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1.
Front Hum Neurosci ; 9: 340, 2015.
Article in English | MEDLINE | ID: mdl-26124716

ABSTRACT

Neural correlates of working memory (WM) in healthy subjects have been extensively investigated using functional MRI (fMRI). However it still remains unclear how cortical areas forming part of functional WM networks are also connected by white matter fiber bundles, and whether DTI measures, used as indices of microstructural properties and directionality of these connections, can predict individual differences in task performance. fMRI data were obtained from 23 healthy young subjects while performing one visuospatial (square location) and one visuoperceptual (face identification) 2-back task. Diffusion tensor imaging (DTI) data were also acquired. We used independent component analysis (ICA) of fMRI data to identify the main functional networks involved in WM tasks. Voxel-wise DTI analyses were performed to find correlations between structural white matter and task performance measures, and probabilistic tracking of DTI data was used to identify the white matter bundles connecting the nodes of the functional networks. We found that functional recruitment of the fusiform and the inferior frontal cortex was specific for the visuoperceptual working memory task, while there was a high overlap in brain activity maps in parietal and middle frontal areas for both tasks. Axial diffusivity and fractional anisotropy, of the tracts connecting the fusiform with the inferior frontal areas correlated with processing speed in the visuoperceptual working memory task. Although our findings need to be considered as exploratory, we conclude that both tasks share a highly-overlapping pattern of activity in areas of frontal and parietal lobes with the only differences in activation between tasks located in the fusiform and inferior frontal regions for the visuoperceptual task. Moreover, we have found that the DTI measures are predictive of the processing speed.

2.
Mov Disord ; 29(12): 1495-503, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25100674

ABSTRACT

The aim of this study was to investigate patterns of cortical atrophy associated with mild cognitive impairment in a large sample of nondemented Parkinson's disease (PD) patients, and its relation with specific neuropsychological deficits. Magnetic resonance imaging (MRI) and neuropsychological assessment were performed in a sample of 90 nondemented PD patients and 32 healthy controls. All underwent a neuropsychological battery including tests that assess different cognitive domains: attention and working memory, executive functions, memory, language, and visuoperceptual-visuospatial functions. Patients were classified according to their cognitive status as PD patients without mild cognitive impairment (MCI; n = 43) and PD patients with MCI (n = 47). Freesurfer software was used to obtain maps of cortical thickness for group comparisons and correlation with neuropsychological performance. Patients with MCI showed regional cortical thinning in parietotemporal regions, increased global atrophy (global cortical thinning, total gray matter volume reduction, and ventricular enlargement), as well as significant cognitive impairment in memory, executive, and visuospatial and visuoperceptual domains. Correlation analyses showed that all neuropsychological tests were associated with cortical thinning in parietotemporal regions and to a lesser extent in frontal regions. These results provide neuroanatomic support to the concept of MCI classified according to Movement Disorders Society criteria. The posterior pattern of atrophy in temporoparietal regions could be a structural neuroimaging marker of cognitive impairment in nondemented PD patients. All of the neuropsychological tests reflected regional brain atrophy, but no specific patterns were seen corresponding to impairment in distinct cognitive domains.


Subject(s)
Cerebral Cortex/pathology , Cognitive Dysfunction/etiology , Cognitive Dysfunction/pathology , Parkinson Disease/complications , Aged , Female , Humans , Imaging, Three-Dimensional , Magnetic Resonance Imaging , Male , Middle Aged , Neuropsychological Tests , Parkinson Disease/pathology , Severity of Illness Index , Statistics as Topic
3.
Percept Mot Skills ; 116(2): 512-27, 2013 Apr.
Article in English | MEDLINE | ID: mdl-24032327

ABSTRACT

Some people with cerebral palsy have motor and associated impairments that may hinder verbal and gestural expression to various extents. This study explores whether the ability to produce verbal or gestural expressions may be related to the comprehension of verbal communications and gestures. The influence of severity of motor impairment, general cognitive performance, and age on comprehension ability was also explored. Forty people with cerebral palsy were assigned to different groups according to their verbal and gestural expression abilities. A neuropsychological assessment of comprehension abilities and general cognitive performance was carried out. Multiple linear regression analysis was applied to identify the possible influence of expression abilities on comprehension abilities and also to detect the possible contribution of severity of motor impairment, general cognitive performance, and age. Results indicate that verbal and gestural comprehension was mainly predicted by general cognitive performance. Severity of motor impairment and age did not contribute to predicting comprehension abilities. Only verbal grammar comprehension was significantly predicted by verbal expression ability. Verbal expression ability may be an important marker for cerebral palsy therapies. In non-ambulant patients with bilateral cerebral palsy, impaired gestural expression should not be taken as an indicator of impaired gestural comprehension.


Subject(s)
Cerebral Palsy/physiopathology , Comprehension/physiology , Gestures , Verbal Behavior/physiology , Adolescent , Adult , Cerebral Palsy/psychology , Child , Female , Humans , Language Tests , Male , Neuropsychological Tests , Severity of Illness Index , Young Adult
4.
J Neurotrauma ; 30(23): 1991-4, 2013 Dec 01.
Article in English | MEDLINE | ID: mdl-23822854

ABSTRACT

Signal-intensity contrast of T1-weighted magnetic resonance imaging scans has been associated with tissue integrity and reported as a sign of neurodegenerative changes in diseases such as Alzheimer's disease. After severe traumatic brain injury (TBI), progressive structural changes occur in white (WM) and gray matter (GM). In the current study, we assessed the signal-intensity contrast of GM and WM in patients with diffuse TBI in the chronic stage to (1) characterize the regional pattern of WM/GM changes in intensity contrast associated with traumatic axonal injury, (2) evaluate possible associations between this measure and diffusion tensor image (DTI)/fractional anisotropy (FA) for detecting WM damage, and (3) investigate the correlates of both measures with cognitive outcomes. Structural T1 scans were processed with FreeSurfer software to identify the boundary and calculate the WM/GM contrast maps. DTIs were processed with the FMRIB software library to obtain FA maps. The WM/GM contrast in TBI patients showed a pattern of reduction in almost all of the brain, except the visual and motor primary regions. Global FA values obtained from DTI correlated with the intensity contrast of all associative cerebral regions. WM/GM contrast correlated with memory functions, whereas FA global values correlated with tests measuring memory and mental processing speed. In conclusion, tissue-contrast intensity is a very sensitive measure for detecting structural brain damage in chronic, severe and diffuse TBI, but is less sensitive than FA for reflecting neuropsychological sequelae, such as impaired mental processing speed.


Subject(s)
Brain Injuries/pathology , Brain/pathology , Adult , Brain Injuries/complications , Brain Injuries/psychology , Chronic Disease , Cognition Disorders/etiology , Cognition Disorders/psychology , Diffusion Tensor Imaging , Female , Glasgow Coma Scale , Humans , Image Processing, Computer-Assisted , Male , Neuropsychological Tests , Young Adult
5.
JAMA Neurol ; 70(7): 845-51, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23689958

ABSTRACT

IMPORTANCE: The study of brain activity and connectivity at rest provides a unique opportunity for the investigation of the brain substrates of cognitive outcome after traumatic axonal injury. This knowledge may contribute to improve clinical management and rehabilitation programs. OBJECTIVE: To study functional magnetic resonance imaging abnormalities in signal amplitude and brain connectivity at rest and their relationship to cognitive outcome in patients with chronic and severe traumatic axonal injury. DESIGN: Observational study. SETTING: University of Barcelona and Hospital Clinic de Barcelona, Barcelona, and Institut Guttmann-Neurorehabilitation Hospital, Badalona, Spain. PARTICIPANTS: Twenty patients with traumatic brain injury (TBI) were studied, along with 17 matched healthy volunteers. INTERVENTIONS: Resting-state functional magnetic resonance imaging and diffusion tensor imaging data were acquired. After exploring group differences in amplitude of low-frequency fluctuations (ALFF), we studied functional connectivity within the default mode network (DMN) by means of independent component analysis, followed by a dual regression approach and seed-based connectivity analyses. Finally, we performed probabilistic tractography between the frontal and posterior nodes of the DMN. MAIN OUTCOMES AND MEASURES: Signal amplitude and functional connectivity during the resting state, tractography related to DMN, and the association between signal amplitudes and cognitive outcome. RESULTS: Patients had greater ALFF in frontal regions, which was correlated with cognitive performance. Within the DMN, patients showed increased connectivity in the frontal lobes. Seed-based connectivity analyses revealed augmented connectivity within surrounding areas of the frontal and left parietal nodes of the DMN. Fractional anisotropy of the cingulate tract was correlated with increased connectivity of the frontal node of the DMN in patients with TBI. CONCLUSIONS AND RELEVANCE: Increased ALFF is related to better cognitive performance in chronic TBI. The loss of structural connectivity produced by damage to the cingulum tract explained the compensatory increases in functional connectivity within the frontal node of the DMN.


Subject(s)
Brain Injuries/pathology , Cerebral Cortex/pathology , Diffusion Tensor Imaging/methods , Magnetic Resonance Imaging/methods , Nerve Net/pathology , Adult , Anisotropy , Brain Injuries/physiopathology , Cerebral Cortex/physiopathology , Diffuse Axonal Injury/pathology , Diffuse Axonal Injury/physiopathology , Diffusion Tensor Imaging/instrumentation , Female , Frontal Lobe/pathology , Frontal Lobe/physiopathology , Gyrus Cinguli/pathology , Gyrus Cinguli/physiopathology , Humans , Magnetic Resonance Imaging/instrumentation , Male , Nerve Net/physiopathology , Neuropsychological Tests , Parietal Lobe/pathology , Parietal Lobe/physiopathology , Young Adult
6.
Behav Brain Res ; 246: 148-53, 2013 Jun 01.
Article in English | MEDLINE | ID: mdl-23458742

ABSTRACT

In non-demented older persons, smell dysfunction, measured premortem, has been associated with postmortem brain degeneration similar to that of Alzheimer's disease. We hypothesized that distinct measures of gray and white matter integrity evaluated through magnetic resonance imaging (MRI) techniques could detect degenerative changes associated with age-related olfactory dysfunction. High-resolution T1-weighted images and diffusion-tensor images (DTI) of 30 clinically healthy subjects aged 51-77 were acquired with a 3-Tesla MRI scanner. Odor identification performance was assessed by means of the University of Pennsylvania Smell Identification Test (UPSIT). UPSIT scores correlated with right amygdalar volume and bilateral perirhinal and entorhinal cortices gray matter volume. Olfactory performance also correlated with postcentral gyrus cortical thickness and with fractional anisotropy and mean diffusivity levels in the splenium of the corpus callosum and the superior longitudinal fasciculi. Our results suggest that age-related olfactory loss is accompanied by diffuse degenerative changes that might correspond to the preclinical stages of neurodegenerative processes.


Subject(s)
Olfaction Disorders/pathology , Olfactory Pathways/pathology , Smell/physiology , Aged , Anisotropy , Brain Mapping , Diffusion Magnetic Resonance Imaging , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Nerve Fibers, Myelinated/physiology , Neuroanatomy , Neuropsychological Tests , Verbal Learning/physiology
7.
Brain Stimul ; 6(1): 16-24, 2013 Jan.
Article in English | MEDLINE | ID: mdl-22410476

ABSTRACT

BACKGROUND: Verbal fluency relies on the coordinated activity between left frontal and temporal areas. Patients with Parkinson's disease (PD) present phonemic and semantic fluency deficits. Recent studies suggest that transcranial direct current stimulation (tDCS) enhances adaptative patterns of brain activity between functionally connected areas. OBJECTIVE: The aim of this study was to assess the differences in the effects induced by tDCS applied to frontal and temporo-parietal areas on phonemic and semantic fluency functional networks in patients with PD. METHOD: Sixteen patients were randomized to receive tDCS to left dorsolateral prefrontal cortex (DLPFC) and left temporo-parietal cortex (TPC) in a counterbalanced order. Immediately following stimulation, patients underwent a verbal fluency paradigm inside a fMRI scanner. Changes induced by tDCS in activation and deactivation task-related pattern networks were studied using free-model independent component analyses (ICA). RESULTS: Functional connectivity in verbal fluency and deactivation task-related networks was significantly more enhanced by tDCS to DLPFC than to TPC. In addition, DLPFC tDCS increased performance on the phonemic fluency task, after adjusting for baseline phonemic performance. CONCLUSIONS: These findings provide evidence that tDCS to specific brain regions induces changes in large scale functional networks that underlay behavioural effects, and suggest that tDCS might be useful to enhance phonemic fluency in PD.


Subject(s)
Brain/physiology , Neural Pathways/physiology , Parkinson Disease/therapy , Female , Humans , Image Interpretation, Computer-Assisted , Magnetic Resonance Imaging , Male , Middle Aged , Parkinson Disease/complications , Semantics , Speech Disorders/etiology , Speech Disorders/therapy , Transcranial Magnetic Stimulation
8.
Cortex ; 49(3): 646-57, 2013 Mar.
Article in English | MEDLINE | ID: mdl-22482692

ABSTRACT

We investigated structural brain damage in subjects who had suffered severe and diffuse traumatic brain injury (TBI), and examined its relationship with declarative memory impairment. Cortical thickness, diffusion tensor imaging (DTI), and volumetric and shape data of the hippocampus were assessed in a group of 26 adults with severe TBI in the chronic stage and 22 healthy matched controls. Declarative memory was evaluated by Rey's Auditory Verbal Learning Test (RAVLT). TBI patients performed significantly worse than controls on all RAVLT measures. The group comparison for cortical thickness and DTI revealed a pattern of widespread atrophy in TBI patients. In the TBI group DTI measures correlated with cortical thickness in the prefrontal and parietal regions, including the precuneus. Declarative memory correlated with both cortical thickness and DTI measures. However, although hippocampal volume was significantly decreased in TBI patients, no correlations were found. Multiple regression analysis of all the structural measures revealed that decreases in Fractional anisotropy (FA) and thinning of the left parietal region were the best predictors of memory impairment. In conclusion, cortical thickness reductions in the left hemisphere and a lack of white matter integrity are the main contributors to long-term impairment in declarative memory among patients suffering from severe and diffuse TBI. In this study the hippocampus did not make a significant contribution to memory dysfunctions, suggesting that damage to this structure is compensated for by other regions, with the definitive sequelae being mainly explained by alterations in cortico-subcortical connectivity.


Subject(s)
Brain Injuries/psychology , Cerebral Cortex/pathology , Hippocampus/pathology , Memory Disorders/psychology , Nerve Fibers, Myelinated/pathology , Adult , Atrophy/complications , Atrophy/pathology , Atrophy/physiopathology , Brain Injuries/complications , Brain Injuries/pathology , Brain Mapping , Cerebral Cortex/physiopathology , Diffusion Tensor Imaging , Female , Hippocampus/physiopathology , Humans , Male , Memory/physiology , Memory Disorders/etiology , Memory Disorders/pathology , Memory Disorders/physiopathology , Neuropsychological Tests , Organ Size , Verbal Learning/physiology
9.
J Neurol Neurosurg Psychiatry ; 84(4): 370-8, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23117490

ABSTRACT

BACKGROUND: In a previous functional MRI (fMRI) study, we found that patients with Parkinson's disease (PD) presented with dysfunctions in the recruitment of recognition memory networks. We aimed to investigate the changes in these networks over time. METHODS: We studied 17 PD patients and 13 age and sex matched healthy subjects. In both groups fMRI (recognition memory paradigm) and neuropsychological assessments were obtained at baseline and at follow-up. To analyse changes over time in functional networks, model free (independent component analysis) analyses of the fMRI data were carried out. Then, a cross correlation approach was used to assess the changes in the strength of functional connectivity. RESULTS: At follow-up, patients showed reduced recruitment of one network, including decreased activation in the orbitofrontal cortices, middle frontal gyri, frontal poles, anterior paracingulate cortex, superior parietal lobes and left middle temporal gyrus, as well as decreased deactivation in the anterior paracingulate gyrus and precuneus. Cross correlation analyses over time showed a decrease in the strength of functional connectivity between the middle frontal gyrus and the superior parietal lobe in PD patients. CONCLUSIONS: Model free fMRI and cross correlation connectivity analyses were able to detect progressive changes in functional networks involved in recognition memory in PD patients at early disease stages and without overt clinical deterioration. Functional connectivity analyses could be useful to monitor changes in brain networks underlying neuropsychological deficits in PD.


Subject(s)
Memory Disorders/etiology , Memory Disorders/psychology , Nerve Net/diagnostic imaging , Parkinson Disease/complications , Parkinson Disease/psychology , Recognition, Psychology/physiology , Aged , Disease Progression , Female , Fluorodeoxyglucose F18 , Humans , Image Processing, Computer-Assisted , Longitudinal Studies , Magnetic Resonance Imaging , Male , Memory Disorders/diagnostic imaging , Middle Aged , Models, Neurological , Neuropsychological Tests , Parkinson Disease/diagnostic imaging , Principal Component Analysis , Psychomotor Performance/physiology , Radionuclide Imaging , Radiopharmaceuticals , Reaction Time/physiology , Socioeconomic Factors
10.
Neuroimage ; 57(2): 589-97, 2011 Jul 15.
Article in English | MEDLINE | ID: mdl-21554963

ABSTRACT

We aimed to investigate changes in the verbal recognition memory network in patients with early Parkinson's disease (PD) without overt recognition memory alteration. Verbal recognition memory was assessed in 24 PD patients in early stages of the disease and a control group of 24 healthy subjects during fMRI data acquisition. Participants were presented with a list of 35 words before imaging, and later during fMRI scanning they were required to recognize these previously presented words. Both model-based (FEAT) and model-free (MELODIC) analyses of the fMRI data were carried out with FSL software. Memory was also assessed by means of Rey's Auditory Verbal Learning Test (RAVLT). PD patients showed no difference in the fMRI recognition memory task and recognition memory assessed by the RAVLT compared to healthy controls. Model-based analysis did not show significant differences between groups. On the other hand, model-free analysis identified components that fitted the task-model and were common to all the participants, as well as components that differed between PD and healthy controls. PD patients showed decreased task-related activations in areas involved in the recognition memory network and decreased task-related deactivations in the default mode network in comparison with controls. In conclusion, model-free fMRI analysis detected alterations in functional cerebral networks involved in a verbal memory task in PD patients without evident recognition memory deficit.


Subject(s)
Cerebral Cortex/physiopathology , Memory Disorders/physiopathology , Neural Pathways/physiopathology , Parkinson Disease/physiopathology , Adult , Aged , Early Diagnosis , Female , Humans , Image Interpretation, Computer-Assisted , Magnetic Resonance Imaging , Male , Memory Disorders/diagnosis , Memory Disorders/etiology , Middle Aged , Neuropsychological Tests , Parkinson Disease/complications , Parkinson Disease/diagnosis , Recognition, Psychology/physiology
11.
BMC Neurol ; 11: 24, 2011 Feb 23.
Article in English | MEDLINE | ID: mdl-21345223

ABSTRACT

BACKGROUND: Memory is one of the most impaired functions after traumatic brain injury (TBI). We used diffusion tensor imaging (DTI) to determine the structural basis of memory deficit. We correlated fractional anisotropy (FA) of the fasciculi connecting the main cerebral regions that are involved in declarative and working memory functions. METHODS: Fifteen patients with severe and diffuse TBI and sixteen healthy controls matched by age and years of education were scanned. The neuropsychological assessment included: Letter-number sequencing test (LNS), 2-back task, digit span (forwards and backwards) and the Rivermead profilet. DTI was analyzed by a tract-based spatial statics (TBSS) approach. RESULTS: Whole brain DTI analysis showed a global decrease in FA values that correlated with the 2-back d-prime index, but not with the Rivermead profile. ROI analysis revealed positive correlations between working memory performance assessed by 2-back d-prime and superior longitudinal fasciculi, corpus callosum, arcuate fasciculi and fornix. Declarative memory assessed by the Rivermead profile scores correlated with the fornix and the corpus callosum. CONCLUSIONS: Diffuse TBI is associated with a general decrease of white matter integrity. Nevertheless deficits in specific memory domains are related to different patterns of white matter damage.


Subject(s)
Brain Injuries/pathology , Brain Injuries/psychology , Diffusion Tensor Imaging/methods , Memory Disorders/pathology , Nerve Fibers, Myelinated/pathology , Neural Pathways/pathology , Adolescent , Adult , Anisotropy , Brain Injuries/complications , Brain Mapping/methods , Cross-Sectional Studies , Female , Humans , Male , Memory Disorders/complications , Neuropsychological Tests
12.
Mov Disord ; 25(12): 1888-94, 2010 Sep 15.
Article in English | MEDLINE | ID: mdl-20669268

ABSTRACT

Olfactory dysfunction is known to occur before the appearance of the classical motor signs in Parkinson's disease (PD) and diffusion tensor imaging (DTI) studies in PD have reported fractional anisotropy (FA) reductions in the early disease stages. We aimed to investigate the relationship between olfactory dysfunction and white matter (WM) FA of central olfactory areas in early PD. Twenty-four patients at Hoehn and Yahr stages I and II and 24 healthy controls matched by age, gender and years of education participated in this study. DTI was acquired at a 3 Tesla scanner and odor identification was assessed using the University of Pennsylvania Smell Identification Test (UPSIT). We performed FA voxelwise group comparisons in the central olfactory structures using tract-based spatial statistics (TBSS) and correlation analyses between FA values in these central olfactory areas and UPSIT scores. Patients with severe microsmia (UPSIT between 19 and 25) and anosmia (UPSIT lower or equal to 18) had lower FA values than PD patients with mild/moderate or no olfactory dysfunction (UPSIT between 26 and 40) and healthy controls in the WM adjacent to gyrus rectus. In addition, patients with anosmia had reduced FA in the WM surrounding primary olfactory areas in comparison with healthy controls. FA values in the WM adjacent to primary olfactory cortex and right gyrus rectus correlated with UPSIT scores in the PD group. This study demonstrates, for the first time, that microstructural WM reductions are present in the central olfactory system of early stage PD patients and that these reductions are associated with reduced ability to smell.


Subject(s)
Nerve Fibers, Myelinated/pathology , Olfaction Disorders/physiopathology , Olfactory Pathways/physiopathology , Parkinson Disease/physiopathology , Smell , Adult , Aged , Analysis of Variance , Brain Mapping , Diffusion Tensor Imaging , Female , Functional Laterality , Humans , Image Processing, Computer-Assisted , Male , Middle Aged , Olfaction Disorders/complications , Olfaction Disorders/pathology , Olfactory Pathways/pathology , Parkinson Disease/complications , Parkinson Disease/pathology , Regression Analysis
13.
J Neurotrauma ; 27(7): 1187-93, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20392136

ABSTRACT

The thalamus is known to play a key role in arousal regulation and support of human consciousness. Neuropathological studies have identified thalamic damage as one of the most common abnormalities present in the brains of patients who were in a vegetative state (VS) or a minimally-conscious state (MCS) state at the time of their deaths. Nonetheless, no in vivo studies of thalamic abnormalities in these patients have been conducted. Using high-resolution T1-weighted magnetic resonance images and a novel approach to shape analysis, we investigated thalamic global and regional changes in a sample of patients in a VS or an MCS. Group comparisons and correlations with clinical variables were performed for the total thalamic volume and for each surface vertex. Total thalamic volume was significantly lower in patients than in healthy volunteers. Shape analysis revealed significant bilateral regional atrophy in the dorso-medial body in patients compared to controls; this atrophy was more widespread in VS than in MCS patients. Lower thalamic volume was significantly correlated with worse Disability Rating Scale scores. Shape analysis suggested that the dorso-medial nucleus and the internal medullar lamina were the main regions responsible for this correlation. Our findings suggest that MCS and VS patients present different patterns of regional thalamic abnormalities, and that these differences partially explain their clinical profile.


Subject(s)
Persistent Vegetative State/pathology , Thalamus/pathology , Adolescent , Adult , Atrophy , Brain Mapping , Disability Evaluation , Female , Humans , Magnetic Resonance Imaging , Male , Mediodorsal Thalamic Nucleus/pathology , Mediodorsal Thalamic Nucleus/physiopathology , Middle Aged , Nerve Fibers, Myelinated/pathology , Persistent Vegetative State/physiopathology , Severity of Illness Index , Thalamus/physiopathology , Young Adult
14.
Int J Dev Neurosci ; 27(6): 559-65, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19563880

ABSTRACT

Premature birth is associated with several brain dysfunctions including changes in the normal pattern of sulcal development. Previous studies on sulcal abnormalities were performed in subjects with perinatal brain complications. We selected a sample of preterm subjects with a low risk of neurodevelopmental abnormalities with the aim of investigating the effects of prematurity per se. Surface and maximum depth measures of four sulci that develop at different gestational ages were obtained using Anatomist/Brain Visa 3.0.2 software. The sulci measured were the olfactory sulcus (16 weeks), the parieto-occipital sulcus (22-23 weeks), the superior temporal sulcus (32 weeks) and the orbitofrontal sulcus (36-39 weeks). The sample comprised 17 low-risk preterms (mean gestational age: 32 weeks) and 16 full-term children who were matched for age at scan, gender, handedness and socio-cultural status. Analysis of surface variance showed a significant group effect (P<0.015), as well as an interaction between the type of sulcus and group (P<0.001). The superior temporal sulcus surface was inferior in the low-risk preterm group compared to controls. Our findings suggest that even without perinatal complications, premature birth affects sulcal morphology.


Subject(s)
Cerebral Cortex/abnormalities , Cerebral Cortex/physiopathology , Nervous System Malformations/physiopathology , Premature Birth/physiopathology , Child , Cognition Disorders/diagnosis , Cognition Disorders/etiology , Cognition Disorders/physiopathology , Cohort Studies , Female , Gestational Age , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Male , Nervous System Malformations/etiology , Neuropsychological Tests , Organ Size/physiology , Prefrontal Cortex/abnormalities , Prefrontal Cortex/physiopathology , Risk Factors , Software , Temporal Lobe/abnormalities , Temporal Lobe/physiopathology
15.
Eur Arch Psychiatry Clin Neurosci ; 259(4): 203-11, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19224116

ABSTRACT

Schizophrenia is a major mental disorder which is characterized by several cognitive deficits. Investigations of the neural basis of memory dysfunctions using neuroimaging techniques suggest that the hippocampus plays an important role in declarative memory impairment. The goal of this study was to investigate possible dysfunctions in cerebral activation in schizophrenic patients during both word and face recognition memory tasks. We tested 22 schizophrenics and 24 controls matched by gender, age, handedness and parental socioeconomic status. Compared to healthy volunteers, patients with schizophrenia showed decreased bilateral hippocampal activation during word and face recognition tasks. The whole brain analysis also showed a pattern of cortical and subcortical hypoactivation for both verbal and non-verbal recognition. This study provides further evidence of hippocampal involvement in declarative memory impairments of schizophrenia.


Subject(s)
Face , Hippocampus/physiopathology , Magnetic Resonance Imaging , Recognition, Psychology , Schizophrenia/physiopathology , Verbal Learning , Adult , Case-Control Studies , Female , Humans , Male , Pattern Recognition, Visual , Photic Stimulation/methods , Psychiatric Status Rating Scales , Reaction Time , Schizophrenia/diagnosis , Semantics
16.
Neurobiol Aging ; 30(7): 1114-24, 2009 Jul.
Article in English | MEDLINE | ID: mdl-18053618

ABSTRACT

Cognitive reserve (CR) is the brain's capacity to cope with cerebral damage to minimize clinical manifestations. The 'passive model' considers head or brain measures as anatomical substrates of CR, whereas the 'active model' emphasizes the use of brain networks effectively. Sixteen healthy subjects, 12 amnestic mild cognitive impairment (MCI) and 16 cases with mild Alzheimer's disease (AD) were included to investigate the relationships between proxies of CR and cerebral measures considered in the 'passive' and 'active' models. CR proxies were inferred premorbid IQ (WAIS Vocabulary test), 'education-occupation', a questionnaire of intellectual and social activities and a composite CR measure. MRI-derived whole-brain volumes and brain activity by functional MRI during a visual encoding task were obtained. Among healthy elders, higher CR was related to larger brains and reduced activity during cognitive processing, suggesting more effective use of cerebral networks. In contrast, higher CR was associated with reduced brain volumes in MCI and AD and increased brain function in the latter, indicating more advanced neuropathology but that active compensatory mechanisms are still at work in higher CR patients. The right superior temporal gyrus (BA 22) and the left superior parietal lobe (BA 7) showed greatest significant differences in direction of slope with CR and activation between controls and AD cases. Finally, a regression analysis revealed that fMRI patterns were more closely related to CR proxies than brain volumes. Overall, inverse relationships for healthy and pathological aging groups emerged between brain structure and function and CR variables.


Subject(s)
Aging/pathology , Alzheimer Disease/pathology , Brain/pathology , Cognition Disorders/pathology , Aged , Aging/psychology , Alzheimer Disease/physiopathology , Alzheimer Disease/psychology , Brain/physiopathology , Brain Mapping , Cognition Disorders/physiopathology , Cognition Disorders/psychology , Disability Evaluation , Female , Humans , Intelligence Tests , Magnetic Resonance Imaging , Male , Models, Neurological , Nerve Net/physiology , Neural Pathways/physiology , Neuronal Plasticity/physiology , Neuropsychological Tests , Parietal Lobe/anatomy & histology , Parietal Lobe/physiology , Reference Values , Severity of Illness Index , Surveys and Questionnaires , Temporal Lobe/anatomy & histology , Temporal Lobe/physiology
17.
Pediatr Neurol ; 40(1): 19-26, 2009 Jan.
Article in English | MEDLINE | ID: mdl-19068249

ABSTRACT

The lower-than-average cognitive performance of individuals with bilateral cerebral palsy found in previous studies does not always refer to an abnormal performance or clinically significant impairment. We aimed to establish the percentage of persons with bilateral cerebral palsy who present neuropsychologic impairment, and its relationship to perinatal data and motor signs. Forty children, adolescents, and adults (age range, 6-38 years; 15 females and 25 males) with bilateral cerebral palsy were neuropsychologically assessed. Vocabulary was impaired in 85% of participants, language comprehension in 13-48%, visuoperceptual abilities in 60%, visuospatial abilities in 90%, short-term memory in 21-58%, declarative memory in 47-67%, and praxis comprehension in 20%, with executive deficits in 58-74%. Perinatal data (intrauterine growth and birth weight) contributed to explaining memory impairment. Among cerebral palsy subtypes (spastic, mixed, and dyskinetic), forms of impairment differed only in short-term verbal memory. No persons with dyskinetic cerebral palsy experienced impairment in immediate memory or working visual memory. We conclude that visuospatial deficit is the most frequent impairment in people with bilateral cerebral palsy. Moreover, short-term memory impairment seems sensitive to perinatal complications, and differs among bilateral cerebral palsy subtypes.


Subject(s)
Cerebral Palsy/classification , Cerebral Palsy/psychology , Memory , Space Perception , Visual Perception , Adolescent , Adult , Birth Weight , Cerebral Palsy/diagnosis , Cerebral Palsy/physiopathology , Child , Cognition , Female , Humans , Male , Memory/classification , Neuropsychology , Verbal Learning , Vocabulary , Young Adult
18.
Brain Inj ; 22(11): 882-90, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18850346

ABSTRACT

PRIMARY OBJECTIVE: To study cerebral response in a functional magnetic resonance imaging (fMRI) task of speech perception in a sample of patients in vegetative state (VS) and minimally conscious state (MCS) after traumatic brain injury. METHODS: Three patients in VS, four patients in MCS and 19 healthy volunteers were enrolled for the study. All subjects underwent an fMRI task of passive listening of narratives played forward and backward, alternated with periods of silence. This study analysed cerebral response to language and to complex sound processing in the healthy subjects' group and in each patient, using SPM5. RESULTS: One patient in VS and one in MCS showed cerebral responses to language and to complex sound very similar to those shown by the healthy volunteers. Two more patients, one in VS and one in MCS, showed significant responses to complex sound only. Finally, one patient in VS and one patient in MCS failed to show significant activation in response to either stimulus. CONCLUSIONS: Some patients in VS and MCS can preserve cerebral responses to language and auditory stimuli. fMRI may be useful to identify these responses, which may pass unnoticed in a bedside examination.


Subject(s)
Brain Injuries/psychology , Consciousness/physiology , Persistent Vegetative State/physiopathology , Acoustic Stimulation/methods , Adolescent , Adult , Auditory Perception/physiology , Awareness , Brain Injuries/complications , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Persistent Vegetative State/diagnosis , Speech Perception/physiology
19.
Neuroimage ; 43(3): 421-9, 2008 Nov 15.
Article in English | MEDLINE | ID: mdl-18771738

ABSTRACT

Traumatic brain injury (TBI) patients have working memory deficits and altered patterns of brain activation during this function. The evolution of the impairment has not been examined to date. This study investigated longitudinal changes in brain activation during a working memory task. Twelve patients with severe and diffuse TBI and ten healthy matched controls were fMRI scanned twice at a 6-month interval during an n-back task (0-, 2- and 3-back). All the TBI patients selected presented signs of diffuse axonal injury on CT but had no evidence of focal lesions on MRI clinical examination. Significant changes in brain activation over time were observed in patients, but not in controls. During the first examination, though both groups engaged bilateral fronto-parietal regions known to be involved in working memory, activation of the right superior frontal gyrus was low in the TBI group. However, the difference between TBI and controls had decreased significantly after 6 months. A factor analysis confirmed the greater increase in activation in the right superior frontal cortex in the TBI group than in healthy controls, leading to normalization of the brain activation pattern. In conclusion, this longitudinal study provides evidence of a progressive normalization of the working memory activation pattern after diffuse axonal injury in severe TBI, coinciding with an improvement in performance on this function.


Subject(s)
Brain Mapping , Diffuse Axonal Injury/physiopathology , Magnetic Resonance Imaging , Memory Disorders/physiopathology , Adult , Brain Injuries/complications , Brain Injuries/physiopathology , Diffuse Axonal Injury/complications , Female , Humans , Image Processing, Computer-Assisted , Longitudinal Studies , Male , Memory Disorders/etiology , Memory, Short-Term/physiology , Neuropsychological Tests
20.
Neurobiol Aging ; 29(11): 1644-53, 2008 Nov.
Article in English | MEDLINE | ID: mdl-17560689

ABSTRACT

The purpose of the present study was to evaluate functional connectivity of the hippocampus during a fMRI face-name learning task in a group of elders with mild memory impairment on the basis of the presence or absence of the APOE epsilon4 allele. Twelve epsilon4 carriers and 20 non-carriers with mild memory dysfunction and exhibiting equivalent performance in clinical evaluations of global cognitive function and memory were studied. Subjects underwent a fMRI session consisting of a face-name encoding memory task. Following scanning, subjects were asked to pair faces with their corresponding proper name. Functional connectivity of the hippocampus was measured by using coherence analysis to evaluate the activity of brain circuits related to memory encoding processes. In contrast to non-APOE epsilon4 allele bearers, APOE epsilon4 carriers showed enhanced connectivity with the anterior cingulate, inferior parietal/postcentral gyrus region and the caudate nucleus. Enhanced hippocampal connectivity with additional brain regions in APOE epsilon4 allele carriers during the performance of an associative memory task may reveal the existence of additional activity in the cortico-subcortical network engaged during memory encoding in subjects carrying this genetic variant.


Subject(s)
Apolipoprotein E3/genetics , Hippocampus/physiopathology , Memory Disorders/physiopathology , Memory , Nerve Net/physiopathology , Aged , Brain Mapping , Female , Genetic Predisposition to Disease/genetics , Humans , Magnetic Resonance Imaging , Male , Memory Disorders/genetics
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