Assessing risk prediction models using individual participant data from multiple studies.
    
    
        
    
    
        
        Am. J. Epidemiol. 179, 621-632 (2014)
    
    
    
      
      
	
	    Individual participant time-to-event data from multiple prospective epidemiologic studies enable detailed investigation into the predictive ability of risk models. Here we address the challenges in appropriately combining such information across studies. Methods are exemplified by analyses of log C-reactive protein and conventional risk factors for coronary heart disease in the Emerging Risk Factors Collaboration, a collation of individual data from multiple prospective studies with an average follow-up duration of 9.8 years (dates varied). We derive risk prediction models using Cox proportional hazards regression analysis stratified by study and obtain estimates of risk discrimination, Harrell's concordance index, and Royston's discrimination measure within each study; we then combine the estimates across studies using a weighted meta-analysis. Various weighting approaches are compared and lead us to recommend using the number of events in each study. We also discuss the calculation of measures of reclassification for multiple studies. We further show that comparison of differences in predictive ability across subgroups should be based only on within-study information and that combining measures of risk discrimination from case-control studies and prospective studies is problematic. The concordance index and discrimination measure gave qualitatively similar results throughout. While the concordance index was very heterogeneous between studies, principally because of differing age ranges, the increments in the concordance index from adding log C-reactive protein to conventional risk factors were more homogeneous.
	
	
	    
	
       
      
	
	    
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        Publication type
        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
    
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        Keywords
        C index; D measure; coronary heart disease; individual participant data; inverse variance; meta-analysis; risk prediction; weighting; Cardiovascular-disease Prediction; To-event Analysis; Time-scale; Regression-models; Cancer; Metaanalysis; Choice; Ability; Cohort; Blood
    
 
    
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        Language
        english
    
 
    
        Publication Year
        2014
    
 
    
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        HGF-reported in Year
        2014
    
 
    
    
        ISSN (print) / ISBN
        0002-9262
    
 
    
        e-ISSN
        1476-6256
    
 
    
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	    Volume: 179,  
	    Issue: 5,  
	    Pages: 621-632 
	    Article Number: ,  
	    Supplement: ,  
	
    
 
    
        
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            Oxford University Press
        
 
        
            Publishing Place
            Cary
        
 
	
        
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        Reviewing status
        Peer reviewed
    
 
    
        Institute(s)
        Institute of Epidemiology (EPI)
    
 
    
        POF-Topic(s)
        30202 - Environmental Health
    
 
    
        Research field(s)
        Genetics and Epidemiology
    
 
    
        PSP Element(s)
        G-504000-006
    
 
    
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        Erfassungsdatum
        2014-01-27