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1.
Neuroradiology ; 66(9): 1553-1564, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-38886214

RESUMO

PURPOSE: To characterize Vanishing White Matter Disease (VWM) cases from a Brazilian University Tertiary hospital, focusing on brain magnetic resonance image (MRI) aspects, clinical and molecular data. METHODS: Medical records and brain MRI of 13 genetically confirmed VWM patients were reviewed. Epidemiological data such as age at symptom onset, gender and main symptoms were analyzed, along with genetic mutations and MRI characteristics, such as the distribution of white matter lesions and atrophy. RESULTS: The majority of patients were female, with the age of symptom onset ranging from 1 year and 6 months to 40 years. All mutations were identified in the EIF2B5 gene, the most prevalent being c.338G > A (p.Arg113His), and a novel mutation related to the disease was discovered, c.1051G > A (p.Gly351Ser). Trauma or infection were significant triggers. The most frequent symptoms were ataxia and limb spasticity. All MRI scans displayed deep white matter involvement, cystic degeneration, with U-fibers relatively spared and a predilection for the frontoparietal region. Lesions in the corpus callosum and posterior fossa were present in all patients. Follow-up exams revealed the evolution of white matter lesions and cerebral atrophy, which correlated with clinical deterioration. CONCLUSIONS: VWM affects various age groups, with a significant clinical and genetic variability. A novel mutation associated with the disease is highlighted. MRI reveals a typical pattern of white matter involvement, characterized by diffuse lesions in the periventricular and deep regions, with subsequent extension to the subcortical areas, accompanied by cystic degeneration, and plays a crucial role in diagnosis and follow-up.


Assuntos
Leucoencefalopatias , Imageamento por Ressonância Magnética , Humanos , Feminino , Masculino , Brasil , Adulto , Leucoencefalopatias/diagnóstico por imagem , Leucoencefalopatias/genética , Criança , Adolescente , Imageamento por Ressonância Magnética/métodos , Lactente , Pré-Escolar , Mutação , Adulto Jovem , Fator de Iniciação 2B em Eucariotos/genética
2.
Laryngoscope Investig Otolaryngol ; 9(1): e1195, 2024 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-38362200

RESUMO

Objectives: To investigate the use of a novel technique to estimate the symmetrical placement of percutaneous bone-anchored hearing systems (BAHS) with a guide-marker in patients undergoing bilateral surgery with this device. Study Design: Prospective cohort study. Methods: A guide-marker and anatomical landmarks were used to estimate the implant placement and transferred to the contralateral ear in 12 subjects eligible for bilateral BAHS surgery. To investigate the bilateral symmetry, preoperative tri-dimensional (3D) computed tomography (CT) image reconstruction was used to compare the distances between the mandibular condyle and implant placement estimation (mandible-implant distance) in both the right and left ears of the subjects. Results: The guide-marker could be used to estimate the bilateral implant placement in all subjects included in this study, simply and easily, including one subject with craniofacial malformation. The mean mandible-implant distances were 5.37 and 5.38 cm, in the right and left ears of the subjects, respectively, and no differences were observed between them, thereby indicating optimal bilateral symmetry. Conclusion: The use of the guide-marker proved to be an effective tool to provide symmetrical placement of bilateral BAHS. We propose a novel method employing a simple guide-marker and tracing based on symmetrical anatomical landmarks to achieve precise placement and optimal symmetry and which may be easily adopted in the surgical routine of BAHS. Level of Evidence: 3.

3.
Magn Reson Imaging ; 111: 217-228, 2024 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-38754751

RESUMO

Accurately studying structural connectivity requires precise tract segmentation strategies. The U-Net network has been widely recognized for its exceptional capacity in image segmentation tasks and provides remarkable results in large tract segmentation when high-quality diffusion-weighted imaging (DWI) data are used. However, short tracts, which are associated with various neurological diseases, pose specific challenges, particularly when high-quality DWI data acquisition within clinical settings is concerned. Here, we aimed to evaluate the U-Net network ability to segment short tracts by using DWI data acquired in different experimental conditions. To this end, we conducted three types of training experiments involving 350 healthy subjects and 11 white matter tracts, including the anterior, posterior, and hippocampal commissure, fornix, and uncinated fasciculus. In the first experiment, the model was exclusively trained with high-quality data of the Human Connectome Project (HCP) dataset. The second experiment focused on images of healthy subjects acquired from a local hospital dataset, representing a typical clinical routine acquisition. In the third experiment, a hybrid training approach was employed, combining data of the HCP and local hospital datasets. Then, the best model was also tested in unseen DWIs of 10 epilepsy patients of the local hospital and 10 healthy subjects acquired on a scanner from another company. The outcomes of the third experiment demonstrated a notable enhancement in performance when contrasted with the preceding trials. Specifically, the short tracts within the local hospital dataset achieved Dice scores ranging between 0.60 and 0.65. Similar intervals were obtained with HCP data in the first experiment, and a substantial improvement compared to the scores between 0.37 and 0.50 obtained with the local hospital dataset at the same experiment. This improvement persisted when the method was applied to diverse scenarios, including different scanner acquisitions and epilepsy patients. These results indicate that combining datasets from different sources, coupled with resolution standardization strengthens the neural network ability to generalize predictions across a spectrum of datasets. Nevertheless, short tract segmentation performance is intricately linked to the training composition, to validation, and to testing data. Moreover, curved tracts have intricate structural nature, which adds complexities to their segmenting. Although the network training approach tested herein has provided promising results, caution must be taken when extrapolating its application to datasets acquired under distinct experimental conditions, even in the case of higher-quality data or analysis of long or short tracts.


Assuntos
Conectoma , Epilepsia , Processamento de Imagem Assistida por Computador , Substância Branca , Humanos , Masculino , Feminino , Processamento de Imagem Assistida por Computador/métodos , Adulto , Epilepsia/diagnóstico por imagem , Substância Branca/diagnóstico por imagem , Imagem de Difusão por Ressonância Magnética/métodos , Encéfalo/diagnóstico por imagem , Imagem de Tensor de Difusão/métodos , Imageamento por Ressonância Magnética/métodos , Algoritmos
4.
Artigo em Inglês | MEDLINE | ID: mdl-38181427

RESUMO

INTRODUCTION: Studies addressing the methylation pattern in adamantinomatous craniopharyngioma (ACP) are lacking. OBJECTIVE: To identify methylation signatures in ACPs regarding clinical presentation and outcome. METHODS: Clinical and pathology data were collected from 35 ACP patients (54% male; 18.1 years [2-68]). CTNNB1 mutations and methylation profile (MethylationEPIC/Array-Illumina) were analyzed in tumoral DNA. Unsupervised machine learning analysis of this comprehensive methylome sample was achieved using hierarchical clustering and multi-dimensional scaling. Statistical associations between clusters and clinical features were achieved using Fisher's test and global biological process interpretations were aided by Gene Ontology enrichment analyses. RESULTS: Two clusters were revealed consistently by all unsupervised methods (ACP-1: n = 18; ACP-2: n = 17) with strong bootstrap statistical support. ACP-2 was enriched by CTNNB1 mutations (100% vs 56%, P = 0.0006), hypomethylated in CpG Island (CGI), non-CGI sites, and globally (P < 0.001), and associated with greater tumor size (24.1 vs 9.5cm3, P = 0.04). Enrichment analysis highlighted pathways on signaling transduction, transmembrane receptor, development of anatomical structures, cell-adhesion, cytoskeleton organization, and cytokine binding, and also cell-type specific biological processes as regulation of oligodendrocytes, keratinocyte, and epithelial cells differentiation. CONCLUSION: Two clusters of ACP patients were consistently revealed by unsupervised machine learning methods, being one of them significantly hypomethylated, enriched by CTNNB1 mutated ACPs, and associated with increased tumor size. Enrichment analysis reinforced pathways involved in tumor proliferation and in cell-specific tumoral microenvironment.

5.
Clinics ; 74: e908, 2019. tab, graf
Artigo em Inglês | LILACS | ID: biblio-1011907

RESUMO

OBJECTIVES: Approximately one-third of candidates for epilepsy surgery have no visible abnormalities on conventional magnetic resonance imaging. This is extremely discouraging, as these patients have a less favorable prognosis. We aimed to evaluate the utility of quantitative magnetic resonance imaging in patients with drug-resistant neocortical focal epilepsy and negative imaging. METHODS: A prospective study including 46 patients evaluated through individualized postprocessing of five quantitative measures: cortical thickness, white and gray matter junction signal, relaxation rate, magnetization transfer ratio, and mean diffusivity. Scalp video-electroencephalography was used to suggest the epileptogenic zone. A volumetric fluid-attenuated inversion recovery sequence was performed to aid visual inspection. A critical assessment of follow-up was also conducted throughout the study. RESULTS: In the subgroup classified as having an epileptogenic zone, individualized postprocessing detected abnormalities within the region of electroclinical origin in 9.7% to 31.0% of patients. Abnormalities outside the epileptogenic zone were more frequent, up to 51.7%. In five patients initially included with negative imaging, an epileptogenic structural abnormality was identified when a new visual magnetic resonance imaging inspection was guided by information gleaned from postprocessing. In three patients, epileptogenic lesions were detected after visual evaluation with volumetric fluid-attenuated sequence guided by video electroencephalography. CONCLUSION: Although quantitative magnetic resonance imaging analyses may suggest hidden structural lesions, caution is warranted because of the apparent low specificity of these findings for the epileptogenic zone. Conversely, these methods can be used to prevent visible lesions from being ignored, even in referral centers. In parallel, we need to highlight the positive contribution of the volumetric fluid-attenuated sequence.


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Adulto Jovem , Imageamento por Ressonância Magnética/métodos , Epilepsia Resistente a Medicamentos/diagnóstico por imagem , Mapeamento Encefálico , Estudos Prospectivos , Diagnóstico por Computador/métodos , Eletroencefalografia/métodos , Imagem Multimodal
6.
Ciênc. rural ; 43(8): 1485-1488, ago. 2013. tab
Artigo em Português | LILACS | ID: lil-680671

RESUMO

Avaliaram-se os efeitos de diferentes níveis de inclusão (0, 100, 200 e 300g kg-1 de MS) de torta de macaúba (TM) na produção leiteira e no comportamento ingestivo de oito vacas Holandesas, em dois quadrados latinos 4x4, sendo quatro tratamentos e quatro períodos experimentais. O comportamento ingestivo foi determinado mediante observações visuais, ocorridas durante 24 horas, a intervalos de 5 minutos, para determinação do tempo despendido em alimentação, ruminação e ócio. Embora tenha ocorrido redução quadrática no consumo de matéria seca e na produção de leite com a inclusão de TM nas dietas, a eficiência alimentar (gMS h-1 e gFDN h-1) e a eficiência de ruminação (gMS h-1 e gFDN h-1) foram semelhantes em todos os tratamentos. O tempo total de mastigações (min dia-1), o número de bolos ruminados (n° dia-1), o número de mastigações merícicas (n° dia-1 e n° bolo-1) e o tempo de mastigações merícicas por bolo (seg bolo-1) não apresentaram diferenças. Os resultados permitem concluir que a inclusão da torta de TM na dieta de vacas leiteiras não influencia no comportamento ingestivo dos animais, entretanto, compromete o seu desempenho.


The effects of the macauba meal (MM) inclusion (0, 100, 200 and 300g kg-1 of DM) upon daily milk production and ingestive behavior parameters were evaluated in eight Holstein cows. Animals were randomly allocated to treatments according to a replicated latin square design, with four treatments and four experimental periods. The ingestive behavior was determined by observation, during 24 hours with 5 minutes intervals to determine the time spent in feeding, rumination and idleness. There was a quadratic decrease in dry matter intake and daily milk production with MM inclusion. However, no effects were detected in MM inclusion on the feeding efficiency (gDM h-1 and gNDF h-1) and rumination efficiency (gDM h-1 and gNDF h-1). The total chewing time (min day-1), the number of ruminated (boli day-1), the ruminating chews (n. day-1 and n. boli-1) and the time of ruminating chews boli (sec boli-1) did not show any difference. The MM inclusion in the diet did not influence the ingestive behavior, but reduces the performance of animals.

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