Jorieke M Deschrevel, Anke A Andries, Karen Maes, Nathalie M De Beukelaer, Marlies Corvelyn, Lauraine M Staut, Hannah De Houwer, Domiziana Costamagna, Willem-Jan Metsemakers, Stefaan Nijs, Elga Nijs, Greet Hens, Kaat Desloovere, Anja Van Campenhout, Ghislaine Gayan-Ramirez
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This study aimed at defining the histological characteristics of the ST muscle in very young (preschool age group: 3-5 years old) and young (school age group: 6-9 years old) ambulant children with CP, in comparison to age-matched typically developing (TD) children. Microbiopsies of ST were collected in 37 children with CP and 33 TD children (preschool: 15 CP, 9 TD; school age: 22 CP, 24 TD). Muscle cross-sections were immunostained with (1) myosin heavy chain (MHC-I, MHC-IIa, and MHC-IIx) to determine fiber cross-sectional area (absolute: afCSA and normalized to total lower leg length: nfCSA), fiber proportion, (2) CD31 combined with MHC to assess capillary density, capillary to fiber ratio, capillary domain, and heterogeneity index, and (3) Pax7 to quantify the number of satellite cells. fCSA intrasubject variation was determined by coefficient of variation (CV). None of the parameters were altered in the preschool age CP compared to TD, except for larger type I afCSA in girls compared to boys. For the school-age group, type IIx afCSA (+21%, p = 0.019), nfCSA of all fibers (+48%, p = 0.03), and type IIa (+32%, p = 0.019) were larger in CP, and type IIx proportion was higher (+91%, p = 0.016) compared to TD. There was also an increased CV (all fibers: +30%, p = 0.005; type I: +32%, p < 0.001; IIa: +38%, p = 0.025). Satellite cell number and capillarization remained unaltered. 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Despite its relevant function in walking, the semitendinosus (ST) structure has been poorly investigated in CP, especially in (very) young children, although this could help determine early events and whether these alterations differ between age groups. This study aimed at defining the histological characteristics of the ST muscle in very young (preschool age group: 3-5 years old) and young (school age group: 6-9 years old) ambulant children with CP, in comparison to age-matched typically developing (TD) children. Microbiopsies of ST were collected in 37 children with CP and 33 TD children (preschool: 15 CP, 9 TD; school age: 22 CP, 24 TD). Muscle cross-sections were immunostained with (1) myosin heavy chain (MHC-I, MHC-IIa, and MHC-IIx) to determine fiber cross-sectional area (absolute: afCSA and normalized to total lower leg length: nfCSA), fiber proportion, (2) CD31 combined with MHC to assess capillary density, capillary to fiber ratio, capillary domain, and heterogeneity index, and (3) Pax7 to quantify the number of satellite cells. fCSA intrasubject variation was determined by coefficient of variation (CV). None of the parameters were altered in the preschool age CP compared to TD, except for larger type I afCSA in girls compared to boys. For the school-age group, type IIx afCSA (+21%, p = 0.019), nfCSA of all fibers (+48%, p = 0.03), and type IIa (+32%, p = 0.019) were larger in CP, and type IIx proportion was higher (+91%, p = 0.016) compared to TD. There was also an increased CV (all fibers: +30%, p = 0.005; type I: +32%, p < 0.001; IIa: +38%, p = 0.025). 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引用次数: 0
摘要
脑瘫(CP)是一种神经系统疾病,由发育中的胎儿或婴儿大脑非进行性病变引起,并伴有结构性肌肉改变。尽管半腱肌(ST)结构在行走中具有相关功能,但对CP的研究很少,特别是在(非常)年幼的儿童中,尽管这可以帮助确定早期事件以及这些改变是否在年龄组之间存在差异。本研究旨在确定非常年幼(学龄前:3-5岁)和年幼(学龄期:6-9岁)CP患儿的ST肌组织学特征,并与年龄匹配的典型发育(TD)患儿进行比较。对37例CP患儿和33例TD患儿(学龄前:15例CP, 9例TD;学龄:22例CP, 24例TD)进行ST活检。肌肉横断面采用(1)肌球蛋白重链(MHC- i、MHC- iia和MHC- iix)免疫染色测定纤维横截面面积(绝对:afCSA,归一化至小腿总长度:nfCSA)、纤维比例;(2)CD31联合MHC评估毛细密度、毛细与纤维比、毛细结构域和异质性指数;(3)Pax7定量测定卫星细胞数量。fCSA受试者内变异由变异系数(CV)确定。除了女孩的I型afCSA比男孩大外,学龄前CP的参数与TD相比都没有改变。学龄组中,IIx型afCSA (+21%, p = 0.019)、全纤维nfCSA (+48%, p = 0.03)和IIa型(+32%,p = 0.019)的CP较大,且IIx型比例高于TD (+91%, p = 0.016)。CV也增加(所有纤维:+30%,p = 0.005; I型:+32%,p = 0.005)
Histological analysis of the semitendinosus muscle in young children with cerebral palsy compared to age matched typically developing children.
Cerebral palsy (CP) is a neurological disorder caused by a non-progressive lesion in the developing fetal or infant brain associated with structural muscle alterations. Despite its relevant function in walking, the semitendinosus (ST) structure has been poorly investigated in CP, especially in (very) young children, although this could help determine early events and whether these alterations differ between age groups. This study aimed at defining the histological characteristics of the ST muscle in very young (preschool age group: 3-5 years old) and young (school age group: 6-9 years old) ambulant children with CP, in comparison to age-matched typically developing (TD) children. Microbiopsies of ST were collected in 37 children with CP and 33 TD children (preschool: 15 CP, 9 TD; school age: 22 CP, 24 TD). Muscle cross-sections were immunostained with (1) myosin heavy chain (MHC-I, MHC-IIa, and MHC-IIx) to determine fiber cross-sectional area (absolute: afCSA and normalized to total lower leg length: nfCSA), fiber proportion, (2) CD31 combined with MHC to assess capillary density, capillary to fiber ratio, capillary domain, and heterogeneity index, and (3) Pax7 to quantify the number of satellite cells. fCSA intrasubject variation was determined by coefficient of variation (CV). None of the parameters were altered in the preschool age CP compared to TD, except for larger type I afCSA in girls compared to boys. For the school-age group, type IIx afCSA (+21%, p = 0.019), nfCSA of all fibers (+48%, p = 0.03), and type IIa (+32%, p = 0.019) were larger in CP, and type IIx proportion was higher (+91%, p = 0.016) compared to TD. There was also an increased CV (all fibers: +30%, p = 0.005; type I: +32%, p < 0.001; IIa: +38%, p = 0.025). Satellite cell number and capillarization remained unaltered. These results indicate that the ST appears unaffected in very young ambulant CP children, but alterations develop with age.
期刊介绍:
Journal of Anatomy is an international peer-reviewed journal sponsored by the Anatomical Society. The journal publishes original papers, invited review articles and book reviews. Its main focus is to understand anatomy through an analysis of structure, function, development and evolution. Priority will be given to studies of that clearly articulate their relevance to the anatomical community. Focal areas include: experimental studies, contributions based on molecular and cell biology and on the application of modern imaging techniques and papers with novel methods or synthetic perspective on an anatomical system.
Studies that are essentially descriptive anatomy are appropriate only if they communicate clearly a broader functional or evolutionary significance. You must clearly state the broader implications of your work in the abstract.
We particularly welcome submissions in the following areas:
Cell biology and tissue architecture
Comparative functional morphology
Developmental biology
Evolutionary developmental biology
Evolutionary morphology
Functional human anatomy
Integrative vertebrate paleontology
Methodological innovations in anatomical research
Musculoskeletal system
Neuroanatomy and neurodegeneration
Significant advances in anatomical education.