TY - JOUR
T1 - A novel quantification of information for longitudinal data analyzed by mixed-effects modeling
AU - Yuan, Min
AU - Li, Yi
AU - Yang, Yaning
AU - Xu, Jinfeng
AU - Tao, Fangbiao
AU - Zhao, Liang
AU - Zhou, Honghui
AU - Pinheiro, Jose
AU - Xu, Xu Steven
PY - 2020/7
Y1 - 2020/7
N2 - Nonlinear mixed-effects (NLME) modeling is one of the most powerful tools for analyzing longitudinal data especially under the sparse sampling design. The determinant of the Fisher information matrix is a commonly used global metric of the information that can be provided by the data under a given model. However, in clinical studies, it is also important to measure how much information the data provide for a certain parameter of interest under the assumed model, for example, the clearance in population pharmacokinetic models. This paper proposes a new, easy-to-interpret information metric, the “relative information” (RI), which is designed for specific parameters of a model and takes a value between 0% and 100%. We establish the relationship between interindividual variability for a specific parameter and the variance of the associated parameter estimator, demonstrating that, under a “perfect” experiment (eg, infinite samples or/and minimum experimental error), the RI and the variance of the model parameter estimator converge, respectively, to 100% and the ratio of the interindividual variability for that parameter and the number of subjects. Extensive simulation experiments and analyses of three real datasets show that our proposed RI metric can accurately characterize the information for parameters of interest for NLME models. The new information metric can be readily used to facilitate study designs and model diagnosis.
AB - Nonlinear mixed-effects (NLME) modeling is one of the most powerful tools for analyzing longitudinal data especially under the sparse sampling design. The determinant of the Fisher information matrix is a commonly used global metric of the information that can be provided by the data under a given model. However, in clinical studies, it is also important to measure how much information the data provide for a certain parameter of interest under the assumed model, for example, the clearance in population pharmacokinetic models. This paper proposes a new, easy-to-interpret information metric, the “relative information” (RI), which is designed for specific parameters of a model and takes a value between 0% and 100%. We establish the relationship between interindividual variability for a specific parameter and the variance of the associated parameter estimator, demonstrating that, under a “perfect” experiment (eg, infinite samples or/and minimum experimental error), the RI and the variance of the model parameter estimator converge, respectively, to 100% and the ratio of the interindividual variability for that parameter and the number of subjects. Extensive simulation experiments and analyses of three real datasets show that our proposed RI metric can accurately characterize the information for parameters of interest for NLME models. The new information metric can be readily used to facilitate study designs and model diagnosis.
KW - Fisher information
KW - longitudinal data
KW - nonlinear mixed-effects model
KW - relative information
UR - http://www.scopus.com/inward/record.url?scp=85078729020&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85078729020&origin=recordpage
U2 - 10.1002/pst.1996
DO - 10.1002/pst.1996
M3 - RGC 21 - Publication in refereed journal
C2 - 31989784
SN - 1539-1604
VL - 19
SP - 388
EP - 398
JO - Pharmaceutical Statistics
JF - Pharmaceutical Statistics
IS - 4
ER -