Chrysoula Zouraraki
University of Crete
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Featured researches published by Chrysoula Zouraraki.
Biological Psychiatry | 2016
Panos Roussos; Stella G. Giakoumaki; Chrysoula Zouraraki; John F. Fullard; Vasiliki-Eirini Karagiorga; Eva-Maria Tsapakis; Zoe Petraki; Larry J. Siever; Todd Lencz; Anil K. Malhotra; Cleanthe Spanaki; Panos Bitsios
BACKGROUND Prepulse inhibition (PPI) of the startle reflex has been suggested as a candidate endophenotype for schizophrenia research, as it shows high heritability and has been found deficient in schizophrenia spectrum disorders. The objectives of the study were to 1) identify common genetic variants associated with baseline startle and PPI; 2) estimate the single nucleotide polymorphism heritability; and 3) examine the relationship of polygenic score for schizophrenia with baseline startle and PPI. METHODS A cohort of healthy young male subjects (n = 1493) originating from the Learning on Genetics of Schizophrenia Spectrum project was assessed for baseline startle and PPI. The most recent genome-wide association study in schizophrenia from the Psychiatric Genomics Consortium 2 was used to calculate polygenic scores. RESULTS Eleven loci showed suggestive association (p < 10(-6)) with baseline startle and PPI in the discovery cohort. Additional genotyping in a replication cohort identified genome-wide significant association at two loci (rs61810702 and rs4718984). These loci were co-localized with expression quantitative trait loci associated with gene expression of nerve growth factor (NGF) and calneuron 1 (CALN1) genes. Estimation of the genetic and environmental contributions to baseline startle and PPI showed a substantial single nucleotide polymorphism heritability for 120-ms PPI stimuli. Increased polygenic risk score for schizophrenia was associated with reduced PPI. CONCLUSIONS Common genetic variation has an important role in the etiology of schizophrenia and PPI impairments. Overall, these data support the idea that PPI is a valid endophenotype that can be used to explore the genetic architecture of schizophrenia.
European Psychiatry | 2015
Emmanouil Pasparakis; Erasmia Koiliari; Chrysoula Zouraraki; E.M. Tsapakis; Panos Roussos; Stella G. Giakoumaki; Panos Bitsios
BACKGROUND The CACNA1C rs1006737 risk A allele has been associated with affective psychoses and functional studies indicate that it is associated with increased hippocampal/amygdala activity during emotional face-processing. Here we studied the impact of the risk A allele on affective startle modulation. METHODS Hundred and ninety-four healthy males stratified for their CACNA1C rs1006737 genotype (GG:111, GA:67, AA:16) were presented with 18 pleasant, 18 unpleasant and 18 neutral pictures with acoustic probes (104 dB) occurring during 12 pictures in each affective category. Baseline startle was assessed during blank screens. State mood was self-rated on arrival, pre- and post-test and the emotional valence and arousal of affective pictures at post-test. RESULTS Relative to the other genotypes, risk A allele homozygotes presented with higher anxiety/negative affect at pre-test, reduced and exaggerated physiological responses to the pleasant and negative pictures respectively, negative affect with reduced arousal at post-test and rated the affective pictures as less arousing and inconsistently to their physiological responses (all P<0.05). Sustained contextual negative mood predicted reduced baseline and affective startle reactivity in the AA group. CONCLUSIONS Healthy homozygous males for the risk A allele appear to have marked contextual sensitivity, affective reactivity akin to anxiety and depression and inefficient emotional appraisal. Our findings provide phenotypic detail of the CACNA1C AA genotype in non-symptomatic individuals, which suggest primary effects in emotional circuitry, consistent with previously documented alterations in hippocampal/amygdala processing.
Journal of Clinical and Experimental Neuropsychology | 2016
Leda Karagiannopoulou; Penny Karamaouna; Chrysoula Zouraraki; Panos Roussos; Panos Bitsios; Stella G. Giakoumaki
ABSTRACT Introduction: Studies assessing the effects of schizotypal dimensions (i.e., positive, negative, and disorganized) on cognitive functions have yielded mixed findings. In the present study, we administered an extensive battery of cognitive tasks to a community sample and defined the schizotypal dimensions according to a more analytical four-factor model, whereby positive schizotypy is further divided into cognitive–perceptual and paranoid. Method: Two hundred healthy community participants were assessed for schizotypy with the Schizotypal Personality Questionnaire; assessment of cognitive functions included set shifting, working memory, processing speed, verbal fluency, attention switching, planning/problem solving, strategy formation, and abstract reasoning. Associations between cognitive tasks and schizotypy were examined with hierarchical multiple linear regressions. We also divided our subjects into groups based on whether or not their scores in the negative, positive, and cognitive–perceptual factors fell in the upper 10% of the scores of a large community normative sample in Greece and examined between-group differences. Results: Applying both dimensional and categorical approaches, we showed that (a) attention-switching impairment is a “core” deficit of both negative and paranoid schizotypy, (b) impaired working memory and set shifting are associated mainly with negative and to a lesser extent paranoid schizotypy, (c) paranoid schizotypy is associated with reduced performance in tasks requiring intact frontotemporal connectivity, and (d) cognitive–perceptual and disorganized schizotypy are not associated with any cognitive functions. Conclusions: Our findings further support the more analytical four-factor categorization of schizotypy and suggest that the discrepancies in the findings so far might be due to a more “generalized” definition of the schizotypal dimensions. They also add further in the early formulation of the profile of the high-schizotypal individuals seeking psychiatric help so that their overall management is directed towards a more targeted approach.
PeerJ | 2016
Stella G. Giakoumaki; Leda Karagiannopoulou; Sándor Rózsa; Chrysoula Zouraraki; Penny Karamaouna; C. Robert Cloninger
Background. The revised Temperament and Character Inventory (TCI-R) measures Cloninger’s psychobiological model of personality. The average effects of individual temperament and character traits have been associated with schizotypy and with impaired regulation of affect and cognition. We extended prior research by testing predictions about the association of specific multidimensional configurations of temperament and character traits on schizotypy, affect balance, and self-perceived cognitive functioning. Method. A well-educated sample of native Greeks (N = 483), completed a new Greek translation of the TCI-R, as well as the Schizotypal Personality Questionnaire (SPQ), the Positive/Negative Affect Schedule (PANAS) and the Cognitive Failures Questionnaire (CFQ). The factor structure of the TCI-R was examined with exploratory and confirmatory tests. Associations between reported measures were examined with correlational and regression analyses. Results. The TCI-R had good psychometric properties as expected from studies in other countries. As predicted, specific configurations of temperament and character were associated with schizotypy, negative affect balance, and cognitive lapses. The “Borderline/Explosive temperament” (high Novelty Seeking, high Harm Avoidance, low Reward Dependence), “Schizotypal/Disorganized character” (low Self-directedness, low Cooperativeness, high Self-transcendence), and “Low Ego Strength/Fragile” profile (high Harm Avoidance, low Persistence, low Self-Directedness) were each strongly associated with higher stereotypy, negative affect balance (low positive affect and high negative affect), and subjective cognitive lapses compared to their contrast groups. Discussion. Multidimensional TCI profiles are strongly related to individual differences in schizotypy and self-reported regulation of affect and cognition. The Greek translation of the TCI-R is psychometrically sound and useful for clinical assessment and research.
Comprehensive Psychiatry | 2016
Chrysoula Zouraraki; Ioannis Tsaousis; Penny Karamaouna; Leda Karagiannopoulou; Panos Roussos; Panos Bitsios; Stella G. Giakoumaki
BACKGROUND Increased schizotypal traits are observed in a percentage of the general population and in the schizophrenia-spectrum and have been associated with impairments in working memory. In this study we examined the effects of four schizotypal dimensions [Negative (NegS), Paranoid (ParS), Cognitive-Perceptual (CPS), Disorganized (DiS)] on executive working memory (EWM), as mediated by set-shifting, planning and control inhibition. We also examined whether these associations are moderated by family-history of psychosis. METHODS Our sample consisted of 110 unaffected first-degree relatives of schizophrenia-spectrum patients and 120 control individuals. Schizotypy was assessed with the Schizotypal Personality Questionnaire. Participants were also tested with the Letter-Number Sequencing, Wisconsin Card Sorting, Stroop Color-Word and Stockings of Cambridge tasks. The effects of set-shifting, control inhibition and planning on the relationship between schizotypy and EWM were examined with mediation analyses. Moderated-mediation analyses examined potential moderating effects of group membership (unaffected relative/community participant). RESULTS All mediators were significant in the relationship between NegS and EWM. The effects of ParS were mediated only by set-shifting and planning. Planning and control inhibition were the only significant mediators on the effects of CPS and DiS on EWM, respectively. The moderated-mediation analyses revealed that these findings apply only in the community group. CONCLUSIONS We found that the effects of different schizotypal dimensions on EWM are mediated by other cognitive processes in individuals without personal/family history of psychosis. This is probably due to either more severe impairments in the cognitive processes of the relatives or restrictions in our sample and study-design.
Comprehensive Psychiatry | 2015
Ioannis Tsaousis; Chrysoula Zouraraki; Penny Karamaouna; Leda Karagiannopoulou; Stella G. Giakoumaki
European Psychiatry | 2013
Stella G. Giakoumaki; Panos Roussos; Chrysoula Zouraraki; E. Spanoudakis; Maria Mavrikaki; Eva-Maria Tsapakis; Panos Bitsios
Biological Psychology | 2013
Stella G. Giakoumaki; Panos Roussos; Eva-Maria Tsapakis; Erasmia Koiliari; Emmanouil Pasparakis; Chrysoula Zouraraki; Panos Bitsios
Archives of Clinical Neuropsychology | 2017
Chrysoula Zouraraki; Penny Karamaouna; Leda Karagiannopoulou; Stella G. Giakoumaki
European Psychiatry | 2015
Panos Bitsios; Leda Karagiannopoulou; Penny Karamaouna; Chrysoula Zouraraki; Panos Roussos; Stella G. Giakoumaki