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Article Associative learning, acquired equivalence, and flexible generalization of knowledge in mild Alzheimer disease. 2009
Bódi N, Csibri E, Myers CE, Gluck MA, Kéri S. · Department of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary. · Cogn Behav Neurol. · Pubmed #19506424 No free full text.
Abstract: BACKGROUND: Acquired equivalence is a phenomenon in which prior training to treat 2 stimuli as equivalent increases generalization between them. Previous studies demonstrated that the hippocampal complex might play an important role in acquired equivalence associative learning. In this study, we tested the possibility that acquired equivalence learning is a sensitive marker of mild Alzheimer disease (AD). METHODS: In the associative learning test, antecedent stimuli were cartoon faces and consequent stimuli were different colored cartoon fishes. Each cartoon character had some pet fish and the task was to learn these face-fish associations using feedback provided after each decision. In the transfer phase, knowledge about face-fish pairs had to be generalized to new associations. RESULTS: AD patients exhibited mild impairments in the training phase, whereas they were profoundly impaired on the acquired equivalence test. Associative knowledge could not be transferred to a more flexible retrieval condition. CONCLUSIONS: These results suggest that acquired equivalence learning is specifically impaired in early AD, which may indicate the pathology of the hippocampal complex.
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Article Quantitative EEG in early Alzheimer's disease patients - power spectrum and complexity features. 2008
Czigler B, Csikós D, Hidasi Z, Anna Gaál Z, Csibri E, Kiss E, Salacz P, Molnár M. · Institute for Psychology, Hungarian Academy of Sciences, Budapest, Hungary. · Int J Psychophysiol. · Pubmed #18093675 No free full text.
Abstract: The goal of this study was to investigate the EEG signs of early stage Alzheimer's disease (AD) by conventional analyses and by methods quantifying linear and nonlinear EEG-complexity. The EEG was recorded in 12 mild AD patients and in an age-matched healthy control group (24 subjects) in both eyes open and eyes closed conditions. Frequency spectra, Omega-complexity and Synchronization likelihood were calculated on the data. In the patients a significant decrease of the relative alpha and increase of the theta power were found. Remarkably increased Omega-complexity and lower Synchronization likelihood were observed in AD in the 0.5-25 Hz frequency ranges. It is concluded that both spectral- and EEG-complexity changes can be found already in the early stage of AD in a wide frequency range. Application of conventional EEG analysis methods in combination with quantification of EEG-complexity may improve the chances of early diagnosis of AD.
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Article Changes of EEG spectra and coherence following performance in a cognitive task in Alzheimer's disease. 2007
Hidasi Z, Czigler B, Salacz P, Csibri E, Molnár M. · Department of Psychiatry and Psychotherapy, General Medical Faculty, Semmelweis University, Budapest, Hungary. · Int J Psychophysiol. · Pubmed #17586077 No free full text.
Abstract: Electroencephalographic measures combined with cognitive tasks are widely used for the assessment of cognitive and pathophysiological changes in Alzheimer's disease (AD). Instead of the analysis of EEG data obtained during the performance of the task, in this study data recorded in the immediate after-task period were analyzed. It was expected that this period would correspond to the electrophysiological consequences of the cognitive effort. Data of 14 patients with AD (MMS score: 16-24) were compared to that of 10 healthy control subjects. Reverse counting of a fix duration was used as a cognitive task. Changes of relative frequency spectra, and those of inter-and intrahemispheric coherence were analyzed. Relative theta power was significantly higher in AD patients compared to the controls both before and after the task. The performance of the task resulted in an increase of the relative alpha2 band in the AD group, whereas it slightly decreased in the control group. The most prominent coherence differences between AD and controls were found in the alpha1 band, especially for long-range coherence values. Coherence in this frequency band increased in the control group following the task, not seen in the AD group. We conclude that EEG parameters calculated from epochs following the completion of a cognitive task clearly differentiates patients with AD from normal controls. The electrophysiological changes found in AD may correspond to the decrease of functional connectivity of cortical areas and to the malfunctioning of the networks engaged in the cognitive task investigated.
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Article [Quantitative EEG analysis in Alzheimer's disease: spectral, coherence and complexity parameters] 2006
Czigler B, Csikós D, Gaál AZ, Csibri E, Kiss E, Hidasi Z, Salacz P, Molnár M. · MTA Pszichológiai Kutatóintézet, Budapest, Hungary. · Psychiatr Hung. · Pubmed #17170472 No free full text.
Abstract: In our study we examined the linear and non-linear characteristics of EEG signals derived from patients with Alzheimer's disease (AD) with the future aim of developing a widely available method for monitoring therapy and the progression of the disease or to be used even for the purposes of differential diagnosis. EEG was recorded with eyes closed and eyes open conditions ("resting") in a group of patients with early-stage AD and in healthy control subjects matched by age. In addition to the conventional methods of analysis (frequency spectrum, coherence), the so-called complexity measures developed in recent years (Omega-complexity, synchronised probability) have also been determined. By means of frequency spectrum analysis, we managed to detect the slowdown of EEG in the early stage of dementia, a feature that so far has been associated with the later stages of AD. Coherence was reduced in the majority of frequency bands in the patient group; however, this difference could be observed only in some of the leads. Thus, resting EEG coherence is less suitable for separating various stages than the other methods. Complexity features have shown the most robust changes in Alzheimer's disease in our investigation. Besides the reduction in synchronised probability, significantly higher values of Omega-complexity were obtained in the patient group. This may be associated with the impairment of cortical afferentation (cholinergic and monoaminergic) and with the reduction in the number of neurons and synapses. Our methods have proved to be very sensitive to quantify these changes.
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Article The nitric oxide synthase-3 codon 298 polymorphism is not associated with late-onset sporadic Alzheimer's dementia and Lewy body disease in a sample from Hungary. 2003
Kálmán J, Juhász A, Rimanóczy A, Palotás A, Palotás M, Boda K, Márki-Zay J, Csibri E, Janka Z. · Department of Psychiatry, Albert Szent-Györgyi Center for Medical and Pharmaceutical Sciences, Faculty of Medicine, University of Szeged, Hungary. · Psychiatr Genet. · Pubmed #14639046 No free full text.
Abstract: An association study was performed between apolipoprotein E (apoE) polymorphism and the common structural polymorphism Glu/Asp at codon 298 of the nitric oxide synthase (NOS3) gene in late-onset sporadic Alzheimer's dementia probands (LOAD), diffuse Lewy body dementia cases (DLBD) and controls in a Hungarian sample. The frequency of individuals who carried the apoE epsilon4 allele was significantly more common in both dementia groups (LOAD, 20%; DLBD, 27%; control, 8%; control versus DLBD, chi2=13.264, degrees of freedom=2, P<0.001; control versus LOAD, chi2=6.628, degrees of freedom=2, P<0.036). However, there were no significant differences in the NOS3 genotype and allele distributions between the LOAD, DLBD and control groups. The apoE status has been found to be independent from the NOS3 codon 298 polymorphism in the examined cohort. Despite the facts that NOS3 is associated with neuritic sprouting, and aberrant neuronal and glial expression of the same molecule has been found in neurodegenerative diseases, it is unlikely that the polymorphism Glu/Asp of the NOS3 gene is involved in the development of LOAD and DLBD.
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