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      Automated temporalis muscle quantification and growth charts for children through adulthood

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          Abstract

          Lean muscle mass (LMM) is an important aspect of human health. Temporalis muscle thickness is a promising LMM marker but has had limited utility due to its unknown normal growth trajectory and reference ranges and lack of standardized measurement. Here, we develop an automated deep learning pipeline to accurately measure temporalis muscle thickness (iTMT) from routine brain magnetic resonance imaging (MRI). We apply iTMT to 23,876 MRIs of healthy subjects, ages 4 through 35, and generate sex-specific iTMT normal growth charts with percentiles. We find that iTMT was associated with specific physiologic traits, including caloric intake, physical activity, sex hormone levels, and presence of malignancy. We validate iTMT across multiple demographic groups and in children with brain tumors and demonstrate feasibility for individualized longitudinal monitoring. The iTMT pipeline provides unprecedented insights into temporalis muscle growth during human development and enables the use of LMM tracking to inform clinical decision-making.

          Abstract

          Temporalis muscle thickness is a promising marker of lean muscle mass but has had limited utility due to its unknown normal growth trajectory and lack of standardized measurement. Here, the authors develop an automated deep learning pipeline to accurately measure temporalis muscle thickness from routine brain magnetic resonance imaging.

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          Most cited references67

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          Sarcopenia

          Sarcopenia is a progressive and generalised skeletal muscle disorder involving the accelerated loss of muscle mass and function that is associated with increased adverse outcomes including falls, functional decline, frailty, and mortality. It occurs commonly as an age-related process in older people, influenced not only by contemporaneous risk factors, but also by genetic and lifestyle factors operating across the life course. It can also occur in mid-life in association with a range of conditions. Sarcopenia has become the focus of intense research aiming to translate current knowledge about its pathophysiology into improved diagnosis and treatment, with particular interest in the development of biomarkers, nutritional interventions, and drugs to augment the beneficial effects of resistance exercise. Designing effective preventive strategies that people can apply during their lifetime is of primary concern. Diagnosis, treatment, and prevention of sarcopenia is likely to become part of routine clinical practice.
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            The Adolescent Brain Cognitive Development (ABCD) study: Imaging acquisition across 21 sites

            The ABCD study is recruiting and following the brain development and health of over 10,000 9–10 year olds through adolescence. The imaging component of the study was developed by the ABCD Data Analysis and Informatics Center (DAIC) and the ABCD Imaging Acquisition Workgroup. Imaging methods and assessments were selected, optimized and harmonized across all 21 sites to measure brain structure and function relevant to adolescent development and addiction. This article provides an overview of the imaging procedures of the ABCD study, the basis for their selection and preliminary quality assurance and results that provide evidence for the feasibility and age-appropriateness of procedures and generalizability of findings to the existent literature.
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              Unbiased average age-appropriate atlases for pediatric studies.

              Spatial normalization, registration, and segmentation techniques for Magnetic Resonance Imaging (MRI) often use a target or template volume to facilitate processing, take advantage of prior information, and define a common coordinate system for analysis. In the neuroimaging literature, the MNI305 Talairach-like coordinate system is often used as a standard template. However, when studying pediatric populations, variation from the adult brain makes the MNI305 suboptimal for processing brain images of children. Morphological changes occurring during development render the use of age-appropriate templates desirable to reduce potential errors and minimize bias during processing of pediatric data. This paper presents the methods used to create unbiased, age-appropriate MRI atlas templates for pediatric studies that represent the average anatomy for the age range of 4.5-18.5 years, while maintaining a high level of anatomical detail and contrast. The creation of anatomical T1-weighted, T2-weighted, and proton density-weighted templates for specific developmentally important age-ranges, used data derived from the largest epidemiological, representative (healthy and normal) sample of the U.S. population, where each subject was carefully screened for medical and psychiatric factors and characterized using established neuropsychological and behavioral assessments. Use of these age-specific templates was evaluated by computing average tissue maps for gray matter, white matter, and cerebrospinal fluid for each specific age range, and by conducting an exemplar voxel-wise deformation-based morphometry study using 66 young (4.5-6.9 years) participants to demonstrate the benefits of using the age-appropriate templates. The public availability of these atlases/templates will facilitate analysis of pediatric MRI data and enable comparison of results between studies in a common standardized space specific to pediatric research. Copyright © 2010 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                Benjamin_Kann@dfci.harvard.edu
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                9 November 2023
                9 November 2023
                2023
                : 14
                : 6863
                Affiliations
                [1 ]GRID grid.38142.3c, ISNI 000000041936754X, Artificial Intelligence in Medicine (AIM) Program, Mass General Brigham, , Harvard Medical School, ; Boston, MA USA
                [2 ]GRID grid.38142.3c, ISNI 000000041936754X, Department of Radiation Oncology, Dana-Farber Cancer Institute, Brigham and Women’s Hospital, Boston Children’s Hospital, , Harvard Medical School, ; Boston, MA USA
                [3 ]Department of Data Science, Dana-Farber Cancer Institute, ( https://ror.org/02jzgtq86) Boston, MA USA
                [4 ]GRID grid.38142.3c, ISNI 000000041936754X, Department of Biostatistics, , Harvard T.H. Chan School of Public Health, ; Boston, MA USA
                [5 ]GRID grid.38142.3c, ISNI 000000041936754X, Dana-Farber/Boston Children’s Cancer and Blood Disorders Center, Harvard Medical School, ; Boston, MA USA
                [6 ]Michigan State University, ( https://ror.org/05hs6h993) East Lansing, MI USA
                [7 ]Department of Radiology, Boston Children’s Hospital, ( https://ror.org/00dvg7y05) Boston, MA USA
                [8 ]Children’s Hospital of Philadelphia, ( https://ror.org/01z7r7q48) Philadelphia, USA
                [9 ]University of Pennsylvania, ( https://ror.org/00b30xv10) Pennsylvania, USA
                [10 ]GRID grid.266102.1, ISNI 0000 0001 2297 6811, Department of Neurology, Neurosurgery and Pediatrics, , University of California, ; San Francisco, USA
                [11 ]Department of Radiology and Nuclear Medicine, CARIM & GROW, Maastricht University, ( https://ror.org/02jz4aj89) Maastricht, the Netherlands
                Author information
                http://orcid.org/0000-0001-6860-9160
                http://orcid.org/0009-0007-7563-6045
                http://orcid.org/0000-0002-1782-1919
                http://orcid.org/0000-0002-9315-8653
                http://orcid.org/0000-0002-8754-0565
                http://orcid.org/0000-0002-8216-9357
                http://orcid.org/0000-0002-2378-4800
                http://orcid.org/0000-0002-2122-2003
                http://orcid.org/0000-0002-4313-2754
                Article
                42501
                10.1038/s41467-023-42501-1
                10636102
                37945573
                e7b8cfcf-82d7-4fcd-9d96-6df2204e4a17
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 July 2023
                : 12 October 2023
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                © Springer Nature Limited 2023

                Uncategorized
                diagnostic markers,magnetic resonance imaging,machine learning
                Uncategorized
                diagnostic markers, magnetic resonance imaging, machine learning

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