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      Generalized multilevel function-on-scalar regression and principal component analysis : Generalized Multilevel Function-on-Scalar Regression and Principal Component Analysis

      1 , 2 , 3 , 4
      Biometrics
      Wiley

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          Abstract

          This manuscript considers regression models for generalized, multilevel functional responses: functions are generalized in that they follow an exponential family distribution and multilevel in that they are clustered within groups or subjects. This data structure is increasingly common across scientific domains and is exemplified by our motivating example, in which binary curves indicating physical activity or inactivity are observed for nearly 600 subjects over 5 days. We use a generalized linear model to incorporate scalar covariates into the mean structure, and decompose subject-specific and subject-day-specific deviations using multilevel functional principal components analysis. Thus, functional fixed effects are estimated while accounting for within-function and within-subject correlations, and major directions of variability within and between subjects are identified. Fixed effect coefficient functions and principal component basis functions are estimated using penalized splines; model parameters are estimated in a Bayesian framework using Stan, a programming language that implements a Hamiltonian Monte Carlo sampler. Simulations designed to mimic the application have good estimation and inferential properties with reasonable computation times for moderate datasets, in both cross-sectional and multilevel scenarios; code is publicly available. In the application we identify effects of age and BMI on the time-specific change in probability of being active over a 24-hour period; in addition, the principal components analysis identifies the patterns of activity that distinguish subjects and days within subjects.

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          Functional Data Analysis for Sparse Longitudinal Data

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            Patterns of accelerometer-assessed sedentary behavior in older women.

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              Functional mixed effects models.

              In this article, a new class of functional models in which smoothing splines are used to model fixed effects as well as random effects is introduced. The linear mixed effects models are extended to nonparametric mixed effects models by introducing functional random effects, which are modeled as realizations of zero-mean stochastic processes. The fixed functional effects and the random functional effects are modeled in the same functional space, which guarantee the population-average and subject-specific curves have the same smoothness property. These models inherit the flexibility of the linear mixed effects models in handling complex designs and correlation structures, can include continuous covariates as well as dummy factors in both the fixed or random design matrices, and include the nested curves models as special cases. Two estimation procedures are proposed. The first estimation procedure exploits the connection between linear mixed effects models and smoothing splines and can be fitted using existing software. The second procedure is a sequential estimation procedure using Kalman filtering. This algorithm avoids inversion of large dimensional matrices and therefore can be applied to large data sets. A generalized maximum likelihood (GML) ratio test is proposed for inference and model selection. An application to comparison of cortisol profiles is used as an illustration.
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                Author and article information

                Journal
                Biometrics
                Biom
                Wiley
                0006341X
                June 2015
                June 2015
                January 25 2015
                : 71
                : 2
                : 344-353
                Affiliations
                [1 ]Department of Biostatistics, Mailman School of Public Health; Columbia University; New York New York U.S.A.
                [2 ]Department of Biostatistics, Bloomberg School of Public Health; Johns Hopkins University; Baltimore Maryland U.S.A.
                [3 ]Department of Epidemiology, Bloomberg School of Public Health; Johns Hopkins University; Baltimore Maryland U.S.A.
                [4 ]Longitudinal Studies Section, Translational Gerontology Branch, National Institute on Aging; National Institutes of Health; Bethesda Maryland U.S.A.
                Article
                10.1111/biom.12278
                4479975
                25620473
                350d236a-a4b2-4b34-ae7b-62056f592bae
                © 2015

                http://doi.wiley.com/10.1002/tdm_license_1.1

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