			
			
				
			
		 
		
			
				
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
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        englisch
    
 
    
        Veröffentlichungsjahr
        2013
    
 
    
        Prepublished im Jahr 
        
    
 
    
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        0
    
 
    
    
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        0021-9150
    
 
    
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        1879-1484
    
 
    
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	    Band: 14,  
	    Heft: 1,  
	    Seiten: 151-155 
	    Artikelnummer: ,  
	    Supplement: ,  
	
    
 
  
        
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            Verlag
            Elsevier
        
 
        
            Verlagsort
            Amsterdam
        
 
	
        
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        Peer reviewed
    
 
    
        Institut(e)
        Institute of Pancreatic Islet Research (IPI)
    
 
    
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        Erfassungsdatum
        2013-12-31