Volume 32, Issue 24
Research Article

Logistic‐AFT location‐scale mixture regression models with nonsusceptibility for left‐truncated and general interval‐censored data

Chen‐Hsin Chen

Corresponding Author

Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan

Graduate Institute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei 10055, Taiwan

Correspondence to: Chen‐Hsin Chen, Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan.

E‐mail: chchen@stat.sinica.edu.tw

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Yuh‐Chyuan Tsay

Institute of Statistical Science, Academia Sinica, Taipei 11529, Taiwan

Division of Biometry, Institute of Agronomy, National Taiwan University, Taipei 10764, Taiwan

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Ya‐Chi Wu

Division of Clinical Sciences, Center for Drug Evaluation, Taipei 11557, Taiwan

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Cheng‐Fang Horng

Biostatistics Section, Clinical Protocol Office, Koo Foundation Sun Yat‐Sen Cancer Center, Taipei 11259, Taiwan

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First published: 10 May 2013
Citations: 9

Abstract

In conventional survival analysis there is an underlying assumption that all study subjects are susceptible to the event. In general, this assumption does not adequately hold when investigating the time to an event other than death. Owing to genetic and/or environmental etiology, study subjects may not be susceptible to the disease. Analyzing nonsusceptibility has become an important topic in biomedical, epidemiological, and sociological research, with recent statistical studies proposing several mixture models for right‐censored data in regression analysis. In longitudinal studies, we often encounter left, interval, and right‐censored data because of incomplete observations of the time endpoint, as well as possibly left‐truncated data arising from the dissimilar entry ages of recruited healthy subjects. To analyze these kinds of incomplete data while accounting for nonsusceptibility and possible crossing hazards in the framework of mixture regression models, we utilize a logistic regression model to specify the probability of susceptibility, and a generalized gamma distribution, or a log‐logistic distribution, in the accelerated failure time location‐scale regression model to formulate the time to the event. Relative times of the conditional event time distribution for susceptible subjects are extended in the accelerated failure time location‐scale submodel. We also construct graphical goodness‐of‐fit procedures on the basis of the Turnbull–Frydman estimator and newly proposed residuals. Simulation studies were conducted to demonstrate the validity of the proposed estimation procedure. The mixture regression models are illustrated with alcohol abuse data from the Taiwan Aboriginal Study Project and hypertriglyceridemia data from the Cardiovascular Disease Risk Factor Two‐township Study in Taiwan. Copyright © 2013 John Wiley & Sons, Ltd.

Number of times cited according to CrossRef: 9

  • Semiparametric regression analysis for left-truncated and interval-censored data without or with a cure fraction, Computational Statistics & Data Analysis, 10.1016/j.csda.2019.06.006, (2019).
  • Is Hyperuricemia, an Early-Onset Metabolic Disorder, Causally Associated with Cardiovascular Disease Events in Han Chinese?, Journal of Clinical Medicine, 10.3390/jcm8081202, 8, 8, (1202), (2019).
  • Vertical modeling: analysis of competing risks data with a cure fraction, Lifetime Data Analysis, 10.1007/s10985-018-9417-8, 25, 1, (1-25), (2018).
  • Semiparametric transformation models for interval‐censored data in the presence of a cure fraction, Biometrical Journal, 10.1002/bimj.201700304, 61, 1, (203-215), (2018).
  • Using an Event-History with Risk-Free Model to Study the Genetics of Alcoholism, Scientific Reports, 10.1038/s41598-017-01791-4, 7, 1, (2017).
  • Diagnostic checks in mixture cure models with interval-censoring, Statistical Methods in Medical Research, 10.1177/0962280216676502, 27, 7, (2114-2131), (2016).
  • Heteroscedastic transformation cure regression models, Statistics in Medicine, 10.1002/sim.6896, 35, 14, (2359-2376), (2016).
  • Ages at Onset of 5 Cardiometabolic Diseases Adjusting for Nonsusceptibility: Implications for the Pathogenesis of Metabolic Syndrome, American Journal of Epidemiology, 10.1093/aje/kwv449, 184, 5, (366-377), (2016).
  • Variable selection in a flexible parametric mixture cure model with interval‐censored data, Statistics in Medicine, 10.1002/sim.6767, 35, 7, (1210-1225), (2015).

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