Literature DB >> 29948579

New approaches for censored longitudinal data in joint modelling of longitudinal and survival data, with application to HIV vaccine studies.

Tingting Yu1, Lang Wu2, Peter Gilbert3,4.   

Abstract

In HIV vaccine studies, longitudinal immune response biomarker data are often left-censored due to lower limits of quantification of the employed immunological assays. The censoring information is important for predicting HIV infection, the failure event of interest. We propose two approaches to addressing left censoring in longitudinal data: one that makes no distributional assumptions for the censored data-treating left censored values as a "point mass" subgroup-and the other makes a distributional assumption for a subset of the censored data but not for the remaining subset. We develop these two approaches to handling censoring for joint modelling of longitudinal and survival data via a Cox proportional hazards model fit by h-likelihood. We evaluate the new methods via simulation and analyze an HIV vaccine trial data set, finding that longitudinal characteristics of the immune response biomarkers are highly associated with the risk of HIV infection.

Entities:  

Keywords:  Cox model; H-likelihood; Lower limit of quantification; Mixed-effect model; Shared-parameter model

Mesh:

Substances:

Year:  2018        PMID: 29948579      PMCID: PMC6286694          DOI: 10.1007/s10985-018-9434-7

Source DB:  PubMed          Journal:  Lifetime Data Anal        ISSN: 1380-7870            Impact factor:   1.588


  10 in total

1.  Mixed effects models with censored data with application to HIV RNA levels.

Authors:  J P Hughes
Journal:  Biometrics       Date:  1999-06       Impact factor: 2.571

2.  Repeated measures with zeros.

Authors:  K N Berk; P A Lachenbruch
Journal:  Stat Methods Med Res       Date:  2002-08       Impact factor: 3.021

3.  Analysis of data with excess zeros.

Authors:  Peter A Lachenbruch
Journal:  Stat Methods Med Res       Date:  2002-08       Impact factor: 3.021

4.  Analysing microbiological data: Tobit or not Tobit?

Authors:  M F Lorimer; A Kiermeier
Journal:  Int J Food Microbiol       Date:  2007-02-14       Impact factor: 5.277

5.  A joint model for mixed and truncated longitudinal data and survival data, with application to HIV vaccine studies.

Authors:  Tingting Yu; Lang Wu; Peter B Gilbert
Journal:  Biostatistics       Date:  2018-07-01       Impact factor: 5.899

6.  A mixture model with detection limits for regression analyses of antibody response to vaccine.

Authors:  L H Moulton; N A Halsey
Journal:  Biometrics       Date:  1995-12       Impact factor: 2.571

7.  Correlation between immunologic responses to a recombinant glycoprotein 120 vaccine and incidence of HIV-1 infection in a phase 3 HIV-1 preventive vaccine trial.

Authors:  Peter B Gilbert; Michael L Peterson; Dean Follmann; Michael G Hudgens; Donald P Francis; Marc Gurwith; William L Heyward; David V Jobes; Vladimir Popovic; Steven G Self; Faruk Sinangil; Donald Burke; Phillip W Berman
Journal:  J Infect Dis       Date:  2005-01-27       Impact factor: 5.226

8.  Analysis of left-censored longitudinal data with application to viral load in HIV infection.

Authors:  H Jacqmin-Gadda; R Thiébaut; G Chêne; D Commenges
Journal:  Biostatistics       Date:  2000-12       Impact factor: 5.899

9.  Bayesian semiparametric mixture Tobit models with left censoring, skewness, and covariate measurement errors.

Authors:  Getachew A Dagne; Yangxin Huang
Journal:  Stat Med       Date:  2013-04-02       Impact factor: 2.373

10.  Joint modelling of bivariate longitudinal data with informative dropout and left-censoring, with application to the evolution of CD4+ cell count and HIV RNA viral load in response to treatment of HIV infection.

Authors:  Rodolphe Thiébaut; Hélène Jacqmin-Gadda; Abdel Babiker; Daniel Commenges
Journal:  Stat Med       Date:  2005-01-15       Impact factor: 2.373

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.