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      Brainstem enlargement in preschool children with autism: Results from an intermethod agreement study of segmentation algorithms

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          Abstract

          The intermethod agreement between automated algorithms for brainstem segmentation is investigated, focusing on the potential involvement of this structure in Autism Spectrum Disorders (ASD). Inconsistencies highlighted in previous studies on brainstem in the population with ASD may in part be a result of poor agreement in the extraction of structural features between different methods. A sample of 76 children with ASD and 76 age‐, gender‐, and intelligence‐matched controls was considered. Volumetric analyses were performed using common tools for brain structures segmentation, namely FSL‐FIRST, FreeSurfer (FS), and Advanced Normalization Tools (ANTs). For shape analysis SPHARM‐MAT was employed. Intermethod agreement was quantified in terms of Pearson correlations between pairs of volumes obtained by the different methods. The degree of overlap between segmented masks was quantified in terms of the Dice index. Both Pearson correlations and Dice indices, showed poor agreement between FSL‐FIRST and the other methods (ANTs and FS), which by contrast, yielded Pearson correlations greater than 0.93 and average Dice indices greater than 0.76 when compared with each other. As with volume, shape analyses exhibited discrepancies between segmentation methods, with particular differences noted between FSL‐FIRST and the others (ANT and FS), with under‐ and over‐segmentation in specific brainstem regions. These data suggest that research on brain structure alterations should cross‐validate findings across multiple methods. We consistently detected an enlargement of brainstem volume in the whole sample and in the male cohort across multiple segmentation methods, a feature particularly driven by the subgroup of children with idiopathic intellectual disability associated with ASD.

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          Most cited references56

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          Open Access Series of Imaging Studies (OASIS): cross-sectional MRI data in young, middle aged, nondemented, and demented older adults.

          The Open Access Series of Imaging Studies is a series of magnetic resonance imaging data sets that is publicly available for study and analysis. The initial data set consists of a cross-sectional collection of 416 subjects aged 18 to 96 years. One hundred of the included subjects older than 60 years have been clinically diagnosed with very mild to moderate Alzheimer's disease. The subjects are all right-handed and include both men and women. For each subject, three or four individual T1-weighted magnetic resonance imaging scans obtained in single imaging sessions are included. Multiple within-session acquisitions provide extremely high contrast-to-noise ratio, making the data amenable to a wide range of analytic approaches including automated computational analysis. Additionally, a reliability data set is included containing 20 subjects without dementia imaged on a subsequent visit within 90 days of their initial session. Automated calculation of whole-brain volume and estimated total intracranial volume are presented to demonstrate use of the data for measuring differences associated with normal aging and Alzheimer's disease.
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            Motor coordination in autism spectrum disorders: a synthesis and meta-analysis.

            Are motor coordination deficits an underlying cardinal feature of Autism Spectrum Disorders (ASD)? Database searches identified 83 ASD studies focused on motor coordination, arm movements, gait, or postural stability deficits. Data extraction involved between-group comparisons for ASD and typically developing controls (N = 51). Rigorous meta-analysis techniques including random effects models, forest and funnel plots, I (2), publication bias, fail-safe analysis, and moderator variable analyses determined a significant standardized mean difference effect equal to 1.20 (SE = 0.144; p <0.0001; Z = 10.49). This large effect indicated substantial motor coordination deficits in the ASD groups across a wide range of behaviors. The current overall findings portray motor coordination deficits as pervasive across diagnoses, thus, a cardinal feature of ASD.
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              Consensus paper: pathological role of the cerebellum in autism.

              There has been significant advancement in various aspects of scientific knowledge concerning the role of cerebellum in the etiopathogenesis of autism. In the current consensus paper, we will observe the diversity of opinions regarding the involvement of this important site in the pathology of autism. Recent emergent findings in literature related to cerebellar involvement in autism are discussed, including: cerebellar pathology, cerebellar imaging and symptom expression in autism, cerebellar genetics, cerebellar immune function, oxidative stress and mitochondrial dysfunction, GABAergic and glutamatergic systems, cholinergic, dopaminergic, serotonergic, and oxytocin-related changes in autism, motor control and cognitive deficits, cerebellar coordination of movements and cognition, gene-environment interactions, therapeutics in autism, and relevant animal models of autism. Points of consensus include presence of abnormal cerebellar anatomy, abnormal neurotransmitter systems, oxidative stress, cerebellar motor and cognitive deficits, and neuroinflammation in subjects with autism. Undefined areas or areas requiring further investigation include lack of treatment options for core symptoms of autism, vermal hypoplasia, and other vermal abnormalities as a consistent feature of autism, mechanisms underlying cerebellar contributions to cognition, and unknown mechanisms underlying neuroinflammation.
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                Author and article information

                Contributors
                paolo.bosco@pi.infn.it
                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
                05 September 2018
                January 2019
                : 40
                : 1 ( doiID: 10.1002/hbm.v40.1 )
                : 7-19
                Affiliations
                [ 1 ] Pisa Division INFN ‐ National Institute for Nuclear Physics Pisa Italy
                [ 2 ] Faculty of Humanities and Social Science University of Strathclyde Glasgow United Kingdom
                [ 3 ] Department of Clinical and Experimental Medicine University of Pisa Pisa Italy
                [ 4 ] IRCCS Stella Maris Foundation Pisa Italy
                Author notes
                [*] [* ] Correspondence

                Pisa Division, INFN ‐ National Institute for Nuclear Physics, Paolo Bosco, Largo Bruno Pontecorvo 3, 56127 Pisa, Italy.

                Email: paolo.bosco@ 123456pi.infn.it

                Author information
                https://orcid.org/0000-0002-4724-9423
                https://orcid.org/0000-0001-5135-4472
                Article
                PMC8022273 PMC8022273 8022273 HBM24351
                10.1002/hbm.24351
                8022273
                30184295
                4edfe2cf-681e-4c86-bd87-eccb1eece019
                © 2018 Wiley Periodicals, Inc.
                History
                : 01 August 2018
                : 02 January 2018
                : 01 August 2018
                Page count
                Figures: 5, Tables: 3, Pages: 13, Words: 11234
                Funding
                Funded by: Tuscany Government (PAR‐FAS 2007‐2013, Bando FAS Salute 2014) through the ARIANNA Project
                Award ID: C52I16000020002
                Funded by: Ministry of Health , open-funder-registry 10.13039/100009647;
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                January 2019
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.1 mode:remove_FC converted:06.04.2021

                brainstem,T1‐weighted MRI,segmentation,brainstem volume,autism spectrum disorders

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