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1.
Arch Womens Ment Health ; 20(5): 663-672, 2017 10.
Article in English | MEDLINE | ID: mdl-28634716

ABSTRACT

The objective of this study was to explore how maternal mood during pregnancy, i.e., general anxiety, pregnancy-specific anxiety, and depression predicted parenting stress 3 months after giving birth, thereby shaping the child's early postnatal environmental circumstances. To this end, data were used from 1073 women participating in the Dutch longitudinal cohort Generations2, which studies first-time pregnant mothers during pregnancy and across the transition to parenthood. Women filled out the State Trait Anxiety Inventory (STAI), Pregnancy-Related Anxiety Questionnaire-revised (PRAQ-R), and Beck Depression Index (BDI) three times during pregnancy: at 12, 22, and 32 weeks gestational age. Three months postpartum, a parenting stress questionnaire was filled out yielding seven different parenting constructs. Latent scores were computed for each of the repeatedly measured maternal mood variables with Mplus and parenting stress constructs were simultaneously regressed on these latent scores. Results showed that trait anxiety and pregnancy-specific anxiety were uniquely related to almost all parenting stress constructs, taking depression into account. Early prevention and intervention to reduce maternal anxiety in pregnancy could hold the key for a more advantageous trajectory of early postnatal parenting.


Subject(s)
Anxiety/epidemiology , Anxiety/psychology , Depression, Postpartum/epidemiology , Depression/epidemiology , Parenting/psychology , Parents/psychology , Pregnancy Complications/psychology , Stress, Psychological/epidemiology , Stress, Psychological/etiology , Adult , Anxiety/diagnosis , Anxiety Disorders , Depression/diagnosis , Depression/psychology , Depression, Postpartum/diagnosis , Female , Humans , Longitudinal Studies , Netherlands/epidemiology , Personality Inventory , Postpartum Period/psychology , Pregnancy , Pregnancy Complications/diagnosis , Pregnancy Complications/drug therapy , Risk Factors , Stress, Psychological/diagnosis , Stress, Psychological/psychology , Surveys and Questionnaires , Young Adult
2.
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
3.
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
4.
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
5.
Diabetologia ; 52(12): 2570-7, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19802603

ABSTRACT

AIMS/HYPOTHESIS: The aim of the present study was to estimate the heritability of the beta cell insulin response to glucose and to glucose combined with glucagon-like peptide-1 (GLP-1) or with GLP-1 plus arginine. METHODS: This was a twin-family study that included 54 families from the Netherlands Twin Register. The participants were healthy twin pairs and their siblings of the same sex, aged 20 to 50 years. Insulin response of the beta cell was assessed by a modified hyperglycaemic clamp with additional GLP-1 and arginine. Insulin sensitivity index (ISI) was assessed by the euglycaemic-hyperinsulinaemic clamp. Multivariate structural equation modelling was used to obtain heritabilities and the genetic factors underlying individual differences in BMI, ISI and secretory responses of the beta cell. RESULTS: The heritability of insulin levels in response to glucose was 52% and 77% for the first and second phase, respectively, 53% in response to glucose + GLP-1 and 80% in response to an additional arginine bolus. Insulin responses to the administration of glucose, glucose + GLP-1 and glucose + GLP-1 + arginine were highly correlated (0.62< r <0.79). Heritability of BMI and ISI was 74% and 60% respectively. The genetic factors that influenced BMI and ISI explained about half of the heritability of insulin levels in response to the three secretagogues. The other half was due to genetic factors specific to the beta cell. CONCLUSIONS/INTERPRETATION: In healthy adults, genetic factors explain most of the individual differences in the secretory capacity of the beta cell. These genetic influences are partly independent from the genes that influence BMI and ISI.


Subject(s)
Insulin-Secreting Cells/metabolism , Insulin/metabolism , Adult , Body Mass Index , Body Weight , Glucagon-Like Peptide 1/pharmacology , Glucagon-Like Peptide-1 Receptor , Glucose Clamp Technique , Humans , Hyperinsulinism , Insulin/genetics , Insulin/pharmacology , Insulin Secretion , Insulin-Secreting Cells/drug effects , Kinetics , Middle Aged , Multivariate Analysis , Receptors, Glucagon/physiology , Young Adult
6.
Eur J Epidemiol ; 22(1): 27-32, 2007.
Article in English | MEDLINE | ID: mdl-17195050

ABSTRACT

The purpose of this study is to investigate whether there is an association between exercise participation and self-rated health and whether this association can be explained by common genes and/or common environmental influences. In a sample of 5,140 Dutch adult twins and their non-twin siblings from 2,831 families, exercise participation (sedentaries, light or moderate, vigorous exercisers) and self-rated health were assessed by survey. To investigate the etiology of the association, bivariate genetic models using structural equation modeling were applied to the data. The correlation between exercise participation and self-rated health is significant but modest (r = 0.20). Exercise participation and self-rated health are both heritable (around 50% of the variance of both phenotypes is explained by genetic factors). The genetic factors influencing exercise participation and self-rated health partially overlap (r = 0.36) and this overlap fully explains their phenotypic correlation. We conclude that the association between exercise and self-rated health can be explained by genes predisposing to both exercise participation and self-rated health. These genes may directly influence both phenotypes (pleiotropy). Alternatively, genes that affect exercise or self-rated health may indirectly influence the other phenotype through a causal relationship. We propose that identification of the genes that cause differences in exercise behavior will help resolve the issue of causality.


Subject(s)
Exercise , Genetic Variation , Health Status , Siblings , Twins/genetics , Adolescent , Adult , Environment , Female , Humans , Male , Middle Aged , Models, Statistical , Netherlands
7.
Prev Med ; 44(2): 148-52, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17059845

ABSTRACT

OBJECTIVE: We investigated the association between leisure time exercise participation and well-being (i.e., life satisfaction and happiness) and examined the causality underlying this association. METHOD: The association between exercise participation and well-being was assessed in around 8000 subjects, (age range 18-65 years) from The Netherlands Twin Registry (NTR). Causality was tested with the co-twin control method in 162 monozygotic (MZ) twin pairs, 174 dizygotic (DZ) twin and sibling pairs, and 2842 unrelated individuals. RESULTS: Exercisers were more satisfied with their life and happier than non-exercisers at all ages. The odds ratio for life satisfaction given exercise participation was significantly higher than unity in unrelated pairs, and a trend was visible in DZ pairs. In MZ pairs, the odds ratio was close to unity. The pattern of odds ratios for happiness given exercise participation was similar. CONCLUSION: Exercise participation is associated with higher levels of life satisfaction and happiness. This association is non-causal and appears to be mediated by genetic factors that influence both exercise behavior and well-being.


Subject(s)
Adaptation, Psychological , Exercise/psychology , Happiness , Leisure Activities , Mental Health , Personal Satisfaction , Twins/psychology , Adolescent , Adult , Aged , Exercise/physiology , Female , Humans , Male , Middle Aged , Netherlands , Prospective Studies , Registries , Twins/physiology , Twins, Dizygotic , Twins, Monozygotic
8.
Prev Med ; 42(4): 273-9, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16439008

ABSTRACT

OBJECTIVES: To examine whether regular exercise is associated with anxiety, depression and personality in a large population-based sample as a function of gender and age. METHODS: The sample consisted of adolescent and adult twins and their families (N=19,288) who participated in the study on lifestyle and health from The Netherlands Twin Registry (1991-2002). Exercise participation, anxiety, depression and personality were assessed with self-report questionnaires. RESULTS: The overall prevalence of exercise participation (with a minimum of 60 min weekly at 4 METs (Metabolic Energy Expenditure Index)) in our sample was 51.4%. Exercise participation strongly declined with age from about 70% in young adolescents to 30% in older adults. Among adolescents, males exercised more, whereas, among older adults, females exercised more. Exercisers were on average less anxious (-0.18 SD), depressed (-0.29 SD) and neurotic (-0.14 SD), more extraverted (+0.32 SD) and were higher in dimensions of sensation seeking (from+0.25 SD to+0.47 SD) than non-exercisers. These differences were modest in size, but very consistent across gender and age. CONCLUSIONS: This study corroborates and extends previous findings: regular exercise is cross-sectionally associated with lower neuroticism, anxiety and depression and higher extraversion and sensation seeking in the population.


Subject(s)
Anxiety/epidemiology , Depression/epidemiology , Exercise/psychology , Mental Health , Neurotic Disorders/epidemiology , Personality , Adolescent , Adult , Anxiety/prevention & control , Cross-Sectional Studies , Depression/prevention & control , Female , Humans , Life Style , Male , Middle Aged , Netherlands/epidemiology , Neurotic Disorders/prevention & control , Prevalence , Registries , Surveys and Questionnaires , Twins
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