Aim. The aim of the present work is to examine and compare brain abnormalities found on magnetic resonance imaging (MRI) in children diagnosed with autism spectrum disorders (ASD) and in children without this diagnosis. In terms of psychopathology, the aim is to evaluate a possible relationship between the MRI findings and the severity of autistic symptomatology. Methods. The research study is based on a retrospective analysis of a sample of patients who attended a diagnostic examination focused on ASD and at the same time underwent brain MRI at the Department of Child Psychiatry of the Second Faculty of Medicine at Charles University and University Hospital Motol between the years 1998 and 2015. For clinical diagnosis of ASD, the International Classification of Diseases, 10th revision (ICD-10), was used. Between 1998 and 1999, the assessment of patients was supported by the Childhood Autism Rating Scale. Starting in 2000, the third version of the Autism Diagnostic Interview - Revised was used for assessments; and from 2012 onwards, the Autism Diagnostic Observation Schedule - Generic was added to the diagnostic procedures. From 1998 to 2015, a total of 489 children were diagnosed with pervasive developmental disorder (404 boys, 85 girls). The mean age in the group was 8.0 ± 4.2 years (range...

京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第19554号 / 医博第4061号 / 新制||医||1012(附属図書館) / 32590 / 京都大学大学院医学研究科医学専攻 / (主査)教授 伊佐 正, 教授 渡邉 大, 教授 髙橋 良輔 / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM

京都大学 / 0048 / 新制・課程博士 / 博士(医学) / 甲第19889号 / 医博第4138号 / 新制||医||1016(附属図書館) / 32966 / 京都大学大学院医学研究科医学専攻 / (主査)教授 古川 壽亮, 教授 髙橋 良輔, 教授 富樫 かおり / 学位規則第4条第1項該当 / Doctor of Medical Science / Kyoto University / DFAM

No description available.

No description available.

Children with unilateral spastic cerebral palsy (USCP) have impairments affecting upper limb function, particularly in grasping abilities. Specifically, children with USCP may display precision grip impairments, which can lead to activity limitations. The interplay between feedforward and feedback control is essential for successful grasping, requiring somatosensory information to be integrated with the motor output. This integration occurs through the transmission of somatosensory information through the dorsal column medial lemniscus (DCML) pathway, while independent finger movement to grasp an object is controlled by the motor cortex via the corticospinal tract (CST). While previous studies demonstrated the CST relates to anticipatory control of grasping, this may not explain all the variance of grasp impairments in children with USCP. Although studies have highlighted the importance of sensory information in grasping in typically developing (TD) adults, there are no studies examining the relationship between brain structure and function in terms of precision grip impairments in children with USCP. Additionally, sensorimotor integration plays an important role in precision grip. In some children with USCP, the lesion that occurs in the brain can cause the CST to reorganize to the contralesional hemisphere. This results in the sensory and motor tracts in different hemispheres, impacting motor impairments. When this sensory-motor dissociation occurs or when there are successive lifts of an object with each hand, it is thought that the information is transferred through the corpus callosum (CC). However, damage to the CC can restrict somatosensory processing, which can further impair grasping abilities. Previous studies have only looked at precision grip impairments in relation to the CST. Therefore, an integrative approach is necessary to fully understand the mechanisms of precision grip impairments in children with USCP. In this study our aim was to examine the neural basis of precision grip in children with USCP. Twenty-seven children participated in an MRI assessment. This included the acquisition of structural and diffusion-weighted images (DWI) to extract diffusion metrics of the CST, DCML pathway, and CC. Children also participated in clinical sensory measures, including the stereognosis test, grating orientation task, and the two-point discrimination task. Additionally, children performed precision grip lifts using a custom-made object. All children were asked to grasp an object with interchangeable surfaces (i.e., sandpaper and rayon) to measure adaptation of grip force (GF) to object texture. They were also asked to grasp the same object, hold it in the air and slowly release their grip so that the object gradually slips from their fingertips. Twenty-seven children performed these tasks with their less affected hand, and 16 with their more affected hand. Additionally, 17 participants grasped an object with various weights with each lifting sequence consisting of lifting an object in succession with the same hand and then one lift with the contralateral hand. The results demonstrate the greater reduction of integrity (more damage) of the DCML pathway, the poorer the grasp task performance, as indicated through the safety margin (the difference between the minimum amount of force needed to prevent slipping and the applied grip force). Regression analyses and cluster analyses display that CST integrity and organization may also contribute to safety margin. This suggests that diffusion metrics of multiple pathways and CST organization when considered together contribute to grasping impairments in children with USCP. To assess this further, we examined the relative difference in the peak rate of force between objects with various weights during successive lifts with each hand. Children with USCP did demonstrate anticipatory control within hands and a generalization of anticipatory control between hands. However, a loss of the transfer information was shown when first grasping the object with their less affected hand and then their more affected hand, in children with an absent contralateral CST. Therefore, the results suggest precision grip impairments may not exclusively be due to sensory impairments, but instead how the sensory information is integrated with the motor output of the same hand.

This thesis describes the developmental expression and anatomical distribution of Copine-6, a neuron specific member of the Copine family of calcium-dependent phospholipid-binding proteins, in rodent brain. A polyclonal antibody targeting the full Copine-6 sequence has been characterised prior to its employment for the immunohistochemical analysis of rodent embryonic and adult brain tissue. Several different Copine-6 labelled neuron populations in the neocortex, hippocampus and olfactory bulbs were discovered, and one of these with an unusual ‘spiny’ morphology in the adult rodent corpus callosum, bordering the neurogenic subventricular zone and rostral migratory stream, was studied in detail. A full molecular characterisation of these Copine-6 ‘spiny’ neurons showed that these cells are mature, GABAergic, axonless interneurons with putative synaptic communication, unusual for their location in the white matter close to the region of adult neurogenesis. A full bromodeoxyuridine (BrdU) birth-dating analysis was performed, which indicated an early embryonic birthdate for the Copine-6 spiny cells. This timeframe is typical of cortical GABAergic interneurons suggesting that their unusual positioning is programmed from embryogenesis. Furthermore, electron microscopic analysis of these Copine-6 interneurons in Chapter 5 confirms that indeed these cells contain vesicles and are synaptically integrated as postsynaptic recipients. The presence of vesicles in the architecturally dendritic processes is suggestive of dendro-dendritic signalling by these cells. Observations from electron microscopic nanoparticle labelling also showed that the Copine-6 protein is restricted to the plasma membrane, smooth endoplasmic reticulum, and multi-vesicular bodies. These embryonically generated Copine-6 labelled axonless interneurons are a novel neuron population in the corpus callosum, and the presence of vesicles in the dendritic processes of these cells suggests that they might have a novel communication mechanism.

O corpo caloso é a maior comissura cerebral, responsável pela conexão entre os hemisférios cerebrais. Anatomicamente está localizado na profundidade da fissura inter-hemisférica e é dividido em quatro regiões: esplênio, corpo, joelho e rostro, que se continua inferiormente na lamina rostralis. A malformação do corpo caloso (MCC) representa uma desorganização na arquitetura cerebral, resultante da impossibilidade parcial ou completa das fibras da comissura calosa atravessarem a linha média. Pode estar associada a outras malformações, tanto do sistema nervoso central quanto de outros órgãos. As causas de malformações do corpo caloso são múltiplas, podendo ser ambientais, vasculares ou genéticas. As malformações do corpo caloso são comuns, principalmente entre as crianças com distúrbio do desenvolvimento neuropsicomotor ou retardo mental, mas podem também ser observada em indivíduos normais. Existem mais de 50 síndromes clínicas, autossômicas ou ligadas ao X, dominantes ou recessivas, associadas a MCC. A investigação de pacientes com malformação de corpo caloso por meio do cariótipo com bandas G identificou cerca de 20 regiões cromossômicas associadas a esta malformação. Nos últimos anos, novas técnicas de investigação cromossômica com alta resolução tornam-se disponíveis, como a hibridação comparativa do genoma em microarranjos (CGH-array). O CGH-array permite uma análise rápida de todo o genoma em alta resolução, possibilitando reconhecer variações no número de cópias de regiões genômicas com de 0,1 a 1 Mb, e desta forma detectar microdeleções ou microduplicações que não são passiveis de serem reconhecidas pelo cariótipo com bandas G, que é capaz de detectar alterações com no mínimo 4 Mb. Nesta investigação foram incluídos 21 sujeitos com MCC, associada ou não a outras malformações encefálicas ou de outros órgãos, e atraso do desenvolvimento neuropsicomotor ou retardo mental, sem etiologia definida. Estes sujeitos foram investigados com o objetivo de detectar anormalidades cromossômicas, estruturais e/ou numéricas, por meio do cariótipo com bandas G, e de variações do número de cópias de regiões genômicas, por meio do estudo com CGH-array. O cariótipo evidenciou alteração em dois dos sujeitos (9.5%): um indivíduo apresentava um derivado do cromossomo 4 [46, XX, der(4)] herdado da mãe, que apresentava translocação balanceada entre os cromossomos 4 e 10 [46, XX,t(4; 10)(q35; q23)]; e outro apresentava um rearranjo de novo, derivado do cromossomo 8, [46, XX, der(8)]. O CGH-array foi feito nestes indivíduos para delimitar a extensão e a origem do material genético presente no rearranjo. Em dois indivíduos (11%), o CGH-array evidenciou alterações cromossômicas de novo: deleção em 6q25.1-25.3, com dimensão entre 5 e 6,7 Mb, e deleção 4q25-q28.1 com 14,5 Mb. E finalmente, em quatro sujeitos (21%), o CGH-array detectou variação no número de cópias genômicas, evidente também em um dos genitores, com significado clínico incerto. Desta forma, a investigação de alterações cromossômicas nesta amostra de 21 pacientes com MCC, permitiu: (1). Diagnosticar, com o auxílio do cariótipo, anormalidades estruturais cromossômicas em dois casos; (2). Diagnosticar, com o auxílio do CGH-array, microdeleções não visualizáveis ao cariótipo em dois pacientes; (3). Caracterizar, com o auxílio do CGH-array, a extensão e origem dos rearranjos diagnosticados pelo cariótipo. A existência de translocação equilibrada em genitor de um dos pacientes com cariótipo anormal aumenta o risco de recorrência, de anormalidades, em outras gestações. Nos demais três pacientes, este risco é considerado muito baixo. Duas das alterações cromossômicas encontradas em nossos pacientes, a deleção na região 6q25.1-25.3 e a duplicação invertida no cromossomo 8 na região p23.1 - p11.21, já foram previamente descritas em MCC. Porém não há descrições envolvendo a deleção 4q25-q28 ou a deleção 4q34.3-q35.2 combinada com a duplicação 10q 23.1 - q23.6. A investigação de alterações cromossômicas em indivíduos com MCC contribui para o esclarecimento de sua etiologia e auxilia no delineamento de regiões cromossômicas que contém genes envolvidos com a formação do corpo caloso / The corpus callosum is the largest cerebral commissure and is responsible for interconnection of cerebral hemispheres. It is located in the deepest part of the interhemispheral fissure and is divided in four regions: splenium, body, genum and rostrum, which is prolonged inferiorly as lamina rostralis. Corpus callosum malformation (CCM) is a cerebral architecture disorganization caused by complete or partial failure of callosum fibers to cross the midline. It may be associated to other malformations, both from central nervous system and other organs. Many factors can contribute do CCM, including environmental, vascular and genetics. CCM are particularly common among mentally retarded or developmentally delayed children but can also be observed in cognitively normal individuals. There are more than 50 clinical syndromes associated to CCM, occurring sporadically or inherited as an autosomal or X-linked, dominant or recessive trait. Karyotype with G-banding disclosed around to 20 chromosomal regions associated to CCM. In the last few years, new techniques for high resolution chromosomal investigation, as comparative genomic hybridization array (CGH-array), became available. CGH-array allows fast analysis in high resolution of the genome, allowing the determination of copy number variations (microduplications and microdeletions) of genomic regions, with minimum size of 0, 1 to 1 Mb. This resolution is much larger than of the conventional karyotype, which is able to detect abnormalities of at least 4 Mb. This investigation included 21 subjects with CCM without defined etiology, associated or not to additional brain or other internal organ malformation and with developmental delay or mental retardation. These individuals were investigated for numeric or structural chromosomal abnormalities with karyotype with G-banding and for genomic copy number variations, using CGH-array. Karyotype disclosed abnormalities in two individuals (9.5%): one patient had a derived chromosome 4 [46, XX,der(4)], inherited from his mother, which has a balanced translocation between chromosomes 4 and 10 [46,XX,t(4;10)(q35;q23)]; and other had a de novo rearrangement, derived from chromosome 8 [46, XX,der(8)]. CGHarray analysis was conducted in these individuals to define the extension and origin of the genetic material present in the rearrangement. Among individuals with normal karyotype, CGH-array disclosed two patients (11%), with de novo abnormalities: 6q25.1-25.3 deletion, with size ranging from 5 to 6, 7 Mb, and a 14.5 deletion of 4q25-q28.1. Finally, in four subjects (21%), CGH-array detected genomic copy number variations that were also present in one of the parents, which make its clinical significance uncertain. To conclude, the investigation of chromosomal abnormalities in this sample of 21 patients with CCM, allow us to: 1. Detect two patients with chromosomal abnormalities detectable on conventional karyotype; 2. Recognize, with CGH-array technique, two additional patients with microdeletions, not seen on conventional karyotype; 3. Characterize the origin and extension of chromosomal rearrangement in the patients with abnormal karyotype. The detection of a balanced translocation in one of the parents increases the risk of occurrence of chromosomal abnormalities in future concepts of this individual. In the remaining three patients, recurrence risk is presumably very low. Two of the chromosomal abnormalities detected in our patients (6q25.1- 25.3 deletion and inverted duplication of chromosome 8 spanning p23.1 - p11.21) have been previously reported in patients with CCM. Nevertheless, chromosomal abnormalities involving chromosome 4 (deletion 4q25-q28.1) or the combined deletion 4q34.3 - q35.2 and duplication 10q 23.1 - q23.6 have not been previously reported. Investigation of chromosomal abnormalities in individuals with CCM contributes to etiology determination and helps delineation of chromosomal regions that contains gene(s) involved with corpus callosum formation.

Introdução: O acesso ao terceiro ventrículo constitui verdadeiro desafio ao neurocirurgião. Nesse contexto, estudos anatômicos e morfométricos são úteis para estabelecer as limitações e as vantagens de determinado acesso cirúrgico. O acesso transcorioideo é versátil e promove exposição adequada da região média e posterior do terceiro ventrículo. Entretanto, a coluna do fórnice limita a exposição da região anterior do terceiro ventrículo. Há evidências de que a secção ipsilateral da coluna do fórnice tenha pouca repercussão na função cognitiva. Esta tese compara a exposição anatômica proporcionada pelo acesso transforniceal transcorioideo com o do acesso transcorioideo e realiza avaliação morfométrica de estruturas relevantes e comuns aos dois acessos. Material e métodos: A exposição anatômica proporcionada pelos acessos transcaloso transcorioideo e transcaloso transforniceal transcorioideo foram comparadas em oito cadáveres não submetidos à conservação, utilizando o sistema de neuronavegação (Artis, Brasília, Brasil), para aferir a área de trabalho, a área de exposição microcirúrgica, a exposição angular no plano longitudinal e transversal de dois alvos anatômicos (túber cinéreo e aqueduto cerebral). Adicionalmente, foram quantificados a espessura do parênquima do lobo frontal direito, a espessura do tronco do corpo caloso, o diâmetro longitudinal do forame interventricular, a distância de trabalho da superfície cortical ao túber cinéreo e a distância de trabalho da superfície cortical até o aqueduto cerebral. Os valores obtidos foram submetidos a análise de estatística utilizando o teste de Wilcoxon. Resultados: Na avaliação quantitativa, o acesso transforniceal transcorioideo proporcionou maior área de trabalho (transforniceal transcorioideo = 150,299 +/- 11,147 mm2; transcorioideo = 121,421 +/- 7,698 mm2; p < 0,05), maior área de exposição microcirúrgica (transforniceal transcorioideo = 100,920 +/- 8,764 mm2; transcorioideo = 79,944 +/- 4,954 mm2; p < 0,05), maior área de exposição angular no plano longitudinal para o túber cinéreo (transforniceal transcorioideo = 70,898 +/- 6,598 graus; transcorioideo = 63,838 +/- 5,770 graus; p < 0,05) e maior área de exposição angular no plano longitudinal para o aqueduto cerebral (transforniceal transcorioideo = 61,806 +/- 6,406 graus; transcorioideo = 54,998 +/- 5,102 graus; p < 0,05) em comparação com o acesso transcorioideo. Nenhuma diferença foi observada na exposição angular ao longo do eixo transversal para os dois alvos anatômicos (túber cinéreo e aqueduto cerebral) (p > 0,05). A espessura média do lobo frontal direito foi de 34,869 +/- 3,439 mm, a espessura do tronco caloso foi 10,085 +/- 1,172 mm, o diâmetro do forame interventricular foi de 4,628 +/- 0,474 mm, a distância da superfície cortical ao túber cinéreo foi de 69,315 +/- 4,564 mm e a distância da superfície cortical ao aqueduto cerebral foi de 75,654 +/- 4,950 mm. Na avaliação qualitativa, observamos que o acesso transforniceal transcorioideo permitiu incremento da visualização das estruturas da região anteroinferior do terceiro ventrículo. Não houve diferença quanto à exposição das estruturas da região média e posterior em ambos os acessos. Conclusões: O acesso transforniceal transcorioideo propicia maior exposição cirúrgica da região anterior do terceiro ventrículo em comparação com aquela oferecida pelo acesso transcorioideo. O estudo morfométrico estabeleceu valores médios das estruturas anatômicas comuns aos dois acessos na população estudada / Introduction: Approaches to the third ventricle constitute a formidable challenge to the neurosurgeon and, in this context, anatomical and morphometric studies are useful to establish the limitations and advantages of certain surgical approaches. The transchoroidal approach is a versatile one that promotes adequate exposure of the middle and posterior regions of the third ventricle. However, the column of fornix limits the exposure of the anterior third ventricle region. There is evidence that the ipsilateral section of the column of fornix has little effect on the cognitive function. This thesis compares the anatomical exposure using the transchoroidal transforniceal technique with the transchoroidal approach, and performs morphometric assessment of relevant structures common to both approaches. Material and methods: The anatomical exposure achieved through the transchoroidal transcallosal approach and transchoroidal transforniceal transcallosal were compared in 8 fresh cadavers using the neuronavigation system (Artis, Brasilia, Brazil), to assess the working area, microsurgical exposure area, to quantify the angular exposure in the longitudinal and cross-sectional planes to two anatomical targets (tuber cinereum and cerebral aqueduct), to measure the thickness of the right frontal lobe parenchyma, corpus callosum body thickness, longitudinal diameter of the interventricular foramen, working distance from the cortical surface to the tuber cinereum and working distance from the cortical surface to the cerebral aqueduct. The values obtained were submitted to statistical analysis using Wilcoxon\'s test. Results: In the quantitative assessment, the transchoroidal transforniceal approach provided: larger working area (transchoroidal transforniceal = 150.299 +/- 11.147 mm2; transchoroidal = 121.421 +/- 7.698 mm2; p < 0.05), larger area of microsurgical exposure (transforniceal transchoroidal = 100.920 +/- 8.764 mm2; transchoroidal = 79.944 +/- 4.954 mm2; p < 0.05), larger area of angular exposure in the longitudinal plane to the tuber cinereum (transchoroidal transforniceal = 70.898 +/- 6.598 degrees; transchoroidal = 63.838 + / - 5,770 degrees; p < 0.05) and larger area of angular exposure in the longitudinal plane to the cerebral aqueduct (transforniceal transchoroidal = 61.806 +/- 6.406 degrees; transchoroidal = 54.998 +/- 5.102 degrees; p < 0.05) when compared to the transchoroidal approach. No differences were observed in the angular exposure along the cross-sectional axis for both anatomical targets (tuber cinereum and cerebral aqueduct) (p > 0.05). The mean thickness of the right frontal lobe was 34.869 +/- 3.439 mm, the thickness of the corpus callosum body was 10.085 +/- 1.172 mm, the diameter of the interventricular foramen was 4,628 +/- 0,474 mm, the distance from the cortical surface to the tuber cinereum was 69.315 +/- 4.564 mm, and the distance from the cortical surface to the cerebral aqueduct was 75.654 +/- 4.950 mm. In the qualitative assessment, we observed that the transforniceal transchoroidal approach allowed better visualization of the structures in the anterior third ventricle region. There was no difference regarding exposure of structures in the middle and posterior regions with both access. Conclusions: The transforniceal transchoroidal approach provides greater surgical exposure of the anterior third ventricle region than that obtained with the transchoroidal approach. The morphometric study established mean values of anatomical structures that are common to both approaches in the assessed population

A exposição a eventos traumáticos durante a infância está associada a um prejuízo na cognição, neurobiologia e morfologia cerebral. No entanto, não se sabe se o trauma está relacionado a essas mudanças em amostras que não apresentam potenciais fatores de confusão como idade avançada, cronicidade do transtorno psiquiátrico e múltiplos episódios de humor. O impacto do trauma na infância foi avaliado em duas amostras diferentes nesta tese: 1) crianças com e sem história de trauma; 2) pacientes com diagnóstico de THB logo após a recuperação do primeiro episódio de mania com e sem história de trauma na infância e controles saudáveis com e sem história de trauma na infância. Os resultados sugerem que o trauma está associado a mudanças na neurobiologia, cognição e morfologia cerebral. Crianças com trauma apresentaram aumento nos níveis de BDNF, TNF-α, IL-6 e IL-10 comparadas com crianças sem trauma. No entanto, após a exclusão de crianças com história de doença inflamatória, apenas os níveis de BDNF e TNF-α permaneceram aumentados em crianças com trauma. Na população com transtorno bipolar, a história de trauma na infância foi associada a uma diminuição no QI, atenção auditiva e memória verbal e memória de trabalho enquanto um padrão diferente foi observado nos controles saudáveis com história de abuso infantil. Pacientes com THB e trauma também apresentaram menor volume total do CC em comparação aos pacientes com THB e sem trauma, com diferenças significativas também na região anterior do CC. Por outro lado, não encontramos diferenças significativas entre o volume do CC nos pacientes com ou sem trauma em comparação aos controles saudáveis. Estes achados reforçam a extensão e gravidade do impacto negativo do trauma na infância, em diferentes etapas do desenvolvimento, afetando tanto aspectos cognitivos, como neurobiológicos e de morfologia cerebral. / Exposure to traumatic events during childhood is associated with impairment in cognition, neurobiology and brain morphology. However, it is unknown if trauma is related to these changes in samples that do not show the potential confounds of advancing age, chronicity of psychiatry disorder and multiple mood episodes. We evaluated the impact of childhood trauma in two different samples: 1) children with and without childhood trauma; 2) pacients with a BD diagnosis recently recovered from a first manic episode with and without childhood trauma and healthy controls with and without childhood trauma. The results suggest that childhood trauma is associated to changes in neurobiology, cognition and brain morphology. Children with trauma showed higher levels of BDNF, TNF-α, IL-6 e IL-10 compared to children without trauma. However, after excluding children with history of inflammatory disease, only BDNF and TNF-α levels remained increased in children with trauma. In BD patients, the childhood trauma was associated to a decreased IQ, auditory attention, verbal memory, and working memory and a different pattern was observed in healthy subjects with a history of childhood abuse. The total CC volume was found to be smaller in BD patients with trauma compared to BD patients without trauma and differences were more pronounced also in the anterior region of the CC. On the other hand, we did not find significant differences in the CC volume of patients with/without trauma compared to the healthy subjects. These findings reinforce the extent and severity of the negative impact of childhood trauma in different stages of development, affecting cognitive aspects, as well as neurobiological and brain morphology.