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1.
J Pers Disord ; 23(5): 535-40, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19817633

RESUMO

Although low pre-morbid IQ is an established risk factor for severe mental illness, its association with personality disorder (PD) is unclear. We set out to examine whether there is a prospective association between childhood intelligence and PD in adulthood. Using a population-based prospective cohort study, we linked childhood IQ scores to routinely collected hospital discharge records in adulthood. Lower IQ scores were related to higher risk of being hospitalized with a PD across the full range of IQ scores, (odds ratio per one SD increase in IQ was 0.60; 95% CI: 0.49-0.75; p(trend) = 0.001). Adjusting for potential confounding variables had virtually no impact. We conclude that low childhood IQ predicts hospitalization with PD and may be an important factor in the development of PD.


Assuntos
Inteligência , Transtornos da Personalidade/psicologia , Adolescente , Adulto , Ansiedade/psicologia , Feminino , Hospitalização , Humanos , Testes de Inteligência , Masculino , Pessoa de Meia-Idade , Razão de Chances , Transtornos da Personalidade/epidemiologia , Valor Preditivo dos Testes , Estudos Prospectivos , Fatores de Risco , Suécia/epidemiologia
2.
Dev Psychopathol ; 19(4): 1089-103, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17931436

RESUMO

It is established that reading and reading-related processes are heritable; genes thus play an important role in the foundation of individual differences in reading. In this article, we focus on one facet of reading-comprehension. Comprehension is a higher order cognitive skill that requires many other cognitive processes for it to unfold completely and successfully. One such process is executive functioning, which has been associated with genetic variation in the catechol-O-methyltransferase (COMT) gene. Genotypes and haplotypes of four single nucleotide polymorphisms in COMT were investigated in 179 incarcerated adolescent delinquents. Four hierarchical logistic regression models predicting the presence/absence of comprehension difficulties were fitted to the data; genetic variation in COMT and the presence/absence of maternal rejection were investigated as main effects and as effects acting interactively. Three out of four interaction terms were found to be important predictors of individual differences in comprehension. These findings were supported by the results of the haplotype analyses, in which the four investigated polymorphisms were considered simultaneously.


Assuntos
Catecol O-Metiltransferase/genética , Compreensão , Dislexia/genética , Dislexia/psicologia , Predisposição Genética para Doença/genética , Genótipo , Individualidade , Leitura , Meio Social , Adolescente , Haplótipos , Humanos , Delinquência Juvenil/psicologia , Masculino , Polimorfismo de Nucleotídeo Único/genética , Análise de Regressão , Rejeição em Psicologia , Federação Russa
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