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1.
Eur Psychiatry ; 47: 9-18, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-29096131

RESUMO

BACKGROUND: Urbanicity, immigration and winter-birth are stable epidemiological risk factors for schizophrenia, but their relationship to schizotypy is unknown. This is a first examination of the association of these epidemiological risk factors with positive schizotypy, in nonclinical adolescents, controlling for a range of potential and known confounders. METHODS: We collected socio-demographics, life-style, family and school circumstances, positive schizotypy dimensions and other personality traits from 445 high school pupils (192 males, 158 immigrants) from 9 municipalities in Athens and Heraklion, Greece, which covered a range of host population and migrant densities. Using multivariate hierarchical linear regressions models, we estimated the association of schizotypy dimensions with: (1) demographics of a priori interest (winter-birth, immigrant status, urban characteristics), including family financial and mental health status; (2) factors resulting from principal component analysis (PCA) of the demographic and personal data; (3) factors resulting from PCA of the personality questionnaires. RESULTS: Adolescent women scored higher on schizotypy than men. High anxiety/neuroticism was the most consistent and significant predictor of all schizotypy dimensions in both sexes. In the fully adjusted models, urbanicity predicted magical thinking and unusual experiences in women, while winter-birth and immigration predicted paranoid ideation and unusual experiences respectively in men. CONCLUSIONS: These results support the continuum hypothesis and offer potential insights in the nature of risk conferred by winter-birth, urbanicity and immigration and the nature of important sex differences. Controlling for a wide range of potential confounding factors increases the robustness of these results and confidence that these were not spurious associations.


Assuntos
Emigrantes e Imigrantes/estatística & dados numéricos , Transtorno da Personalidade Esquizotípica/epidemiologia , Transtorno da Personalidade Esquizotípica/etiologia , Estações do Ano , População Urbana/estatística & dados numéricos , Adolescente , Feminino , Grécia/epidemiologia , Humanos , Modelos Lineares , Masculino , Personalidade , Análise de Componente Principal , Psicometria , Fatores de Risco , Inquéritos e Questionários , Adulto Jovem
2.
Eur Psychiatry ; 30(4): 492-8, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25841664

RESUMO

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.


Assuntos
Canais de Cálcio Tipo L/genética , Transtornos do Humor/genética , Polimorfismo de Nucleotídeo Único/genética , Reflexo de Sobressalto/genética , Adulto , Alelos , Genótipo , Humanos , Masculino , Testes Neuropsicológicos , Personalidade/genética , Fatores de Risco , Adulto Jovem
3.
Eur Psychiatry ; 28(4): 254-60, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23062835

RESUMO

Part of the variation in personality characteristics has been attributed to the child-parent interaction and sub-optimal parenting has been associated with psychiatric morbidity. In the present study, an extensive battery of personality scales (Trait Anxiety Inventory, Behavioural Inhibition/Activation System questionnaire, Eysenck Personality Questionnaire-Revised, Temperament and Character Inventory, Schizotypal Traits Questionnaire, Toronto Alexithymia Scale) and the Parental Bonding Instrument (PBI) were administered in 324 adult healthy males to elucidate the effects of parenting on personality configuration. Personality variables were analysed using Principal Component Analysis (PCA) and the factors "Schizotypy", "Anxiety", "Behavioural activation", "Novelty seeking" and "Reward dependence" were extracted. Associations between personality factors with PBI "care" and "overprotection" scores were examined with regression analyses. Subjects were divided into "parental style" groups and personality factors were subjected to categorical analyses. "Schizotypy" and "Anxiety" were significantly predicted by high maternal overprotection and low paternal care. In addition, the Affectionless control group (low care/high overprotection) had higher "Schizotypy" and "Anxiety" compared with the Optimal Parenting group (high care/low overprotection). These results further validate sub-optimal parenting as an important environmental exposure and extend our understanding on the mechanisms by which it increases risk for psychiatric morbidity.


Assuntos
Transtornos de Ansiedade/etiologia , Ansiedade/etiologia , Relações Pais-Filho , Poder Familiar/psicologia , Personalidade , Transtorno da Personalidade Esquizotípica/etiologia , Adolescente , Adulto , Ansiedade/psicologia , Transtornos de Ansiedade/psicologia , Humanos , Masculino , Apego ao Objeto , Pais/psicologia , Inventário de Personalidade , Transtorno da Personalidade Esquizotípica/psicologia , Inquéritos e Questionários
4.
Psychol Med ; 38(11): 1651-8, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18261249

RESUMO

BACKGROUND: Recent evidence suggests that dopamine (DA) agonist-induced disruption of prepulse inhibition (PPI) depends on basal PPI values, in a manner that suggests an inverted U-shaped relationship between PPI and prefrontal DA levels. This is the first study to examine possible genetic determinants of PPI and the catechol O-methyltransferase (COMT) Val158Met polymorphism, the main catabolic pathway of released DA in the prefrontal cortex (PFC). METHOD: PPI was measured in 93 healthy males presented with 75-dB and 85-dB prepulses at 60-ms and 120-ms prepulse-pulse intervals. Subjects were grouped according to their COMT status into a Val/Val, a Val/Met and a Met/Met group. RESULTS: ANOVAs showed that at all prepulse and interval conditions, Val/Val individuals had the lowest PPI, Met/Met the highest, and Val/Met were intermediate. CONCLUSIONS: These results suggest that PPI is regulated by DA neurotransmission in the PFC and its levels depend on the COMT Val158Met gene polymorphism. These findings enhance the value of the PPI paradigm in examining individual variability of early information processing in healthy subjects and psychiatric disorders associated with changes in PFC DA activity and attentional deficits such as schizophrenia.


Assuntos
Alelos , Catecol O-Metiltransferase/genética , Inibição Neural/genética , Polimorfismo de Fragmento de Restrição/genética , Reflexo de Sobressalto/genética , Estimulação Acústica , Adolescente , Adulto , Dopamina/metabolismo , Genótipo , Humanos , Masculino , Reação em Cadeia da Polimerase , Córtex Pré-Frontal/fisiologia , Valores de Referência , Reflexo de Sobressalto/fisiologia , Adulto Jovem
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