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2.
Hum Brain Mapp ; 37(5): 1953-69, 2016 May.
Article in English | MEDLINE | ID: mdl-27012301

ABSTRACT

Reasoning by analogy allows us to link distinct domains of knowledge and to transfer solutions from one domain to another. Analogical reasoning has been studied using various tasks that have generally required the consideration of the relationships between objects and their integration to infer an analogy schema. However, these tasks varied in terms of the level and the nature of the relationships to consider (e.g., semantic, visuospatial). The aim of this study was to identify the cerebral network involved in analogical reasoning and its specialization based on the domains of information and task specificity. We conducted a coordinate-based meta-analysis of 27 experiments that used analogical reasoning tasks. The left rostrolateral prefrontal cortex was one of the regions most consistently activated across the studies. A comparison between semantic and visuospatial analogy tasks showed both domain-oriented regions in the inferior and middle frontal gyri and a domain-general region, the left rostrolateral prefrontal cortex, which was specialized for analogy tasks. A comparison of visuospatial analogy to matrix problem tasks revealed that these two relational reasoning tasks engage, at least in part, distinct right and left cerebral networks, particularly separate areas within the left rostrolateral prefrontal cortex. These findings highlight several cognitive and cerebral differences between relational reasoning tasks that can allow us to make predictions about the respective roles of distinct brain regions or networks. These results also provide new, testable anatomical hypotheses about reasoning disorders that are induced by brain damage. Hum Brain Mapp 37:1953-1969, 2016. © 2016 Wiley Periodicals, Inc.


Subject(s)
Brain Mapping , Brain/physiology , Concept Formation/physiology , Semantics , Brain/diagnostic imaging , Functional Laterality , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging , Problem Solving , Space Perception/physiology
3.
Neurocase ; 22(2): 168-9, 2016.
Article in English | MEDLINE | ID: mdl-26304673

ABSTRACT

We report the case of a 78-year-old patient admitted to the hospital for behavioral and psychological disorders consisting in impressions of presence of a stranger located behind the bathroom mirror, who strikingly shared the patient's appearance but was considered a different person, yet. We discuss how this case can be interpreted as an atypical Capgras syndrome for his mirror image and how it suggests an adjustment of the classical dual-route model that sustains face recognition between covert (or affective) and overt neural pathways.


Subject(s)
Capgras Syndrome/physiopathology , Capgras Syndrome/psychology , Recognition, Psychology/physiology , Self Concept , Aged , Brain/pathology , Brain/physiopathology , Delusions , Electroencephalography , Face , Humans , Male
4.
Drugs Aging ; 32(11): 917-26, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26446151

ABSTRACT

INTRODUCTION: The use of intravenous thrombolysis with alteplase for ischemic stroke in Europe is restricted to subjects aged <80 years. Recent studies have reported the efficacy and safety of alteplase in older patients. However, data concerning the quality of life (QOL) of these elderly subjects are sparse. OBJECTIVES: The aim of this study was to compare the QOL of patients aged ≥80 years with that of patients aged <80 years at 3 months after thrombolysis. METHOD: This was a prospective study comprising French-speaking patients aged >18 years treated using thrombolytic therapy for ischemic stroke at the Hospital of Tours (Tours, France) between June 2012 and January 2013. QOL was assessed using the Stroke Impact Scale (SIS). The presence of mood disorders or cognitive impairments was also assessed. RESULTS: QOL was evaluated for 62 subjects among the 83 enrolled patients who received thrombolytic treatment; 21 patients were aged >80 years. Concerning scores on the SIS, using a multivariate analysis, only the memory and thinking score was significantly and negatively associated with the elderly population [odds ratio (OR) 0.036, 95% confidence interval (CI) 0.004-0.339; p = 0.004]. No significant difference was observed among all the other QOL scores. Neurological recovery and functional status did not differ between the two groups. CONCLUSION: QOL after intravenous thrombolysis in the elderly population was comparable to that of younger subjects. Despite its small sample size, this study showed promising results in favor of intravenous thrombolysis in the elderly population and highlighted the importance of systematic screening for post-stroke cognitive impairment, particularly in this population.


Subject(s)
Brain Ischemia/drug therapy , Off-Label Use , Quality of Life , Stroke/drug therapy , Thrombolytic Therapy/adverse effects , Tissue Plasminogen Activator/therapeutic use , Administration, Intravenous , Adult , Age Factors , Aged , Aged, 80 and over , Brain Ischemia/complications , Cognition Disorders/complications , Female , Fibrinolytic Agents/administration & dosage , Fibrinolytic Agents/therapeutic use , Humans , Male , Middle Aged , Mood Disorders/complications , Prospective Studies , Stroke/complications , Time Factors , Tissue Plasminogen Activator/administration & dosage , Treatment Outcome
5.
J Neurol Sci ; 337(1-2): 212-4, 2014 Feb 15.
Article in English | MEDLINE | ID: mdl-24296360

ABSTRACT

INTRODUCTION: Whether motor neuron diseases (MNDs) can be considered in some cases of paraneoplastic syndromes is controversial. We report a case of rapidly progressive motor neuronopathy following a diagnosis of breast carcinoma, with a presence of anti-Ri antibodies, and a novel SOD1 gene mutation. OBSERVATION: An 80-year-old woman with mucinous adenocarcinoma of the left breast for 4 years developed sub-acute quadriparesis. Myography revealed chronic denervation signs. The patient had serum anti-Ri onconeural antibodies. The diagnosis of paraneoplastic MND was established. Because of a familial history of ALS, a genetic analysis for familial ALS was performed. We identified a novel heterozygous mutation in SOD1 gene, SOD I18del. This mutation may reflect a genetic predisposition to develop a MND, inducing fragility of motor neurons. Neurological improvement was observed after three months of both intravenous gamma globulin and corticosteroids. CONCLUSION: The present observation supports the idea that MND can be considered as a paraneoplastic syndrome. A combination of anti-Ri onconeural antibodies and a particular SOD1 gene mutation, consisting in risk factor, might be in cause in the process of motor neuron death. When in doubt, paraneoplastic cause should be suspected in the differential diagnosis of MND. Immunotherapy treatment may lead to a favorable outcome.


Subject(s)
Antigens, Neoplasm/immunology , Motor Neuron Disease/genetics , Nerve Tissue Proteins/immunology , Paraneoplastic Syndromes/genetics , RNA-Binding Proteins/immunology , Sequence Deletion/genetics , Superoxide Dismutase/genetics , Aged, 80 and over , Animals , Antibodies/blood , Female , Humans , Models, Molecular , Motor Neuron Disease/complications , Neuro-Oncological Ventral Antigen , Paraneoplastic Syndromes/complications , Superoxide Dismutase-1
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