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      Prediction of Verbal Abilities From Brain Connectivity Data Across the Lifespan Using a Machine Learning Approach

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          ABSTRACT

          Compared to nonverbal cognition such as executive or memory functions, language‐related cognition generally appears to remain more stable until later in life. Nevertheless, different language‐related processes, for example, verbal fluency versus vocabulary knowledge, appear to show different trajectories across the life span. One potential explanation for differences in verbal functions may be alterations in the functional and structural network architecture of different large‐scale brain networks. For example, differences in verbal abilities have been linked to the communication within and between the frontoparietal (FPN) and default mode network (DMN). It, however, remains open whether brain connectivity within these networks may be informative for language performance at the individual level across the life span. Further information in this regard may be highly desirable as verbal abilities allow us to participate in daily activities, are associated with quality of life, and may be considered in preventive and interventional setups to foster cognitive health across the life span. So far, mixed prediction results based on resting‐state functional connectivity (FC) and structural connectivity (SC) data have been reported for language abilities across different samples, age groups, and machine‐learning (ML) approaches. Therefore, the current study set out to investigate the predictability of verbal fluency and vocabulary knowledge based on brain connectivity data in the DMN, FPN, and the whole brain using an ML approach in a lifespan sample ( N = 717; age range: 18–85) from the 1000BRAINS study. Prediction performance was, thereby, systematically compared across (i) verbal [verbal fluency and vocabulary knowledge] and nonverbal abilities [processing speed and visual working memory], (ii) modalities [FC and SC data], (iii) feature sets [DMN, FPN, DMN‐FPN, and whole brain], and (iv) samples [total, younger, and older aged group]. Results from the current study showed that verbal abilities could not be reliably predicted from FC and SC data across feature sets and samples. Thereby, no predictability differences emerged between verbal fluency and vocabulary knowledge across input modalities, feature sets, and samples. In contrast to verbal functions, nonverbal abilities could be moderately predicted from connectivity data, particularly SC, in the total and younger age group. Satisfactory prediction performance for nonverbal cognitive functions based on currently chosen connectivity data was, however, not encountered in the older age group. Current results, hence, emphasized that verbal functions may be more difficult to predict from brain connectivity data in domain‐general cognitive networks and the whole brain compared to nonverbal abilities, particularly executive functions, across the life span. Thus, it appears warranted to more closely investigate differences in predictability between different cognitive functions and age groups.

          Abstract

          Functional and structural connectivity data was used to predict verbal fluency and vocabulary knowledge in a lifespan sample using two machine learning algorithms. The predictability of verbal compared to nonverbal abilities in younger and older adults was found to be low across whole‐brain and network‐specific functional and structural imaging data.

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          Most cited references125

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          FSL.

          FSL (the FMRIB Software Library) is a comprehensive library of analysis tools for functional, structural and diffusion MRI brain imaging data, written mainly by members of the Analysis Group, FMRIB, Oxford. For this NeuroImage special issue on "20 years of fMRI" we have been asked to write about the history, developments and current status of FSL. We also include some descriptions of parts of FSL that are not well covered in the existing literature. We hope that some of this content might be of interest to users of FSL, and also maybe to new research groups considering creating, releasing and supporting new software packages for brain image analysis. Copyright © 2011 Elsevier Inc. All rights reserved.
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            The organization of the human cerebral cortex estimated by intrinsic functional connectivity.

            Information processing in the cerebral cortex involves interactions among distributed areas. Anatomical connectivity suggests that certain areas form local hierarchical relations such as within the visual system. Other connectivity patterns, particularly among association areas, suggest the presence of large-scale circuits without clear hierarchical relations. In this study the organization of networks in the human cerebrum was explored using resting-state functional connectivity MRI. Data from 1,000 subjects were registered using surface-based alignment. A clustering approach was employed to identify and replicate networks of functionally coupled regions across the cerebral cortex. The results revealed local networks confined to sensory and motor cortices as well as distributed networks of association regions. Within the sensory and motor cortices, functional connectivity followed topographic representations across adjacent areas. In association cortex, the connectivity patterns often showed abrupt transitions between network boundaries. Focused analyses were performed to better understand properties of network connectivity. A canonical sensory-motor pathway involving primary visual area, putative middle temporal area complex (MT+), lateral intraparietal area, and frontal eye field was analyzed to explore how interactions might arise within and between networks. Results showed that adjacent regions of the MT+ complex demonstrate differential connectivity consistent with a hierarchical pathway that spans networks. The functional connectivity of parietal and prefrontal association cortices was next explored. Distinct connectivity profiles of neighboring regions suggest they participate in distributed networks that, while showing evidence for interactions, are embedded within largely parallel, interdigitated circuits. We conclude by discussing the organization of these large-scale cerebral networks in relation to monkey anatomy and their potential evolutionary expansion in humans to support cognition.
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              Local-Global Parcellation of the Human Cerebral Cortex from Intrinsic Functional Connectivity MRI.

              A central goal in systems neuroscience is the parcellation of the cerebral cortex into discrete neurobiological "atoms". Resting-state functional magnetic resonance imaging (rs-fMRI) offers the possibility of in vivo human cortical parcellation. Almost all previous parcellations relied on 1 of 2 approaches. The local gradient approach detects abrupt transitions in functional connectivity patterns. These transitions potentially reflect cortical areal boundaries defined by histology or visuotopic fMRI. By contrast, the global similarity approach clusters similar functional connectivity patterns regardless of spatial proximity, resulting in parcels with homogeneous (similar) rs-fMRI signals. Here, we propose a gradient-weighted Markov Random Field (gwMRF) model integrating local gradient and global similarity approaches. Using task-fMRI and rs-fMRI across diverse acquisition protocols, we found gwMRF parcellations to be more homogeneous than 4 previously published parcellations. Furthermore, gwMRF parcellations agreed with the boundaries of certain cortical areas defined using histology and visuotopic fMRI. Some parcels captured subareal (somatotopic and visuotopic) features that likely reflect distinct computational units within known cortical areas. These results suggest that gwMRF parcellations reveal neurobiologically meaningful features of brain organization and are potentially useful for future applications requiring dimensionality reduction of voxel-wise fMRI data. Multiresolution parcellations generated from 1489 participants are publicly available (https://github.com/ThomasYeoLab/CBIG/tree/master/stable_projects/brain_parcellation/Schaefer2018_LocalGlobal).
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                Author and article information

                Contributors
                svenja.caspers@hhu.de
                Journal
                Hum Brain Mapp
                Hum Brain Mapp
                10.1002/(ISSN)1097-0193
                HBM
                Human Brain Mapping
                John Wiley & Sons, Inc. (Hoboken, USA )
                1065-9471
                1097-0193
                25 March 2025
                1 April 2025
                : 46
                : 5 ( doiID: 10.1002/hbm.v46.5 )
                : e70191
                Affiliations
                [ 1 ] Institute of Neuroscience and Medicine (INM‐1) Research Centre Jülich Jülich Germany
                [ 2 ] Institute for Anatomy I, Medical Faculty & University Hospital Düsseldorf Heinrich Heine University Düsseldorf Düsseldorf Germany
                [ 3 ] Institute of Neuroscience and Medicine, Brain and Behaviour (INM‐7) Research Centre Jülich Jülich Germany
                [ 4 ] Institute of Systems Neuroscience, Medical Faculty & University Hospital Düsseldorf Heinrich Heine University Düsseldorf Düsseldorf Germany
                Author notes
                [*] [* ] Correspondence:

                Svenja Caspers ( svenja.caspers@ 123456hhu.de )

                Article
                HBM70191 HBM-24-0920.R1
                10.1002/hbm.70191
                11933761
                40130301
                d90668d2-db18-48ee-a4a0-b3a1d5b69180
                © 2025 The Author(s). Human Brain Mapping published by Wiley Periodicals LLC.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 27 January 2025
                : 05 September 2024
                : 02 March 2025
                Page count
                Figures: 5, Tables: 3, Pages: 19, Words: 16000
                Funding
                Funded by: European Union’s Horizon 2020 Research and Innovation Program
                Award ID: 101147319
                Categories
                Research Article
                Research Article
                Custom metadata
                2.0
                April 1, 2025
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.5.4 mode:remove_FC converted:25.03.2025

                Neurology
                connectivity,language functions,life span,ml analyses,prediction
                Neurology
                connectivity, language functions, life span, ml analyses, prediction

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