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1.
Mol Psychiatry ; 17(3): 337-49, 2012 Mar.
Article in English | MEDLINE | ID: mdl-21173776

ABSTRACT

Personality can be thought of as a set of characteristics that influence people's thoughts, feelings and behavior across a variety of settings. Variation in personality is predictive of many outcomes in life, including mental health. Here we report on a meta-analysis of genome-wide association (GWA) data for personality in 10 discovery samples (17,375 adults) and five in silico replication samples (3294 adults). All participants were of European ancestry. Personality scores for Neuroticism, Extraversion, Openness to Experience, Agreeableness and Conscientiousness were based on the NEO Five-Factor Inventory. Genotype data of ≈ 2.4M single-nucleotide polymorphisms (SNPs; directly typed and imputed using HapMap data) were available. In the discovery samples, classical association analyses were performed under an additive model followed by meta-analysis using the weighted inverse variance method. Results showed genome-wide significance for Openness to Experience near the RASA1 gene on 5q14.3 (rs1477268 and rs2032794, P=2.8 × 10(-8) and 3.1 × 10(-8)) and for Conscientiousness in the brain-expressed KATNAL2 gene on 18q21.1 (rs2576037, P=4.9 × 10(-8)). We further conducted a gene-based test that confirmed the association of KATNAL2 to Conscientiousness. In silico replication did not, however, show significant associations of the top SNPs with Openness and Conscientiousness, although the direction of effect of the KATNAL2 SNP on Conscientiousness was consistent in all replication samples. Larger scale GWA studies and alternative approaches are required for confirmation of KATNAL2 as a novel gene affecting Conscientiousness.


Subject(s)
Genome-Wide Association Study , Personality/genetics , Adenosine Triphosphatases/genetics , Adenosine Triphosphatases/physiology , Adult , Aged , Australia , Chromosomes, Human/genetics , Computer Simulation , Europe/ethnology , Exploratory Behavior , Female , Genotype , Humans , Katanin , Male , Middle Aged , Models, Psychological , Personality Inventory , Phenotype , Polymorphism, Single Nucleotide , Sampling Studies , United States , White People/genetics
2.
Transl Psychiatry ; 1: e49, 2011 Oct 18.
Article in English | MEDLINE | ID: mdl-22833195

ABSTRACT

The tendency to seek stimulating activities and intense sensations define excitement-seeking, a personality trait akin to some aspects of sensation-seeking. This trait is a central feature of extraversion and is a component of the multifaceted impulsivity construct. Those who score high on measures of excitement-seeking are more likely to smoke, use other drugs, gamble, drive recklessly, have unsafe/unprotected sex and engage in other risky behaviors of clinical and social relevance. To identify common genetic variants associated with the Excitement-Seeking scale of the Revised NEO Personality Inventory, we performed genome-wide association studies in six samples of European ancestry (N=7860), and combined the results in a meta-analysis. We identified a genome-wide significant association between the Excitement-Seeking scale and rs7600563 (P=2 × 10(-8)). This single-nucleotide polymorphism maps within the catenin cadherin-associated protein, alpha 2 (CTNNA2) gene, which encodes for a brain-expressed α-catenin critical for synaptic contact. The effect of rs7600563 was in the same direction in all six samples, but did not replicate in additional samples (N=5105). The results provide insight into the genetics of excitement-seeking and risk-taking, and are relevant to hyperactivity, substance use, antisocial and bipolar disorders.


Subject(s)
Genetic Variation , Genome-Wide Association Study/methods , Psychomotor Agitation/genetics , Psychomotor Agitation/metabolism , alpha Catenin/genetics , Adolescent , Adult , Australia/epidemiology , Baltimore/epidemiology , Estonia/epidemiology , Female , Finland/epidemiology , Germany/epidemiology , Humans , Italy/epidemiology , Longitudinal Studies , Male , Middle Aged , Netherlands/epidemiology , Polymorphism, Single Nucleotide/genetics , Psychomotor Agitation/classification , Young Adult
3.
Transl Psychiatry ; 1: e50, 2011 Oct 18.
Article in English | MEDLINE | ID: mdl-22833196

ABSTRACT

The relationship between major depressive disorder (MDD) and bipolar disorder (BD) remains controversial. Previous research has reported differences and similarities in risk factors for MDD and BD, such as predisposing personality traits. For example, high neuroticism is related to both disorders, whereas openness to experience is specific for BD. This study examined the genetic association between personality and MDD and BD by applying polygenic scores for neuroticism, extraversion, openness to experience, agreeableness and conscientiousness to both disorders. Polygenic scores reflect the weighted sum of multiple single-nucleotide polymorphism alleles associated with the trait for an individual and were based on a meta-analysis of genome-wide association studies for personality traits including 13,835 subjects. Polygenic scores were tested for MDD in the combined Genetic Association Information Network (GAIN-MDD) and MDD2000+ samples (N=8921) and for BD in the combined Systematic Treatment Enhancement Program for Bipolar Disorder and Wellcome Trust Case-Control Consortium samples (N=6329) using logistic regression analyses. At the phenotypic level, personality dimensions were associated with MDD and BD. Polygenic neuroticism scores were significantly positively associated with MDD, whereas polygenic extraversion scores were significantly positively associated with BD. The explained variance of MDD and BD, ∼0.1%, was highly comparable to the variance explained by the polygenic personality scores in the corresponding personality traits themselves (between 0.1 and 0.4%). This indicates that the proportions of variance explained in mood disorders are at the upper limit of what could have been expected. This study suggests shared genetic risk factors for neuroticism and MDD on the one hand and for extraversion and BD on the other.


Subject(s)
Bipolar Disorder/genetics , Depressive Disorder, Major/genetics , Multifactorial Inheritance/genetics , Adult , Aged , Female , Genome-Wide Association Study , Humans , Male , Meta-Analysis as Topic , Middle Aged , Personality/genetics , Personality Inventory , Registries
4.
J Pers Assess ; 70(1): 109-24, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9615427

ABSTRACT

The Self-Consciousness Scale (SCS), developed by Fenigstein, Scheier, and Buss (1975), was adapted to the Estonian language. In general, the results supported the 3-factor structure of the SCS. However, many items in the subscales did not load as expected. A 26-item modified scale, the Estonian SCS (ESCS), is presented. A joint factor analysis of the ESCS and the NEO Personality Inventory (NEO-PI) scales led to a 5-factor solution, where all the factors that emerged were identified as the Big Five personality dimensions, the ESCS subscales loading most significantly on 3 of these factors: Neuroticism (N), Extraversion (E), and Openness to Experience (O). Correlation analysis revealed a pattern of correlations, characterized by the strongest associations between Social Anxiety and E (r = -.77), Public Self-Consciousness (PubSC) and N (r = .40), and Private Self-Consciousness (PrivSC) and O (r = .34), which quite well corresponds to the pattern of correlations that was reported for the original versions of the SCS and the NEO-PI (Zuckerman, Kuhlman, Joireman, Teta, & Kraft, 1993). We can conclude that all the SCS subscales can be sufficiently well interpreted in terms of the Big Five model of personality dimensions--PrivSC and PubSC appear to describe some variations of the Big Five themes that are not fully elaborated by the NEO-PI rather than being completely independent domains of individual differences.


Subject(s)
Personality Inventory , Psychometrics , Social Perception , Translating , Adult , Estonia , Factor Analysis, Statistical , Female , Humans , Male , Models, Psychological , Reproducibility of Results
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