Modeling longitudinal count data with dropouts

被引:2
|
作者
Alosh, Mohamed [1 ]
机构
[1] US FDA, Div Biometr 3, OB, OTS,CDER, Silver Spring, MD USA
关键词
covariate-dependent dropouts; generalized Poisson autoregressive model; generalized mixed effects model; GEE; weighted GEE; MISSING DATA;
D O I
10.1002/pst.366
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This paper explores the utility of different approaches for modeling longitudinal count data with dropouts arising from a clinical study for the treatment of actinic keratosis lesions on the face and balding scalp. A feature of these data is that as the disease for subjects on the active arm improves their data show larger dispersion compared with those on the vehicle, exhibiting an over-dispersion relative to the Poisson distribution. After fitting the marginal (or population averaged) model using the generalized estimating equation (GEE), we note that inferences from such a model might be biased as dropouts are treatment related. Then, we consider using a weighted GEE (WGEE) where each subject's contribution to the analysis is weighted inversely by the subject's probability of dropout. Based on the model findings, we argue that the WGEE might not address the concerns about the impact of dropouts on the efficacy findings when dropouts are treatment related. As an alternative, we consider likelihood-based inference where random effects are added to the model to allow for heterogeneity across subjects. Finally, we consider a transition model where, unlike the previous approaches that model the log-link function of the mean response, we model the subject's actual lesion counts. This model is an extension of the Poisson autoregressive model of order 1, where the autoregressive parameter is taken to he a function of treatment as well as other covariates to induce different dispersions and correlations for the two treatment arms. We conclude with a discussion about model selection. Published in 2009 by John Wiley & Sons, Ltd.
引用
收藏
页码:35 / 45
页数:11
相关论文
共 50 条
  • [31] Quantile Regression For Longitudinal Biomarker Data Subject to Left Censoring and Dropouts
    Lee, Minjae
    Kong, Lan
    COMMUNICATIONS IN STATISTICS-THEORY AND METHODS, 2014, 43 (21) : 4628 - 4641
  • [32] A joint mean-correlation modeling approach for longitudinal zero-inflated count data
    Zhang, Weiping
    Wang, Jiangli
    Qian, Fang
    Chen, Yu
    BRAZILIAN JOURNAL OF PROBABILITY AND STATISTICS, 2020, 34 (01) : 35 - 50
  • [33] Bayesian Model Selection for Longitudinal Count Data
    Oludare Ariyo
    Emmanuel Lesaffre
    Geert Verbeke
    Adrian Quintero
    Sankhya B, 2022, 84 : 516 - 547
  • [34] Bayesian quantile regression for longitudinal count data
    Jantre, Sanket
    JOURNAL OF STATISTICAL COMPUTATION AND SIMULATION, 2023, 93 (01) : 103 - 127
  • [35] Analyzing Unevenly Spaced Longitudinal Count Data
    Oyet A.J.
    Sutradhar B.C.
    Sankhya B, 2021, 83 (2) : 342 - 373
  • [36] Bayesian Model Selection for Longitudinal Count Data
    Ariyo, Oludare
    Lesaffre, Emmanuel
    Verbeke, Geert
    Quintero, Adrian
    SANKHYA-SERIES B-APPLIED AND INTERDISCIPLINARY STATISTICS, 2022, 84 (02): : 516 - 547
  • [37] Analysis of longitudinal count data with serial correlation
    Xu, Stanley
    Jones, Richard H.
    Grunwald, Gary K.
    BIOMETRICAL JOURNAL, 2007, 49 (03) : 416 - 428
  • [38] Analyzing Unevenly Spaced Longitudinal Count Data
    Oyet, Alwell J.
    Sutradhar, Brajendra C.
    SANKHYA-SERIES B-APPLIED AND INTERDISCIPLINARY STATISTICS, 2021, 83 (02): : 342 - 373
  • [39] Likelihood approach for count data in longitudinal experiments
    Gonçalves, M. Helena
    Salomé Cabral, M.
    Carme Ruiz de Villa, Maria
    Escrich, Eduardo
    Solanas, Montse
    Computational Statistics and Data Analysis, 2007, 51 (12): : 6511 - 6520
  • [40] Analysis of Zero-Inflated Count Data From Clinical Trials With Potential Dropouts
    Yang, Jingyuan
    Li, Xiaoming
    Liu, Guanghan F.
    STATISTICS IN BIOPHARMACEUTICAL RESEARCH, 2012, 4 (03): : 273 - 283