Elizabeth A. Hodgdon , Ryan Anderson , Hussein Al Azzawi , Tony W. Wilson , Vince D. Calhoun , Yu-Ping Wang , Isabel Solis , Douglas N. Greve , Julia M. Stephen , Kristina T.R. Ciesielski
{"title":"小脑前部和后部蚓部的磁共振成像形态计量及其与儿童感觉运动和认知功能的关系","authors":"Elizabeth A. Hodgdon , Ryan Anderson , Hussein Al Azzawi , Tony W. Wilson , Vince D. Calhoun , Yu-Ping Wang , Isabel Solis , Douglas N. Greve , Julia M. Stephen , Kristina T.R. Ciesielski","doi":"10.1016/j.dcn.2024.101385","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>The human cerebellum emerges as a posterior brain structure integrating neural networks for sensorimotor, cognitive, and emotional processing across the lifespan. Developmental studies of the cerebellar anatomy and function are scant. We examine age-dependent MRI morphometry of the <em>anterior cerebellar vermis</em>, lobules I-V and <em>posterior neocortical lobules</em> VI-VII and their relationship to sensorimotor and cognitive functions.</p></div><div><h3>Methods</h3><p>Typically developing children (TDC; n=38; age 9–15) and healthy adults (HAC; n=31; 18–40) participated in high-resolution MRI. Rigorous anatomically informed morphometry of the vermis lobules I-V and VI-VII and total brain volume (TBV) employed manual segmentation computer-assisted FreeSurfer Image Analysis Program [<span>http://surfer.nmr.mgh.harvard.edu</span><svg><path></path></svg>]. The neuropsychological scores (WASI-II) were normalized and related to volumes of anterior, posterior vermis, and TBV.</p></div><div><h3>Results</h3><p>TBVs were age independent. Volumes of I-V and VI-VII were significantly reduced in TDC. The ratio of VI-VII to I-V (∼60%) was stable across age-groups; I-V correlated with visual-spatial-motor skills; VI-VII with verbal, visual-abstract and FSIQ.</p></div><div><h3>Conclusions</h3><p>In TDC neither anterior I-V nor posterior VI-VII vermis attained adult volumes. The <em>\"inverted U\"</em> developmental trajectory of gray matter peaking in adolescence does not explain this finding. The hypothesis of protracted development of oligodendrocyte/myelination is suggested as a contributor to TDC's lower cerebellar vermis volumes.</p></div>","PeriodicalId":49083,"journal":{"name":"Developmental Cognitive Neuroscience","volume":"67 ","pages":"Article 101385"},"PeriodicalIF":4.6000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S187892932400046X/pdfft?md5=9357f0a9eb74d438fdcb73bfc966bf81&pid=1-s2.0-S187892932400046X-main.pdf","citationCount":"0","resultStr":"{\"title\":\"MRI morphometry of the anterior and posterior cerebellar vermis and its relationship to sensorimotor and cognitive functions in children\",\"authors\":\"Elizabeth A. Hodgdon , Ryan Anderson , Hussein Al Azzawi , Tony W. Wilson , Vince D. Calhoun , Yu-Ping Wang , Isabel Solis , Douglas N. Greve , Julia M. Stephen , Kristina T.R. Ciesielski\",\"doi\":\"10.1016/j.dcn.2024.101385\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>The human cerebellum emerges as a posterior brain structure integrating neural networks for sensorimotor, cognitive, and emotional processing across the lifespan. Developmental studies of the cerebellar anatomy and function are scant. We examine age-dependent MRI morphometry of the <em>anterior cerebellar vermis</em>, lobules I-V and <em>posterior neocortical lobules</em> VI-VII and their relationship to sensorimotor and cognitive functions.</p></div><div><h3>Methods</h3><p>Typically developing children (TDC; n=38; age 9–15) and healthy adults (HAC; n=31; 18–40) participated in high-resolution MRI. Rigorous anatomically informed morphometry of the vermis lobules I-V and VI-VII and total brain volume (TBV) employed manual segmentation computer-assisted FreeSurfer Image Analysis Program [<span>http://surfer.nmr.mgh.harvard.edu</span><svg><path></path></svg>]. The neuropsychological scores (WASI-II) were normalized and related to volumes of anterior, posterior vermis, and TBV.</p></div><div><h3>Results</h3><p>TBVs were age independent. Volumes of I-V and VI-VII were significantly reduced in TDC. The ratio of VI-VII to I-V (∼60%) was stable across age-groups; I-V correlated with visual-spatial-motor skills; VI-VII with verbal, visual-abstract and FSIQ.</p></div><div><h3>Conclusions</h3><p>In TDC neither anterior I-V nor posterior VI-VII vermis attained adult volumes. The <em>\\\"inverted U\\\"</em> developmental trajectory of gray matter peaking in adolescence does not explain this finding. The hypothesis of protracted development of oligodendrocyte/myelination is suggested as a contributor to TDC's lower cerebellar vermis volumes.</p></div>\",\"PeriodicalId\":49083,\"journal\":{\"name\":\"Developmental Cognitive Neuroscience\",\"volume\":\"67 \",\"pages\":\"Article 101385\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S187892932400046X/pdfft?md5=9357f0a9eb74d438fdcb73bfc966bf81&pid=1-s2.0-S187892932400046X-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental Cognitive Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S187892932400046X\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Cognitive Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S187892932400046X","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
导言人类的小脑是一种后脑结构,它整合了整个生命周期中感觉运动、认知和情感处理的神经网络。有关小脑解剖和功能的发育研究很少。我们研究了小脑前部蚓部、I-V小叶和后部新皮质VI-VII小叶随年龄变化的核磁共振成像形态测量,以及它们与感觉运动和认知功能的关系。采用人工分割计算机辅助FreeSurfer图像分析程序[http://surfer.nmr.mgh.harvard.edu],对蚓部小叶I-V和VI-VII及脑总体积(TBV)进行了严格的解剖形态测量。对神经心理学评分(WASI-II)进行了归一化处理,并将其与前蚓部、后蚓部和总脑容量相关联。在 TDC 中,I-V 和 VI-VII 的体积明显缩小。VI-VII与I-V的比率(∼60%)在各年龄组中保持稳定;I-V与视觉空间运动技能相关;VI-VII与言语、视觉抽象和FSIQ相关。灰质在青春期达到顶峰的 "倒 U 型 "发育轨迹并不能解释这一发现。少突胶质细胞/髓鞘化的长期发育假说被认为是导致TDC小脑蚓部体积较小的原因之一。
MRI morphometry of the anterior and posterior cerebellar vermis and its relationship to sensorimotor and cognitive functions in children
Introduction
The human cerebellum emerges as a posterior brain structure integrating neural networks for sensorimotor, cognitive, and emotional processing across the lifespan. Developmental studies of the cerebellar anatomy and function are scant. We examine age-dependent MRI morphometry of the anterior cerebellar vermis, lobules I-V and posterior neocortical lobules VI-VII and their relationship to sensorimotor and cognitive functions.
Methods
Typically developing children (TDC; n=38; age 9–15) and healthy adults (HAC; n=31; 18–40) participated in high-resolution MRI. Rigorous anatomically informed morphometry of the vermis lobules I-V and VI-VII and total brain volume (TBV) employed manual segmentation computer-assisted FreeSurfer Image Analysis Program [http://surfer.nmr.mgh.harvard.edu]. The neuropsychological scores (WASI-II) were normalized and related to volumes of anterior, posterior vermis, and TBV.
Results
TBVs were age independent. Volumes of I-V and VI-VII were significantly reduced in TDC. The ratio of VI-VII to I-V (∼60%) was stable across age-groups; I-V correlated with visual-spatial-motor skills; VI-VII with verbal, visual-abstract and FSIQ.
Conclusions
In TDC neither anterior I-V nor posterior VI-VII vermis attained adult volumes. The "inverted U" developmental trajectory of gray matter peaking in adolescence does not explain this finding. The hypothesis of protracted development of oligodendrocyte/myelination is suggested as a contributor to TDC's lower cerebellar vermis volumes.
期刊介绍:
The journal publishes theoretical and research papers on cognitive brain development, from infancy through childhood and adolescence and into adulthood. It covers neurocognitive development and neurocognitive processing in both typical and atypical development, including social and affective aspects. Appropriate methodologies for the journal include, but are not limited to, functional neuroimaging (fMRI and MEG), electrophysiology (EEG and ERP), NIRS and transcranial magnetic stimulation, as well as other basic neuroscience approaches using cellular and animal models that directly address cognitive brain development, patient studies, case studies, post-mortem studies and pharmacological studies.