An investigation of the MC-SIMEX method with application to measurement error in periodontal outcomes
Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distin...
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Published in | Statistics in medicine Vol. 28; no. 28; pp. 3523 - 3538 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
10.12.2009
Wiley Subscription Services, Inc |
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Online Access | Get full text |
ISSN | 0277-6715 1097-0258 1097-0258 |
DOI | 10.1002/sim.3656 |
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Abstract | Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distinct measurement error characteristics. Because PPD is recorded in whole millimeters, it may be regarded as discrete and its associated error as misclassification error. This study investigates the impact of this measurement error when evaluating the effect of periodontal disease status on levels of inflammatory markers in gingival crevicular fluid (GCF). The marker readings are either left or right censored, due to quantities that are either too small to be reliably quantified or so large that they saturate the detector. Additionally, marker readings from multiple periodontal sites within a subject's mouth are correlated. These considerations give rise to a clustered survival model for the marker readings in which the discrete predictor of interest is misclassified. Associations between the GCF markers and periodontal assessments are corrected for misclassification error using the MC‐SIMEX method. Simulation studies reveal the impact of varying degrees of misclassification error on associations of interest. Analysis of pilot data from a periodontal study, for which examiner misclassification rates are estimated from calibration studies, further illustrates the approach. Copyright © 2009 John Wiley & Sons, Ltd. |
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AbstractList | Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distinct measurement error characteristics. Because PPD is recorded in whole millimeters, it may be regarded as discrete and its associated error as misclassification error. This study investigates the impact of this measurement error when evaluating the effect of periodontal disease status on levels of inflammatory markers in gingival crevicular fluid (GCF). The marker readings are either left or right censored, due to quantities that are either too small to be reliably quantified or so large that they saturate the detector. Additionally, marker readings from multiple periodontal sites within a subject's mouth are correlated. These considerations give rise to a clustered survival model for the marker readings in which the discrete predictor of interest is misclassified. Associations between the GCF markers and periodontal assessments are corrected for misclassification error using the MC-SIMEX method. Simulation studies reveal the impact of varying degrees of misclassification error on associations of interest. Analysis of pilot data from a periodontal study, for which examiner misclassification rates are estimated from calibration studies, further illustrates the approach.Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distinct measurement error characteristics. Because PPD is recorded in whole millimeters, it may be regarded as discrete and its associated error as misclassification error. This study investigates the impact of this measurement error when evaluating the effect of periodontal disease status on levels of inflammatory markers in gingival crevicular fluid (GCF). The marker readings are either left or right censored, due to quantities that are either too small to be reliably quantified or so large that they saturate the detector. Additionally, marker readings from multiple periodontal sites within a subject's mouth are correlated. These considerations give rise to a clustered survival model for the marker readings in which the discrete predictor of interest is misclassified. Associations between the GCF markers and periodontal assessments are corrected for misclassification error using the MC-SIMEX method. Simulation studies reveal the impact of varying degrees of misclassification error on associations of interest. Analysis of pilot data from a periodontal study, for which examiner misclassification rates are estimated from calibration studies, further illustrates the approach. Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distinct measurement error characteristics. Because PPD is recorded in whole millimeters, it may be regarded as discrete and its associated error as misclassification error. This study investigates the impact of this measurement error when evaluating the effect of periodontal disease status on levels of inflammatory markers in gingival crevicular fluid (GCF). The marker readings are either left or right censored, due to quantities that are either too small to be reliably quantified or so large that they saturate the detector. Additionally, marker readings from multiple periodontal sites within a subject's mouth are correlated. These considerations give rise to a clustered survival model for the marker readings in which the discrete predictor of interest is misclassified. Associations between the GCF markers and periodontal assessments are corrected for misclassification error using the MC‐SIMEX method. Simulation studies reveal the impact of varying degrees of misclassification error on associations of interest. Analysis of pilot data from a periodontal study, for which examiner misclassification rates are estimated from calibration studies, further illustrates the approach. Copyright © 2009 John Wiley & Sons, Ltd. Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distinct measurement error characteristics. Because PPD is recorded in whole millimeters, it may be regarded as discrete and its associated error as misclassification error. This study investigates the impact of this measurement error when evaluating the effect of periodontal disease status on levels of inflammatory markers in gingival crevicular fluid (GCF). The marker readings are either left or right censored, due to quantities that are either too small to be reliably quantified or so large that they saturate the detector. Additionally, marker readings from multiple periodontal sites within a subject's mouth are correlated. These considerations give rise to a clustered survival model for the marker readings in which the discrete predictor of interest is misclassified. Associations between the GCF markers and periodontal assessments are corrected for misclassification error using the MC-SIMEX method. Simulation studies reveal the impact of varying degrees of misclassification error on associations of interest. Analysis of pilot data from a periodontal study, for which examiner misclassification rates are estimated from calibration studies, further illustrates the approach. Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth of the space between a tooth and the surrounding gum. In larger studies, these assessments are made by multiple examiners, each having distinct measurement error characteristics. Because PPD is recorded in whole millimeters, it may be regarded as discrete and its associated error as misclassification error. This study investigates the impact of this measurement error when evaluating the effect of periodontal disease status on levels of inflammatory markers in gingival crevicular fluid (GCF). The marker readings are either left or right censored, due to quantities that are either too small to be reliably quantified or so large that they saturate the detector. Additionally, marker readings from multiple periodontal sites within a subject's mouth are correlated. These considerations give rise to a clustered survival model for the marker readings in which the discrete predictor of interest is misclassified. Associations between the GCF markers and periodontal assessments are corrected for misclassification error using the MC-SIMEX method. Simulation studies reveal the impact of varying degrees of misclassification error on associations of interest. Analysis of pilot data from a periodontal study, for which examiner misclassification rates are estimated from calibration studies, further illustrates the approach. [PUBLICATION ABSTRACT] |
Author | Bandyopadhyay, Dipankar Slate, Elizabeth H. |
AuthorAffiliation | Department of Biostatistics, Bioinformatics and Epidemiology Medical University of South Carolina 135 Cannon Street Charleston, SC 29425 |
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References_xml | – reference: Wang N, Lin X, Gutierrez RG, Carroll RJ. Bias analysis and simex approach in generalized linear mixed measurement error models. Journal of the American Statistical Association 1998; 93:249-261. – reference: Li Y, Lin X. Covariate measurement errors in frailty models for clustered survival data. Biometrika 2000; 87(4):849-866. DOI: 10.1093/biomet/87.4.849. – reference: Dafni UG, Tsiatis AA. Evaluating surrogate markers of clinical outcome when measured with error. Biometrics 1998; 54:1445-1462. – reference: Li Y, Lin X. Functional inference in frailty measurement error models for clustered survival data using the simex approach. Journal of the American Statistical Association 2003; 98:191-203. – reference: Fernandes JK, Salinas CF, London SD, Wiegand RE, Hill EG, Slate EH, Grewal JS, Werner P, Sanders JJ. Lopes-Virella MF. Prevalence of periodontal disease in Gullah African American diabetics. Journal of Dental Research 2006; 85(Special Issue A):0997. Available from: URL: www.dentalresearch.org. – reference: Rodbard D. Statistical estimation of the minimal detectable concentration ('sensitivity') for radioligand assays. Analytical Biochemistry 1978; 90:1-12. – reference: Tsiatis AA, DeGruttola V, Wulfsohn MS. Modeling the relationship of survival to longitudinal data measured with error. Applications to survival and CD4 counts in patients with AIDS. Journal of the American Statistical Association 1995; 90:27-37. – reference: Kowalski J, Tu XM. A generalized estimating equation approach to modelling incompatible data formats with covariate measurement error: application to human immunodeficiency virus immune markers. Journal of the Royal Statistical Society, Series C: Applied Statistics 2002; 51(1):91-114. – reference: Zidek JV, Le ND, Wong H, Burnett RT. Including structural measurement errors in the nonlinear regression analysis of clustered data. 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Snippet | Measurement error is pervasive in medical research. In periodontal research studies, one measure of disease status is the probed pocket depth (PPD), the depth... |
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SubjectTerms | Algorithms clustered data Computer Simulation Cross-Sectional Studies Cytokines - analysis Dental care Female Gingival Crevicular Fluid - immunology Gum disease Humans Male measurement error Measurement errors Medical research Medical statistics misclassification Models, Immunological Models, Statistical periodontal disease Periodontal Diseases - immunology SIMEX |
Title | An investigation of the MC-SIMEX method with application to measurement error in periodontal outcomes |
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