4.5 Article

Joint longitudinal hurdle and time-to-event models: an application related to viral load and duration of the first treatment regimen in patients with HIV initiating therapy

Journal

STATISTICS IN MEDICINE
Volume 35, Issue 20, Pages 3583-3594

Publisher

WILEY-BLACKWELL
DOI: 10.1002/sim.6948

Keywords

joint model; shared parameter model; hurdle model; detection limit; censoring

Funding

  1. National Institute for Health Research (NIHR)
  2. NIHR Methods Fellowship [MET 12-20]
  3. NIHR Doctoral Research Fellowship [DRF-2012-05-409]
  4. UK Medical Research Council (MRC) [MR/J002380/1]
  5. UK Department for International Development (DFID) under the MRC/DFID
  6. EDCTP2 programme - European Union
  7. MRC [MR/J002380/1] Funding Source: UKRI
  8. Medical Research Council [MR/J002380/1] Funding Source: researchfish
  9. National Institute for Health Research [NF-SI-0611-10168, DRF-2012-05-409, MET-12-20-101, NF-SI-0512-10159] Funding Source: researchfish

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Shared parameter joint models provide a framework under which a longitudinal response and a time to event can be modelled simultaneously. A common assumption in shared parameter joint models has been to assume that the longitudinal response is normally distributed. In this paper, we instead propose a joint model that incorporates a two-part hurdle' model for the longitudinal response, motivated in part by longitudinal response data that is subject to a detection limit. The first part of the hurdle model estimates the probability that the longitudinal response is observed above the detection limit, whilst the second part of the hurdle model estimates the mean of the response conditional on having exceeded the detection limit. The time-to-event outcome is modelled using a parametric proportional hazards model, assuming a Weibull baseline hazard. We propose a novel association structure whereby the current hazard of the event is assumed to be associated with the current combined (expected) outcome from the two parts of the hurdle model. We estimate our joint model under a Bayesian framework and provide code for fitting the model using the Bayesian software Stan. We use our model to estimate the association between HIV RNA viral load, which is subject to a lower detection limit, and the hazard of stopping or modifying treatment in patients with HIV initiating antiretroviral therapy. Copyright (c) 2016 John Wiley & Sons, Ltd.

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