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1.
Br J Ophthalmol ; 106(6): 870-877, 2022 06.
Artigo em Inglês | MEDLINE | ID: mdl-33468491

RESUMO

AIMS: The purpose of this study was to explore the microstructural properties of the major white matter (WM) tracts in constant exotropia (XT) before and after strabismus surgery, and further investigate the association between microstructural alterations and the ocular dominance (OD). METHODS: We collected diffusion tensor imaging data of patients with XT before (n=19) and after (n=15) strabismus surgery and 20 healthy controls and evaluated OD and stereopsis. The probabilistic streamline tractography of the 24 major WM tracts was reconstructed by using the automated fibre quantification package. Fractional anisotropy and mean diffusivity (MD) along each tract were estimated, and their differences between the groups were examined. Furthermore, we evaluated the relationship between OD and the absolute value of altered microstructural parameters. RESULTS: While all postoperative XT patients restored normal stereopsis, most of their OD remained aberrant (9 out of 11). Compared with that of preoperation, the MD of postoperative patients decreased significantly along left anterior thalamic radiation (ATR), left arcuate fasciculus (AF), left corticospinal tract (CST), left cingulum cingulate (CGC) and left inferior fronto-occipital fasciculus. Moreover, OD was negatively correlated with the absolute value of MD changes in left ATR, left AF, left CST and left CGC. CONCLUSION: Microstructural alterations after surgery in the visuospatial network tracts may contribute to the stereopsis restoration. Additionally, the results of the correlation analysis may signify that the balanced binocular input may be more conducive for the restoration and improvement of binocular visual function, including stereopsis. Thus, restoring normal ocular balance after surgical correction may be necessary to achieve more substantial improvements.


Assuntos
Exotropia , Substância Branca , Anisotropia , Imagem de Tensor de Difusão/métodos , Exotropia/cirurgia , Humanos , Substância Branca/diagnóstico por imagem
2.
Exp Gerontol ; 140: 111060, 2020 10 15.
Artigo em Inglês | MEDLINE | ID: mdl-32814097

RESUMO

INTRODUCTION: Numerous structural studies have already reported volumetric reduction in cerebellum with aging. However, there are still limited studies particularly focusing on analysis of the cerebellar resting state FC in old adults. Even so, the least related studies were unable to include some important cerebellar lobules due to limited cerebellum segmentation methods. OBJECTIVE: The purpose of this study is to explore cognitive function in relation to cerebellar lobular morphometry and cortico-cerebellar connectivity changes in old adults' lifespan by incorporating previously undetected cerebellar lobules. METHODS: This study includes a sample of 264 old adults subdivided into five cognitively normal age groups (G1 through G5). Cerebellum Segmentation (CERES) software was used to obtain morphometric measures and brain masks of all the 24 cerebellar lobules. We then defined individual lobules as seed regions and mapped the whole-brain to get functional connectivity maps. To analyze age group differences in cortico-cerebellar connectivity and cerebellar lobular volume, we used one way ANOVA and post hoc analysis was performed for multiple comparisons using Bonferroni method. RESULTS: Our results report cerebellar lobular volumetric reduction, disrupted intra-cerebellar connectivity and significant differences in cortico-cerebellar resting state FC across age groups. In addition, our results show that disrupted FC between left Crus-II and right ACC relates to well emotion regulation and cognitive decline and is associated with poor performance on TMT-B and logical memory tests in older adults. CONCLUSION: Overall, our findings confirm that as humans get older and older, the cerebellar lobular volumes as well as the cortico-cerebellar functional connectivity are affected and hence reduces cognition.


Assuntos
Mapeamento Encefálico , Imageamento por Ressonância Magnética , Idoso , Cerebelo/diagnóstico por imagem , Cognição , Humanos , Vias Neurais
3.
Front Neurol ; 11: 606592, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-33519683

RESUMO

Purpose: Previous studies have shown that HIV affects striato-cortical regions, leading to persisting cognitive impairment in 30-70% of the infected individuals despite combination antiretroviral therapy. This study aimed to investigate brain functional dynamics whose deficits might link to early cognitive decline or immunologic deterioration. Methods: We applied sliding windows and K-means clustering to fMRI data (HIV patients with asymptomatic neurocognitive impairment and controls) to construct dynamic resting-state functional connectivity (RSFC) maps and identify states of their reoccurrences. The average and variability of dynamic RSFC, and the dwelling time and state transitioning of each state were evaluated. Results: HIV patients demonstrated greater variability in RSFC between the left pallidum and regions of right pre-central and post-central gyri, and between the right supramarginal gyrus and regions of the right putamen and left pallidum. Greater variability was also found in the frontal RSFC of pars orbitalis of the left inferior frontal gyrus and right superior frontal gyrus (medial). While deficits in learning and memory recall of HIV patients related to greater striato-sensorimotor variability, deficits in attention and working memory were associated with greater frontal variability. Greater striato-parietal variability presented a strong link with immunologic function (CD4+/CD8+ ratio). Furthermore, HIV-infected patients exhibited longer time and reduced transitioning in states typified by weaker connectivity in specific networks. CD4+T-cell counts of the HIV-patients were related to reduced state transitioning. Conclusion: Our findings suggest that HIV alters brain functional connectivity dynamics, which may underlie early cognitive impairment. These findings provide novel insights into our understanding of HIV pathology, complementing the existing knowledge.

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