Application of multivariate joint modeling of longitudinal biomarkers and time-to-event data to a rare kidney stone cohort

被引:0
|
作者
Vaughan, Lisa E. E. [1 ]
Lieske, John C. C.
Milliner, Dawn S. S.
Schulte, Phillip J. J. [1 ]
机构
[1] Mayo Clin, Dept Quantitat Hlth Sci, Harwick 8th Floor CT&B Biostat,200 1st St SW, Rochester, MN 55905 USA
关键词
Joint models; survival analysis; biomarkers; kidney failure; primary hyperoxaluria;
D O I
10.1017/cts.2022.465
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background:Time-dependent Cox proportional hazards regression is a popular statistical method used in kidney disease research to evaluate associations between biomarkers collected serially over time with progression to kidney failure. Typically, biomarkers of interest are considered time-dependent covariates being updated at each new measurement using last observation carried forward (LOCF). Recently, joint modeling has emerged as a flexible alternative for multivariate longitudinal and time-to-event data. This study describes and demonstrates multivariate joint modeling using as an example the association of serial biomarkers (plasma oxalate [POX] and urinary oxalate [UOX]) and kidney function among patients with primary hyperoxaluria in the Rare Kidney Stone Consortium Registry. Methods:Time-to-kidney failure was regressed on serially measured biomarkers in two ways: time-dependent LOCF Cox proportional hazards regression and multivariate joint models. Results:In time-dependent LOCF Cox regression, higher POX was associated with increased risk of kidney failure (HR = 2.20 per doubling, 95% CI = [1.38-3.51], p < 0.001) whereas UOX was not (HR = 1.08 per doubling, [0.66-1.77], p = 0.77). In multivariate joint models, estimates suggest higher UOX may be associated with lower risk of kidney failure (HR = 0.42 per doubling [0.15-1.04], p = 0.066), though not statistically significant, since impaired urinary excretion of oxalate may reflect worsening kidney function. Conclusions:Multivariate joint modeling is more flexible than LOCF and may better reflect biological plausibility since biomarkers are not steady-state values between measurements. While LOCF is preferred to naive methods not accounting for changes in biomarkers over time, results may not accurately reflect flexible relationships that can be captured with multivariate joint modeling.
引用
收藏
页数:6
相关论文
共 50 条
  • [31] Choice of baseline hazards in joint modeling of longitudinal and time-to-event cancer survival data
    Hari, Anand
    Jinto, Edakkalathoor George
    Dennis, Divya
    Krishna, Kumarapillai Mohanan Nair Jagathnath
    George, Preethi S.
    Roshni, Sivasevan
    Mathew, Aleyamma
    STATISTICAL APPLICATIONS IN GENETICS AND MOLECULAR BIOLOGY, 2024, 23 (01)
  • [32] FITTING JOINT MODELING OF LONGITUDINAL AND TIME-TO-EVENT DATA USING STOCHASTIC EM APPROACH
    Sabry, Dina M.
    Gad, Ahmed M.
    Mohamed, Ramadan H.
    ADVANCES AND APPLICATIONS IN STATISTICS, 2020, 64 (01) : 33 - 62
  • [33] Joint modeling of multivariate censored longitudinal and event time data with application to the Genetic Markers of Inflammation Study
    Pike, Francis
    Weissfeld, Lisa A.
    Chang, Chung-Chou H.
    JOURNAL OF APPLIED STATISTICS, 2014, 41 (10) : 2178 - 2191
  • [34] Functional joint model for longitudinal and time-to-event data: an application to Alzheimer's disease
    Li, Kan
    Luo, Sheng
    STATISTICS IN MEDICINE, 2017, 36 (22) : 3560 - 3572
  • [35] Joint longitudinal and time-to-event models for multilevel hierarchical data
    Brilleman, Samuel L.
    Crowther, Michael J.
    Moreno-Betancur, Margarita
    Novik, Jacqueline Buros
    Dunyak, James
    Al-Huniti, Nidal
    Fox, Robert
    Hammerbacher, Jeff
    Wolfe, Rory
    STATISTICAL METHODS IN MEDICAL RESEARCH, 2019, 28 (12) : 3502 - 3515
  • [36] Penalized spline joint models for longitudinal and time-to-event data
    Pham Thi Thu Huong
    Nur, Darfiana
    Branford, Alan
    COMMUNICATIONS IN STATISTICS-THEORY AND METHODS, 2017, 46 (20) : 10294 - 10314
  • [37] joineRML: a joint model and software package for time-to-event and multivariate longitudinal outcomes
    Hickey, Graeme L.
    Philipson, Pete
    Jorgensen, Andrea
    Kolamunnage-Dona, Ruwanthi
    BMC MEDICAL RESEARCH METHODOLOGY, 2018, 18
  • [38] Joint modelling of time-to-event and multivariate longitudinal outcomes: recent developments and issues
    Graeme L. Hickey
    Pete Philipson
    Andrea Jorgensen
    Ruwanthi Kolamunnage-Dona
    BMC Medical Research Methodology, 16
  • [39] Joint modelling of time-to-event and multivariate longitudinal outcomes: recent developments and issues
    Hickey, Graeme L.
    Philipson, Pete
    Jorgensen, Andrea
    Kolamunnage-Dona, Ruwanthi
    BMC MEDICAL RESEARCH METHODOLOGY, 2016, 16
  • [40] A Bayesian semiparametric multivariate joint model for multiple longitudinal outcomes and a time-to-event
    Rizopoulos, Dimitris
    Ghosh, Pulak
    STATISTICS IN MEDICINE, 2011, 30 (12) : 1366 - 1380