Construction of confidence regions in the ROC space after the estimation of the optimal Youden index‐based cut‐off point
After establishing the utility of a continuous diagnostic marker investigators will typically address the question of determining a cut‐off point which will be used for diagnostic purposes in clinical decision making. The most commonly used optimality criterion for cut‐off point selection in the con...
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Published in | Biometrics Vol. 70; no. 1; pp. 212 - 223 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishers
01.03.2014
Blackwell Publishing Ltd International Biometric Society |
Subjects | |
Online Access | Get full text |
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Summary: | After establishing the utility of a continuous diagnostic marker investigators will typically address the question of determining a cut‐off point which will be used for diagnostic purposes in clinical decision making. The most commonly used optimality criterion for cut‐off point selection in the context of ROC curve analysis is the maximum of the Youden index. The pair of sensitivity and specificity proportions that correspond to the Youden index‐based cut‐off point characterize the performance of the diagnostic marker. Confidence intervals for sensitivity and specificity are routinely estimated based on the assumption that sensitivity and specificity are independent binomial proportions as they arise from the independent populations of diseased and healthy subjects, respectively. The Youden index‐based cut‐off point is estimated from the data and as such the resulting sensitivity and specificity proportions are in fact correlated. This correlation needs to be taken into account in order to calculate confidence intervals that result in the anticipated coverage. In this article we study parametric and non‐parametric approaches for the construction of confidence intervals for the pair of sensitivity and specificity proportions that correspond to the Youden index‐based optimal cut‐off point. These approaches result in the anticipated coverage under different scenarios for the distributions of the healthy and diseased subjects. We find that a parametric approach based on a Box–Cox transformation to normality often works well. For biomarkers following more complex distributions a non‐parametric procedure using logspline density estimation can be used. |
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Bibliography: | http://dx.doi.org/10.1111/biom.12107 ark:/67375/WNG-3B8DKS4R-B istex:5A68757DDF125053C05F6215B7AE0A14DE6B4BFA ArticleID:BIOM12107 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0006-341X 1541-0420 1541-0420 |
DOI: | 10.1111/biom.12107 |