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arXiv 2201.09753cs.LGstat.APstat.CO

Evaluation of data imputation strategies in complex, deeply-phenotyped data sets: the case of the EU-AIMS Longitudinal European Autism Project

Radboud University Medical Centre(拉德堡德大学医学中心);LIS data solutions(LIS数据解决方案公司);University of Zurich(苏黎世大学);Karakter Child and Adolescent Psychiatry University Centre(Karakter儿童与青少年精神病学大学中心);University of Heidelberg(海德堡大学);SRH University(SRH大学);Goethe University(法兰克福大学);University of Cambridge(剑桥大学);University Medical Center Utrecht(乌得勒支大学医学中心);University of Oxford(牛津大学)
A. Llera, M. Brammer, B. Oakley, J. Tillmann, M. Zabihi, T. Mei, T. Charman, C. Ecker, F. Dell Acqua, T. Banaschewski, C. Moessnang, S. Baron-Cohen, R. Holt, S.… 展开作者

A. Llera, M. Brammer, B. Oakley, J. Tillmann, M. Zabihi, T. Mei, T. Charman, C. Ecker, F. Dell Acqua, T. Banaschewski, C. Moessnang, S. Baron-Cohen, R. Holt, S. Durston, D. Murphy, E. Loth, J. K. Buitelaar, D. L. Floris, C. F. Beckmann

英文摘要:

An increasing number of large-scale multi-modal research initiatives has been conducted in the typically developing population, as well as in psychiatric cohorts. Missing data is a common problem in such datasets due to the difficulty of assessing multiple measures on a large number of participants. The consequences of missing data accumulate when researchers aim to explore relationships between multiple measures. Here we aim to evaluate different imputation strategies to fill in missing values in clinical data from a large (total N=764) and deeply characterised (i.e. range of clinical and cognitive instruments administered) sample of N=453 autistic individuals and N=311 control individuals recruited as part of the EU-AIMS Longitudinal European Autism Project (LEAP) consortium. In particular we consider a total of 160 clinical measures divided in 15 overlapping subsets of participants. We use two simple but common univariate strategies, mean and median imputation, as well as a Round Robin regression approach involving four independent multivariate regression models including a linear model, Bayesian Ridge regression, as well as several non-linear models, Decision Trees, Extra Trees and K-Neighbours regression. We evaluate the models using the traditional mean square error towards removed available data, and consider in addition the KL divergence between the observed and the imputed distributions. We show that all of the multivariate approaches tested provide a substantial improvement compared to typical univariate approaches. Further, our analyses reveal that across all 15 data-subsets tested, an Extra Trees regression approach provided the best global results. This allows the selection of a unique model to impute missing data for the LEAP project and deliver a fixed set of imputed clinical data to be used by researchers working with the LEAP dataset in the future.

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