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Pages 649-659
Received 01 Sep 2015
Accepted author version posted online: 05 Jan 2017
Published online: 08 Feb 2018
 
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ABSTRACT

Existing approaches for multivariate functional principal component analysis are restricted to data on the same one-dimensional interval. The presented approach focuses on multivariate functional data on different domains that may differ in dimension, such as functions and images. The theoretical basis for multivariate functional principal component analysis is given in terms of a Karhunen–Loève Theorem. For the practically relevant case of a finite Karhunen–Loève representation, a relationship between univariate and multivariate functional principal component analysis is established. This offers an estimation strategy to calculate multivariate functional principal components and scores based on their univariate counterparts. For the resulting estimators, asymptotic results are derived. The approach can be extended to finite univariate expansions in general, not necessarily orthonormal bases. It is also applicable for sparse functional data or data with measurement error. A flexible R implementation is available on CRAN. The new method is shown to be competitive to existing approaches for data observed on a common one-dimensional domain. The motivating application is a neuroimaging study, where the goal is to explore how longitudinal trajectories of a neuropsychological test score covary with FDG-PET brain scans at baseline. Supplementary material, including detailed proofs, additional simulation results, and software is available online.

Supplementary Materials

The online appendix contains detailed proofs for all propositions, some additional simulation results, and R code for reproducing the analysis for the ADNI and gait cycle data based on the R packages fundata and MFPCA (Happ 2017a Happ, C. (2017a), funData: An S4 Class for Functional Data in R, R Package Version 1.0. [Google Scholar], 2017b ——— (2017b), MFPCA: Multivariate Functional Principal Component Analysis, R Package Version 1.0-1. [Google Scholar]).

Acknowledgments

Data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (http://adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this article. A complete listing of ADNI investigators can be found at: http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf. A detailed list of ADNI funding is available at http://adni.loni.usc.edu/about/funding/.

Additional information

Funding

The authors acknowledge support from the German Research Foundation through Emmy Noether grant GR 3793/1-1 and would like to thank the LMUMentoring program for financial support to cover the printing costs. Data collection and sharing for the neuroimaging data in Section 5 was funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI, National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Disease Cooperative Study at the University of California, San Diego. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California.

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