Abstract

Neuroimaging-driven prediction of brain age, defined as the predicted biological age of a subject using only brain imaging data, is an exciting avenue of research. In this work we seek to build models of brain age based on functional connectivity while prioritizing model interpretability and understanding. This way, the models serve to both provide accurate estimates of brain age as well as allow us to investigate changes in functional connectivity which occur during the ageing process. The methods proposed in this work consist of a two-step procedure: first, linear latent variable models, such as PCA and its extensions, are employed to learn reproducible functional connectivity networks present across a cohort of subjects. The activity within each network is subsequently employed as a feature in a linear regression model to predict brain age. The proposed framework is employed on the data from the CamCAN repository and the inferred brain age models are further demonstrated to generalize using data from two open-access repositories: the Human Connectome Project and the ATR Wide-Age-Range.

Highlights

  • The human brain changes during the lifespan of an adult, resulting in robust and reproducible changes in structure and function [1, 2]

  • Due to our focus on interpretability, we focus on linear latent variable models, such as principal component analysis (PCA), independent component analysis (ICA) and their generalizations

  • We study the performance across the following methods: factor analysis (FA), PCA, non-negative PCA [27], MCF [26] and Modular Hierarchical Analysis (MHA) [29] as well as ICA

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Summary

Introduction

The human brain changes during the lifespan of an adult, resulting in robust and reproducible changes in structure and function [1, 2]. There is reason to hypothesize that deviations from the typical brain ageing trajectory may reflect latent neuropathological influences [3], serving to motivate further research into developing reliable biomarkers derived from brain imaging data. With respect to the HCP data, we studied resting state fMRI data from HCP Young Adult dataset: https://www.humanconnectome.org/study/hcpyoung-adult/document/1200-subjects-datarelease. With respect to the ATR Wide-Age-Range data, the resting state fMRI data was studied: https://bicr-resource.atr.jp/impact/

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