Search

Introduction: In this study, we intend to determine the correlation between the thickness of the cerebral cortex and the severity of the cognitive disorder in Alzheimer disease (AD). Methods: A total of 20 (14 women and 6 men) patients diagnosed with AD with a Mean age of 72.95 years, and 10 (7 women and 3 men) cognitively normal (CN) subjects with a Mean age of 70.50 years were included in the study. Of the AD patient and CN subjects, 70% were female, and 30% were male. All individuals underwent 1.5 T Magnetic resonance imaging (MRI). The MRI scanning protocol included 3D MPRAGE (3D-T1W) sequence. All images were analyzed using Freesurfer v5.3, and then the brain cortical thickness in 7 cortical areas (inferior temporal, middle temporal, superior temporal, parahippocampal, pars triangularis, rostral middle frontal, and superior frontal) was calculated. Results: The analysis of covariance (ANCOVA) was conducted to compare the mean thickness of each region between the patient and the control group. There was a significant difference in the mean cortical thickness in all regions. In all cases, the mean cortical thickness in CN subjects was greater than in AD patients. However, the mean thickness of pars triangularis left hand in CN subjects was not significantly greater than that in AD patients. The receiver operating characteristic system (ROC) was designed to evaluate the predictive power of the patients and the healthy people. We have selected a thousand cut-off points from 1.5 to 3.5 mm for cortical thickness. When the cut-off points were within 2.276878–2.299680 mm in the left hemisphere, Youden’s index was maximum. The sensitivity and specificity, in this case, were 80%. Also, when the cut-off points were within the range of 2.263278–2.282278 mm in the right hemisphere, the sensitivity and specificity were 90% and 80%, respectively. Conclusion: This study demonstrates the importance of quantifying the cortical thickness changes in the early diagnosis of AD. In addition, examining the pattern of changes and quantifying the reduction in the thickness of the cortex is a crucial tool for displaying the local and global atrophy of the brain. Also, this pattern can be used as an alternative marker for the diagnosis of dementia. Finally, to the best of our knowledge, our study is the first to report finding on the cortical thickness that would help the clinician have a better differential diagnosis. Also, this study has checked the possibility of early diagnosis of the disease.

Introduction: In this study, we intend to determine the correlation between the thickness of the cerebral cortex and the severity of the cognitive disorder in Alzheimer disease (AD). Methods: A total of 20 (14 women and 6 men) patients diagnosed with AD with a Mean age of 72.95 years, and 10 (7 women and 3 men) cognitively normal (CN) subjects with a Mean age of 70.50 years were included in the study. Of the AD patient and CN subjects, 70% were female, and 30% were male. All individuals underwent 1.5 T Magnetic resonance imaging (MRI). The MRI scanning protocol included 3D MPRAGE (3D-T1W) sequence. All images were analyzed using Freesurfer v5.3, and then the brain cortical thickness in 7 cortical areas (inferior temporal, middle temporal, superior temporal, parahippocampal, pars triangularis, rostral middle frontal, and superior frontal) was calculated. Results: The analysis of covariance (ANCOVA) was conducted to compare the mean thickness of each region between the patient and the control group. There was a significant difference in the mean cortical thickness in all regions. In all cases, the mean cortical thickness in CN subjects was greater than in AD patients. However, the mean thickness of pars triangularis left hand in CN subjects was not significantly greater than that in AD patients. The receiver operating characteristic system (ROC) was designed to evaluate the predictive power of the patients and the healthy people. We have selected a thousand cut-off points from 1.5 to 3.5 mm for cortical thickness. When the cut-off points were within 2.276878-2.299680 mm in the left hemisphere, Youden's index was maximum. The sensitivity and specificity, in this case, were 80%. Also, when the cut-off points were within the range of 2.263278-2.282278 mm in the right hemisphere, the sensitivity and specificity were 90% and 80%, respectively. Conclusion: This study demonstrates the importance of quantifying the cortical thickness changes in the early diagnosis of AD. In addition, examining the pattern of changes and quantifying the reduction in the thickness of the cortex is a crucial tool for displaying the local and global atrophy of the brain. Also, this pattern can be used as an alternative marker for the diagnosis of dementia. Finally, to the best of our knowledge, our study is the first to report finding on the cortical thickness that would help the clinician have a better differential diagnosis. Also, this study has checked the possibility of early diagnosis of the disease. [ABSTRACT FROM AUTHOR]

ObjectiveThis study aimed to investigate the morphometric alterations in the cortical and subcortical structures in multiple system atrophy (MSA) patients with mild cognitive impairment (MCI), and to explore the association with cognitive deficits.MethodsA total of 45 MSA patients (25 MSA-only, 20 MSA-MCI) and 29 healthy controls were recruited. FreeSurfer software was used to analyze cortical thickness, and voxel-based morphometry was used to analyze the gray matter volumes. Cortical thickness and gray matter volume changes were correlated with cognitive scores.ResultsCompared to healthy controls, both MSA subgroups exhibited widespread morphology alterations of brain structures in the fronto-temporal regions. Direct comparison of MSA-MCI and MSA-only patients showed volume reduction in the left superior and middle temporal gyrus, while cortical thinning was found in the left middle and inferior temporal gyrus in MSA-MCI patients. Cortical thinning in the left middle temporal gyrus correlated with cognitive assessment and disease duration.ConclusionStructural changes in the brain occur in MSA-MCI patients. The alteration of brain structure in the left temporal regions might be a biomarker of cognitive decline in MSA-MCI patients.

Objective: This study aimed to investigate the morphometric alterations in the cortical and subcortical structures in multiple system atrophy (MSA) patients with mild cognitive impairment (MCI), and to explore the association with cognitive deficits. Methods: A total of 45 MSA patients (25 MSA-only, 20 MSA-MCI) and 29 healthy controls were recruited. FreeSurfer software was used to analyze cortical thickness, and voxel-based morphometry was used to analyze the gray matter volumes. Cortical thickness and gray matter volume changes were correlated with cognitive scores. Results: Compared to healthy controls, both MSA subgroups exhibited widespread morphology alterations of brain structures in the fronto-temporal regions. Direct comparison of MSA-MCI and MSA-only patients showed volume reduction in the left superior and middle temporal gyrus, while cortical thinning was found in the left middle and inferior temporal gyrus in MSA-MCI patients. Cortical thinning in the left middle temporal gyrus correlated with cognitive assessment and disease duration. Conclusion: Structural changes in the brain occur in MSA-MCI patients. The alteration of brain structure in the left temporal regions might be a biomarker of cognitive decline in MSA-MCI patients. [ABSTRACT FROM AUTHOR]

Background: Neurological soft signs (NSS), i.e. subtle neurological abnormalities, have been frequently found in schizophrenia. Neuroimaging studies in schizophrenia have shown abnormal cortical thickness changes across the cortical mantle. However, few studies have examined relationships between NSS and cortical thickness abnormalities in schizophrenia. Method: A sample of 18 patients with chronic schizophrenia and 20 age-matched healthy controls were included. Cortical thickness was assessed on high-resolution 3-tesla magnetic resonance imaging by using FreeSurfer software and NSS were rated on the Heidelberg Scale. Results: Significant negative correlations between NSS and cortical thickness were found in the prefrontal, inferior temporal, superior parietal, postcentral, and supramarginal cortices in the schizophrenia patients. In the controls, however, this negative correlation was found in the anterior cingulate, pericalcarine and superior/middle temporal regions. Conclusion: Our results not only confirmed the association between NSS and cortical thickness in chronic schizophrenia but also indicated that patients and controls have different anatomical substrates of NSS. © 2015 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]