Importance of shared genes and shared environments for symptoms of depression in older adults.

The Center for Epidemiologic Studies-Depression scale was administered to 68 identical and 161 fraternal twin pairs reared apart and 114 identical and 138 fraternal pairs reared together to ascertain relative genetic and environmental contributions to individual differences in self-reported depressive symptoms. Intraclass correlations and model fitting indicated that genetic influences explained 16% of the variance in total depression scores and 19% for the Psychomotor Retardation and Somatic Complaints subscale, but heritability was minimal for the Depressed Mood and Well-Being subscales. Influence of family rearing context played a substantial role in explaining twin similarity, whereas unique life experiences accounted for the greatest proportion of variance. Significant age group differences were observed, with heritability greater in twins of 60 years of age or older than in twins under 60, especially for Psychomotor Retardation.     

Monozygotic twins with Asperger syndrome: differences in behaviour reflect variations in brain structure and function

A pair of monozygotic twins discordant for symptoms of Asperger syndrome was evaluated at the age of 13.45 years using psychometric, morphometric, behavioural, and functional imaging methods. The lower-functioning twin had a smaller brain overall, a smaller right cerebellum, and a disproportionately large left frontal lobe, and manifested almost no differential activation between distractors of high and low-congruence with target visual stimuli. The higher-functioning twin manifested a typically autistic pattern of anterior deactivation and posterior hyperactivation in response to incongruent distractors, overlaid with a typically normal pattern of activation of superior frontal cortex. The morphometric results are consistent with known correlations between brain structure and behaviour in autism, and the physiological results suggest correspondences between structure and function.     

Twins' reactions to delayed auditory feedback

10 pairs of identical and 10 pairs of fraternal twins, matched by age, spoke under conditions of 0.0-, 100-, 200-, 300-, 400-, and 500-msec. delayed auditory feedback. Length of spoken passages was controlled. Product-moment and intraclass correlations were calculated for speaking times and disfluencies. Significant Pearson rs for times were noted at 0.0 and 300 msec. for both groups and at 100, 200, and 400 msec. for identical twins, while fraternal twins' times were significantly correlated at 500 msec. Difference scores were significantly correlated at 100, 200, 300, and 400 msec. for identical twins. Disfluencies were significantly correlated for identical twins at 400 msec. Data were combined with those of Timmons' (1969) study, increasing subjects to 21 pairs per group. Intraclass correlations supported the contention that responses of identical twin pairs to delayed auditory feedback were more highly correlated than those for fraternal twin pairs.     

Environmental contributions to preschoolers' semantic fluency

Semantic fluency was examined in Hebrew‐speaking 5‐year‐old monozygotic and dizygotic twins (N = 396, 198 pairs), 22% of them with mother‐reported speech‐related problems. There were positive correlations of similar magnitudes among monozygotic, same‐sex dizygotic, and opposite‐sex dizygotic twins. Analyses showed no genetic effects, alongside significant shared (39%) and non‐shared environmental (61%) effects on fluency scores. The presence of speech‐related problems in one twin affected the fluency score of the co‐twin. A multivariate regression analysis revealed that parental education and length of stay at daycare significantly predicted fluency scores. We suggest that semantic fluency performance is highly affected by environmental factors at age 5 although genetic effects might emerge later on.     

Children''s Behavioral Inhibition Over Age and Across Situations: Genetic Similarity for α Trait During Change

Ratings of behaviors pertaining to inhibition were observed for 130 twins participating in a longitudinal study. Ratings were available for four ages (12, 18, 24, and 30 months) and from three sources at each age: direct observations obtained in a laboratory setting, direct observations obtained in conjunction with infant mental testing, and a temperament measure from a questionnaire completed by parents. For the individual twins, the age-to-age correlations were in the moderate range (.26 to .64). The situation-to-situation correlations were generally in the same range (.17 to .64). When the twins were recombined into twin pairs, within-pair (intraclass) correlations indicated that monozygotic (MZ) twins were more concordant than dizygotic (DZ) twins for each of the behaviors at each of the ages. Also, the MZ twins were more concordant for the direction and degree of behavioral change from age to age or from situation to situation. These data provide additional evidence for the biological influence on behavioral inhibition, a characteristic that has been studied in temperament and personality research. The results suggest that the trait of behavioral inhibition and a change in the trait are genetically conditioned. In addition, it is suggested that the concept of trait be expanded to include the person-centered biological regulation of change.     

Growing up and growing apart: a developmental meta-analysis of twin studies

Developmental change in twin similarity was examined with age contrasts in a meta-analysis of twin studies from 1967 through 1985. Intraclass rs were coded from 103 papers that included data for monozygotic or dizygotic twins, or for both, on personality or intelligence variables. Analyses indicated that there was a general tendency for some intraclass rs to decrease with age. In other words, as twins grow up, they grow apart. There were also developmental differences associated with components of variance for heritability, the shared environment, and the nonshared environment. Mechanisms through which the nonshared environment may operate are discussed.     

Personality stability in late adulthood: a behavioral genetic analysis

A sample of 833 twins from the Minnesota Twin Study of Adult Development and Aging completed the Multidimensional Personality Questionnaire (MPQ; Tellegen, 1982) twice, averaging 59.4 (sd=9.7) years of age at first and 64.4 (sd=10.2) years of age at second testing (average retest interval 5.0 years, sd=2.36, range 1.0-10.4 years). Both means and standard deviations of scale scores were extremely stable from first to second testing. In addition, sample participants tended to retain their rank order on the scales (average r=.76 across scales). Bivariate biometric analyses showed that the genetic influences on most of the scale scores were almost perfectly correlated across the two waves (range .95 to 1.00). The nonshared environmental influences were also highly correlated across the two waves (range .53 to .73). Models specifying identical variance components at the two time points and fixing the genetic correlation to 1.00 provided improved fit. The results suggest that the high stability of personality in later adulthood has a strong genetic foundation, supplemented by stability of environmental effects.     

Twin imitation for antisocial behavior: implications for genetic and family environment research.

When twin pairs influence each other's behavior, observed variance is greater for MZ twins than for DZ twins under at least 1 of 2 conditions: (a) the trait has some heritability and (b) MZ twins influence each other more than do DZ twins. Applied to a trait that has an underlying continuous distribution but is measured as a dichotomy, the presence of reciprocal twin influence predicts that if the base rate for the trait is not exactly 50%, then the prevalence of the trait should differ in MZ and DZ twin pairs. This prediction held for registered criminality in a large twin cohort. Methods of analysis that permit reciprocal twin interaction not only provide better statistical fits to the data but also yield estimates of heritability that agree with adoption data. The results suggest that the genetic influence on registered criminality may be more modest than previously thought.     

Huntington disease: A case study describing the complexities and nuances of predictive testing of monozygotic twins

When a candidate for predictive testing for the Huntington disease gene is a monozygotic twin, confidentiality of the co-twin's diagnosis and autonomy of participation are among the critical genetic counseling issues. Predictive testing can proceed when twins voluntarily and simultaneously request counseling and evaluation in an HD testing program. This case describes a young man referred for predictive testing to an HD testing site on the East Coast of the United States. Family history revealed a twin brother of unknown zygosity who resided on the West Coast of the United States. The genetic counselors on opposite coasts collaborated to provide genetic counseling and evaluation for voluntary, informed predictive testing of the twins, protecting their rights while observing national protocol guidelines.     

ABILITIES OF TWINS

The investigation concerns two main problems: (1) the distribution of ability test scores among twins in comparison with single-borns; and (2) intra-pair similarity among the various twin categories. More than 1000 individual twins were compared with 2700 single-borns on 21 test variables covering Swedish, Mathematics and English. The twin group consistently showed a lower average than the single-borns due to a displacement of the test score distribution as a whole among twins. The intra-pair similarities, expressed as intra-class correlations, run between 0.85 and 0.90 for identical pairs, whereas like-sex fraternals showed coefficients about 0.60. The unlike-sex fraternals had coefficients ten to twenty hundredths lower than those of the like-sex pairs.     

Modeling Rater Disagreement for ADHD: Are Parents or Teachers Biased?

The present study is the first to utilize twin modeling to examine whether parent-teacher disagreement for ADHD ratings is due to parent or teacher bias, or due to raters observing different but valid ADHD behaviors. A joint analysis was conducted with 106 twin pairs, including twins selected for ADHD and control twin pairs. Total ADHD scores were analyzed using multiple rater models that estimate genetic and environmental contributions common to both raters and unique to each rater. Results suggest that 1) disagreement in ADHD ratings is strongly due to parents and teachers observing different ADHD behaviors, some of which is valid and some of which is due to bias, and 2) parents may be more biased than teachers in their ADHD ratings.     

Genetic influences on the overlap between low IQ and antisocial behavior in young children

The well-documented relation between the phenotypes of low IQ and childhood antisocial behavior could be explained by either common genetic influences or environmental influences. These competing explanations were examined through use of the Environmental Risk Longitudinal Twin Study 1994-1995 cohort (Moffitt & the E-Risk Study Team, 2002) of 1,116 twin pairs and their families. Children's IQ was assessed via individual testing at age 5 years. Mothers and teachers reported on children's antisocial behavior at ages 5 and 7 years. Low IQ was related to antisocial behavior at age 5 years and predicted relatively higher antisocial behavior scores at age 7 years when antisocial behavior at age 5 years was controlled. This association was significantly stronger among boys than among girls. Genetic influences common to both phenotypes explained 100% of the low IQ-antisocial behavior relation in boys. Findings suggest that specific candidate genes and neurobiological processes should be tested in relation to both phenotypes.     

The effects of shared environment on adult intelligence: A critical review of adoption, twin, and MZA studies

There has been a vigorous debate for decades concerning the heritability of intelligence. In recent years, the debate has been focused on whether the components of IQ variability change with age and on separating environmental effects into shared and unshared components. Citing evidence from adoption studies, studies comparing identical and fraternal twins, and studies of identical twins raised apart, some prominent psychologists have concluded that the shared environment has a significant effect on the intelligence of children but little or no effect on the intelligence of adults. In this article, the evidence from such studies is reviewed. The article reaches the conclusion that while there is some evidence from adoption studies supporting the claim that shared environment has little or no effect on adult intelligence, that evidence is inconclusive and is inconsistent with evidence from twin studies and from studies of identical twins reared apart. (PsycINFO Database Record (c) 2012 APA, all rights reserved).     

Genetic influence on life events during the last half of the life span

Genetic influence on perceptions of major events later in life was assessed with a combination of twin and adoption designs as part of the Swedish Adoption/Twin Study of Aging (SATSA). The SATSA design includes 4 groups totaling 399 pairs of same-sex twins: identical and fraternal twins reared apart and matched twins reared together. The average age of the twins was 59 years. The results demonstrate significant genetic influence on reports of the occurrence of life events, especially for controllable events in which the individual can play an active role. Maximum likelihood model-fitting estimates of genetic influence indicate that 40% of the variance of the total life events score is due to genetic differences among individuals. How genetic factors can affect life experiences and directions for future research are discussed.     

The ethics of separating conjoined twins: two arguments against

I argue that the separation of conjoined twins in infancy or early childhood is unethical (rare exceptions aside). Cases may be divided into three types: both twins suffer from lethal abnormalities, only one twin has a lethal abnormality, or neither twin does. In the first kind of case, there is no reason to separate, since both twins will die regardless of treatment. In the third kind of case, I argue that separation at an early age is unethical because the twins are likely to achieve an irreplaceably good quality of life—the goods of conjoinment—that separation takes away. Evaluation of this possibility requires maturation past early childhood. Regarding the second type, I point out that with conceivable but unrecorded exceptions, these cases will consistently involve sacrifice separation. I present an argument that sacrifice separation is unethical, but in some cases a moral dilemma may exist in which separation and refraining from separation are both unethical. Perhaps in such cases a decision can be made on non-moral grounds; however, the possibility of such a decision serves not to mitigate but to underscore the fact that the separation is unethical. My conclusion, which applies to all three types of cases, is that it is unethical to separate conjoined twins before their developing personalities give some reliable indication as to whether they desire separation and whether they will achieve those goods of conjoinment.     

Twin-singleton differences in verbal ability: Where do they stem from?

In a follow-up investigation at age 9, the cognitive and social characteristics of 35 pairs of twins, studied previously at age 2, were compared with those of matched singletons at school. At age 2, twins' lower verbal ability compared with singletons' was attributed to lesser amount of speech by parents—seen as an outcome of the “twoness” of the “twin situation”—rather than to biological handicap or mother's education. At age 9, twins were equal to singletons in physical development and nonverbal ability, but the monozygotic (MZ)—not the dizygotic (DZ)—twins showed lower verbal ability. However, far more variance in verbal ability was accounted for by mother's education and birthweight than by twinship. In the long run, therefore, mothers' educational differences are more influential than the “twoness” of the “twin situation.”     

“Principles in his nature which interest him in the fortune of others…”: The heritability of empathic concern for others1

The present research was conducted to explore genetic influences on empathic concern for others. First, an index of empathic concern was created by combining relevant items from Gough's Adjective Check List (ACL). This index was validated by correlating scores of 88 undergraduates on the index with their scores on a self-report measure of empathy, which has been related to prosocial behavior. Correlations were sufficiently high to accept the validity of the index. Next, previously collected ACL responses of 114 monozygotic (MZ) and 116 dizygotic (DZ) twins were reanalyzed in order to create an empathic concern score for each twin. The twins were middle-aged males initially raised together but living apart at the time they completed the ACL. Comparison of intraclass correlations for MZ and DZ twins revealed, as predicted by the genetic hypothesis, significant (p < .005) heritability in empathic concern scores. This finding suggests that there may, indeed, be a genetic influence on individual differences in empathic concern for others. Some limitations of the present data are also considered. How selfish soever man may be supposed, there are evidently some principles in his nature which interest him in the fortune of others, and render their happiness necessary to him.     

In search of shared and nonshared environmental factors in security of attachment: a behavior-genetic study of the association between sensitivity and attachment security

The current article presents results from a twin study of genetic and environmental components of maternal sensitivity and infant attachment and their association. The sample consisted of 136 twin pairs from 2 sites: Leiden, the Netherlands, and London, UK. Maternal sensitivity was assessed in the home at 9-10 months, and infant attachment security was observed in the laboratory at 12 months. The study yielded little evidence that genetic factors are involved in variations between twins in maternal sensitivity ratings but did find that shared variance in maternal sensitivity was able to account for some of the similarity between twins in attachment security. Weak nonshared associations between sensitivity and attachment appeared to suppress the magnitude of the correlation between attachment and sensitivity in twin children. The results could indicate that the attachment security of one twin may depend on the relationship the parent has with the other twin. The results are brought to bear on the validity of attachment theory as a theory of primarily shared environmental effects in children's development and the continuing challenge posed to attachment theory by within-family differences in socioemotional processes.     

Behaviour therapy with identical twins

Among the patients treated by the writer during the past five years were two pairs of identical twins. Each respective pair of twins suffered from similar neurotic disabilities. While the patients undergoing behaviour therapy either recovered completely or improved substantially, their untreated twin siblings retained their maladaptive habits until they too underwent a course of behaviour therapy. A fifth patient, also one of an identical twin, derived benefit from therapy while his twin brother, opposed to therapeutic intervention on religious grounds, has remained neurotically incapacitated. These eases are followed by comments drawing didactic inferences. Emphasis is placed on the fact that behaviour therapy does not ignore the complex causality of neurotic disturbances. Interpersonal considerations at both causal and remedial levels are discussed.