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    Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations.
        
        Mol. Nutr. Food Res. 51, 178-184 (2007)
    
    
    
	    The human acyl-CoA-binding protein (ACBP) is a potential candidate gene of type 2 diabetes (T2D), since it plays a central role in determining the intracellular concentration of activated fatty acids which contribute to insulin resistance. The aim of our study was to evaluate whether single nucleotide polymorphisms (SNPs) of the ACBP gene are associated with risk of T2D. Genotyping of eight SNPs (rs2084202, rs3731607, rs8192501, rs8192504, rs2244135, rs2276596, rs8192506, rs2289948) was performed in 192 incident T2D subjects and 384 matched controls of the European Prospective Investigation into Cancer and Nutrition-Potsdam cohort. A putative promoter SNP (rs2084202) of splice variant ACBP 1c showed decreased risk of T2D (odds ratio (OR) 0.63, 95% CI 0.41-0.96). The haplotype, that contained the mutant base of rs2084202 showed similar evidence for the association with disease risk as single SNP rs2084202. In a second population-based study, Cooperative Health Research in the Augsburg Region of 226 individuals with T2D and 863 control subjects a borderline significant association between rs2084202 and T2D (OR 0.72, 95% CI 0.51-1.01) was observed. In summary, we obtained evidence from two Caucasian study populations that the minor allele of ACBP rs2084202 might be associated with reduced risk of T2D.
	
	
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        Publication type
        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
     
    
    
        Keywords
        Acyl-CoA-binding protein; Association study; Haplotype; Single nucleotide polymorphism; Type 2 diabetes
    
 
     
    
    
        Language
        english
    
 
    
        Publication Year
        2007
    
 
     
    
        HGF-reported in Year
        0
    
 
    
    
        ISSN (print) / ISBN
        1613-4125
    
 
    
        e-ISSN
        1613-4133
    
 
    
     
     
	     
	 
	 
     
	
    
        Quellenangaben
        
	    Volume: 51,  
	    Issue: 2,  
	    Pages: 178-184 
	    
	    
	
    
 
    
         
        
            Publisher
            Wiley
        
 
         
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Reviewing status
        Peer reviewed
    
 
    
        Institute(s)
        Institute of Epidemiology (EPI)
    
 
    
        POF-Topic(s)
        30503 - Chronic Diseases of the Lung and Allergies
    
 
    
        Research field(s)
        Genetics and Epidemiology
    
 
    
        PSP Element(s)
        G-503900-003
    
 
     
     	
    
        PubMed ID
        17262885
    
    
    
        WOS ID
        000245098700003
    
    
        Scopus ID
        34250825208
    
    
        Erfassungsdatum
        2007-12-31