Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “heritability”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 73 records · Page 4Linked to original sources

The heritability of hypothalamus pituitary adrenal axis responses to psychosocial stress is context dependent.

Individual differences in the response of the hypothalamus pituitary adrenal axis to stress are known to play an important role in health and disease risk. The origins, or determinants, of these individual differences are not well understood. To date, no study has examined the effects of context on the heritability of psychoendocrine stress responses. In the present study, 58 male twin pairs were exposed to a psychosocial stressor (Trier Social Stress Test) three times at weekly intervals, and their salivary and total cortisol, ACTH, and heart rate responses were assessed. Modest heritabilities were observed for all measures at the first stress exposure (all h2 < 0.33), but heritability estimates increased substantially with repetition of the stressor (T3: all h2 > 0.97). Concurrently, only the first but not the second and third Trier Social Stress Test exposure induced a significant increase in state anxiety (T1: P < 0.01, T2 and T3: n.s.), suggesting low heritabilities in a new, anxiety-evoking context and high heritabilities in a familiar, low-anxiety context. These findings challenge previous reports on a low heritability of markers of stimulated hypothalamus pituitary adrenal axis activity and are the first to document the relevance of context for psychoendocrine heritability estimates.

Adolescent↗

Heritability of changes in bone size and bone mass with age in premenopausal white sisters.

UNLABELLED: Femoral neck area expands and BMD decreases in premenopausal women. We used longitudinal DXA measurements on 388 premenopausal white sisters to show significant heritability of the rates of change in femoral neck area, BMC, and BMD. INTRODUCTION: Bone mass and structure are highly heritable. However, genetic effects on age-related changes in bone mass and structure in adults have been much less studied. MATERIALS AND METHODS: DXA measurements were made on 388 healthy white premenopausal sisters from 178 families. Rates of change in femoral neck area, BMC, and BMD, as well as body weight, were calculated from two measurements made an average of 5.7 years apart. Mixed models were used to test whether bone changes were related to age or weight change. Variance components models were used to estimate the heritability of the rates of change. A method was proposed to correct for the underestimation of heritabilities caused by measurement errors of the rates of change. RESULTS: Femoral neck area increased with age, whereas BMD decreased. All of the rates of change at the femoral neck were positively correlated with weight change, but the rates of femoral neck changes did not vary with age. Adjusted for weight change, change in femoral neck BMC became negative. Significant heritabilities (0.29-0.36) were detected for changes in femoral neck BMC, BMD, and area adjusted for weight changes. Correction for DXA measurement error in the rate estimates increased the heritability estimates (from 0.29-0.36 range to 0.37-0.64 range). CONCLUSIONS: Rates of change are heritable for femoral neck area, BMC, and BMD in premenopausal white women.

Adult↗

Heritabilities of apolipoprotein and lipid levels in three countries.

This study investigated the influence of genes and environment on the variation of apolipoprotein and lipid levels, which are important intermediate phenotypes in the pathways toward cardiovascular disease. Heritability estimates are presented, including those for apolipoprotein E and AII levels which have rarely been reported before. We studied twin samples from the Netherlands (two cohorts; n = 160 pairs, aged 13-22 and n = 204 pairs, aged 34-62), Australia (n = 1362 pairs, aged 28-92) and Sweden (n = 302 pairs, aged 42-88). The variation of apolipoprotein and lipid levels depended largely on the influences of additive genetic factors in each twin sample. There was no significant evidence for the influence of common environment. No sex differences in heritability estimates for any phenotype in any of the samples were observed. Heritabilities ranged from 0.48-0.87, with most heritabilities exceeding 0.60. The heritability estimates in the Dutch samples were significantly higher than in the Australian sample. The heritabilities for the Swedish were intermediate to the Dutch and the Australian samples and not significantly different from the heritabilities in these other two samples. Although sample specific effects are present, we have shown that genes play a major role in determining the variance of apolipoprotein and lipid levels in four independent twin samples from three different countries.

Adolescent↗

Within-herd heritability estimated with daughter-parent regression for yield and somatic cell score.

Estimates of heritability within herd (h(WH)(2) ) that were generated with daughter-dam regression, daughter-sire regression, and REML were compared, and effects of adjusting lactation records for within-herd heritability on genetic evaluations were evaluated. Holstein records for milk, fat, and protein yields and somatic cell score (SCS) from the USDA national database represented herds in the US Northeast, Southeast, Midwest, and West. Four data subsets (457 to 499 herds) were randomly selected, and a large-herd subset included the 15 largest herds from the West and 10 largest herds from other regions. Subset heritabilities for yield and SCS were estimated assuming a regression model that included fixed covariates for effects of dam yield or SCS, sire predicted transmitting ability (PTA) for yield or SCS, herd-year-season of calving, and age within parity. Dam records and sire PTA were nested within herd as random covariates to generate within-herd heritability estimates that were regressed toward mean h(WH)(2) for the random subset. Heritabilities were estimated with REML using sire models (REML(SIRE)), sire-maternal grandsire models (REML(MGS)), and animal models (REML(ANIM)) for each herd individually in the large-herd subset. Phenotypic variance for each herd was estimated from herd residual variance after adjusting for effects of year-season and age within parity. Deviations from herd-year-season mean were standardized to constant genetic variance across herds, and records were weighted according to estimated error variance to accommodate h(WH)(2) when estimating breeding values. Mean h(WH)(2) tended to be higher with daughter-dam regression (0.35 for milk yield) than with daughter-sire regression (0.24 for milk yield). Heritability estimates varied widely across herds (0.04 to 0.67 for milk yield estimated with daughter-dam regression), and h(WH)(2) deviated from subset means more for large herds than for small herds. Correlation with REML(ANIM) h(WH)(2) was 0.68 for daughter-dam and was 0.45 for daughter-sire h(WH)(2) for milk yield. The correlation between daughter-sire h(WH)(2) and REML(MGS) was greater than the correlation between daughter-dam h(WH)(2) and REML(MGS). Data adjustments had a minimal impact on breeding value bias. Within-herd heritability can be estimated rapidly using regression techniques with moderate accuracy, but adjusting lactation records for h(WH)(2) resulted in only a small improvement in the accuracy of genetic evaluations.

Animals↗

The heritability of attitudes: a study of twins.

The genetic basis of individual differences in attitudes was examined in a survey of 195 pairs of monozygotic twins and 141 pairs of same-sex dizygotic twins. A principal components analysis of the 30 attitude items in the survey identified 9 attitude factors, of which 6 yielded significant heritability coefficients. Nonshared environmental factors accounted for the most variance in the attitude factors. Possible mediators of attitude heritability were also assessed, including personality traits, physical characteristics, and academic achievement. Analyses showed that several of these possible mediators correlated at a genetic level with the heritable attitude factors, suggesting that the heritability of the mediator variables might account for part of the heritable components of some attitudes. There was also some evidence that highly heritable attitudes were psychologically "stronger" than less heritable attitudes.

Achievement↗

The behaviors of some heritability estimators in the complete absence of genetic factors.

Heritability is an important concept in quantitative genetics and is widely used in human genetics. A high or even a moderate value of heritability estimate is usually taken as evidence for a genetic component for a quantitative trait. In this paper, the behaviors of some correlation-based heritability estimators are reexamined under the assumption of complete absence of any genetic factors. It turns out that when monozygotic (MZ) twins (or full sibs) are environmentally more similar than dizygotic twins (or half sibs), or when there is placement bias in MZ twins reared apart, those correlation-based heritability estimates can lead to nonnegligible or even high heritability values, even when genetic factors are completely absent. These alarming results suggest that extreme care should be exercised when using these heritability estimators.

Data Interpretation, Statistical↗

Heritability of subclinical atherosclerosis in Latino families ascertained through a hypertensive parent.

Although clinical coronary heart disease and many cardiovascular risk factors are well known to aggregate within families, the heritability of carotid artery intima-media thickness (IMT) is less well documented. We report IMT heritability estimates in Mexican American, Salvadoran American, or Guatemalan American (all referred to as Latino) families ascertained through a hypertensive proband. IMT and cardiovascular risk factors (age, sex, blood pressure, body mass index, lipids, fasting glucose, and insulin sensitivity) were measured in 204 adult offspring of 69 hypertensive probands, along with 82 parents (54 probands and 28 spouses). In the offspring, variance component analysis revealed a heritability for IMT of 64% (P< 0.0001) after adjustment for significant cardiovascular risk factors. Genetic factors accounted for 50% of the total variation in IMT, whereas significant cardiovascular risk factors explained 22% (14% were due to age). For offspring and parents combined, adjusted IMT heritability was less, 34% (P=0.0005), with genetic factors accounting for 18% of the total IMT variation, whereas significant cardiovascular risk factors explained 46% (38% were due to age). We conclude that variation in common carotid artery IMT is heritable in Latino families with a hypertensive proband. Heritability is particularly evident in younger family members, suggesting that acquired factors contribute progressively to IMT variability with aging.

Adolescent↗

Age-stratified heritability estimation in the Framingham Heart Study families.

The Framingham Heart Study provides a unique source of longitudinal family data related to CVD risk factors. Age-stratified heritability estimates were obtained over three age groups (31-49 years, 50-60 years, and 61-79 years), reflecting the longitudinal nature of the data, for four quantitative traits. Age-adjusted heritability estimates were obtained at a single common time point for the same four quantitative traits. The importance of these groups is that they consist of the same individuals. The highest age-stratified heritability estimate (h2 = 0.88 (+/- 0.06)) was for height in the model adjusting for gender over all three age groups. SBP gave the lowest heritability estimate (h2 = 0.15 (+/- 0.11)) for the 70 age group in the model adjusting for gender, height, BMI, smoker, and drinker. BMI had slightly higher estimates (h2 = 0.64 (+/- 0.11)) in the 40 age group than previously published. The highest age-adjusted heritability estimate (h2 = 0.90 (+/- 0.06)) was for height in the model adjusting for gender. SBP gave the lowest heritability estimate (h2 = 0.38 (+/- 0.09)) for unadjusted model. These results indicate that some common, complex traits may vary little in their genetic architecture over time and suggest that a common set of genes may be contributing to observed variation for these longitudinally collected phenotypes.

Adult↗

Heritability and tissue specificity of expression quantitative trait loci.

Variation in gene expression is heritable and has been mapped to the genome in humans and model organisms as expression quantitative trait loci (eQTLs). We applied integrated genome-wide expression profiling and linkage analysis to the regulation of gene expression in fat, kidney, adrenal, and heart tissues using the BXH/HXB panel of rat recombinant inbred strains. Here, we report the influence of heritability and allelic effect of the quantitative trait locus on detection of cis- and trans-acting eQTLs and discuss how these factors operate in a tissue-specific context. We identified several hundred major eQTLs in each tissue and found that cis-acting eQTLs are highly heritable and easier to detect than trans-eQTLs. The proportion of heritable expression traits was similar in all tissues; however, heritability alone was not a reliable predictor of whether an eQTL will be detected. We empirically show how the use of heritability as a filter reduces the ability to discover trans-eQTLs, particularly for eQTLs with small effects. Only 3% of cis- and trans-eQTLs exhibited large allelic effects, explaining more than 40% of the phenotypic variance, suggestive of a highly polygenic control of gene expression. Power calculations indicated that, across tissues, minor differences in genetic effects are expected to have a significant impact on detection of trans-eQTLs. Trans-eQTLs generally show smaller effects than cis-eQTLs and have a higher false discovery rate, particularly in more heterogeneous tissues, suggesting that small biological variability, likely relating to tissue composition, may influence detection of trans-eQTLs in this system. We delineate the effects of genetic architecture on variation in gene expression and show the sensitivity of this experimental design to tissue sampling variability in large-scale eQTL studies.

Alleles↗

The effect of simulated censored data on estimates of heritability of longevity in the Thoroughbred racing industry.

We examined the impact of censored data on estimates of heritability of longevity. Longevity, defined as the length of productive racing life of an individual, is influenced by many factors. A simulated data set, modelled on the Irish Thoroughbred industry, was used to estimate heritabilities of longevity. Several scenarios representing various levels of censoring of performance data were created. The heritability of longevity was estimated for each scenario and compared to the estimated heritability of 0.120 for the complete data set. It was found that the estimates of heritability (0.107, 0.106, 0.082) were biased downwards with (10, 20, and 25%, respectively) censoring of data from poor-performing animals. We found that for a complete reporting it is necessary to reduce bias in the estimation of heritability of longevity.

Algorithms↗

Heritable cell cycle disturbances and late recovery in x-irradiated murine lymphoma L5178Y-S cell populations in vitro.

1. Ionizing radiation can induce in mammalian cells, besides the lethal effects, also heritable damages which retard cell cycle traverse for considerable humber of cell generationsl 2. Radiation-induced heritable lesions in murine leukaemic lymphoblasts L5178Y-S affect progesssion of the cells through the G2 phase of the cell cycle. 3. Late recovery of proliferative activity which must be connected with elimination of the G2 block is a common phenomenon in the heritably damaged L5178Y-S sublines derived from single cells. 4. A possibility should be taken into consideration of employing the cells heritably damaged by radiation as convenient models for studies on some disturbances which accompany ageing of the mammalian cells. 5. It seems that results of studies on both the cells heritably damaged by radiation and the ageing cells could be useful for evaluation of possibilities of prevention, control or elimination of the heritable cell cycle disturbances.

Animals↗

Heritability of cognitive abilities in adult twins: comparison of Minnesota and Swedish data.

Cross-sectional reports suggest heritability of cognitive ability increases throughout adulthood. To investigate this hypothesis, quantitative genetic analyses were conducted on four measures of cognitive ability (verbal, spatial, perceptual speed, memory). Data from Minnesota and Swedish twin studies of aging were compared. Heritability estimates and the factor structure of cognitive abilities could be equated across younger twins (age, 27-50) and middle-aged twins (age, 50-65) from both studies, suggesting stability of heritability during adulthood. The heritability of 81% for a general cognitive factor confirmed earlier findings of high heritability in younger and middle-aged samples. Older Swedish twins (age, 65-85) demonstrated significantly lower heritability estimates for cognitive abilities (54%) and a significantly different factor structure of cognitive ability.

Adult↗

Sex differences in heritability of sensitization to Blomia tropicalis in asthma using regression of offspring on midparent (ROMP) methods.

A genetic basis for asthma- and atopy-related quantitative traits, such as allergen-specific immunoglobulin E (IgE) levels, has been suggested by the observed familial aggregation of these traits in temperate climates. Less information is available for tropical climates, where different allergens may predominate. Sensitivity to the mite Blomia tropicalis is related to asthma in tropical climates, but heritability of B. tropicalis sensitivity and the impact of age, sex, and other environmental covariates on heritability have not been widely explored. Total and specific IgE levels were measured by immunochemiluminescent assay in 481 members of 29 Barbadian families (comprised of 340 parent-offspring trios or pairs) ascertained through two asthmatic siblings. Trait heritability was estimated using regression of offspring on mid-parent (ROMP) and pairwise correlation analysis of unadjusted IgE levels and on residual values after adjustment for covariates. Heritability of IgE levels to the major antigen of B. tropicalis (Blo t M) estimated by ROMP in 180 complete parent-offspring trios was 0.56. Heritability was consistently greater for male offspring than for female offspring. Similar sex-specific patterns were observed for specific IgE to Dermatophagoides pteronyssinus and total IgE levels and were relatively unaffected by adjustment for covariates. Pairwise correlational analyses of specific and total IgE levels showed similar results. Moderate heritability of Blo t M IgE levels was detected in these Barbadian families and was greater for sons than daughters. Adjustment for covariates had minimal impact. This suggests that future investigations of genetic determinants of IgE levels should include approaches that allow for potential sex differences in their expression.

Acari↗

Heritability and reliability of P300, P50 and duration mismatch negativity.

BACKGROUND: Event-related potentials (ERPs) have been suggested as possible endophenotypes of schizophrenia. We investigated the test-retest reliabilities and heritabilities of three ERP components in healthy monozygotic and dizygotic twin pairs. METHODS: ERP components (P300, P50 and MMN) were recorded using a 19-channel electroencephalogram (EEG) in 40 healthy monozygotic twin pairs, 19 of them on two separate occasions, and 30 dizygotic twin pairs. Zygosity was determined using DNA genotyping. RESULTS: High reliabilities were found for the P300 amplitude and its latency, MMN amplitude, and P50 suppression ratio components. ICC=0.86 and 0.88 for the P300 amplitude and P300 latency respectively. Reliability of MMN peak amplitude and mean amplitude were 0.67 and 0.66 respectively. P50 T/C ratio reliability was 0.66. Model fitting analyses indicated a substantial heritability or familial component of variance for these ERP measures. Heritability estimates were 63 and 68% for MMN peak amplitude and mean amplitude respectively. For P50 T/C ratio, 68% heritability was estimated. P300 amplitude heritability was estimated at 69%, and while a significant familiality effect was found for P300 latency there was insufficient power to distinguish between shared environment and genetic factors. CONCLUSIONS: The high reliability and heritability of the P300 amplitude, MMN amplitude, and P50 suppression ratio components supports their use as candidate endophenotypes for psychiatric research.

Adult↗

The NHLBI Twin Study: heritability of apolipoprotein A-I, B, and low density lipoprotein subclasses and concordance for lipoprotein(a).

Heritability of plasma apolipoprotein (apo) A-I, apo B, and low density lipoprotein (LDL) subclasses and concordance for lipoprotein(a) excess were assessed in 109 monozygotic (MZ) and 113 dizygotic (DZ) twin pairs participating in the third examination of the National Heart, Lung, and Blood Institute Twin Study. The intraclass correlation coefficient for apo A-I was significantly greater in MZ twins (0.56) than in DZ twins (0.37, P less than 0.05); however, apo A-I showed an unequal distribution in the two groups, with significantly greater total variance in DZ twins. Therefore the among-component estimate of genetic variance was applied, and the results indicated no significant heritability for apo A-I (P = 0.59). MZ and DZ twins had equal apo B variance. The intraclass correlation coefficient for apo B in MZ twins (0.71) was significantly higher than in DZ twins (0.25) (P less than 0.0001), indicating significant heritability for apo B. Plasma apo A-I levels were significantly correlated with alcohol intake (P less than 0.0001), body mass index (BMI, P less than 0.0001), and physical activity, while apo B levels were significantly correlated only with BMI (P less than 0.05). After plasma apo A-I and apo B concentrations were adjusted for all of these variables and for cigarette smoking, the analysis of variance and intraclass correlation coefficients remained virtually unchanged. The LDL type intraclass correlation coefficient was higher in MZ twins (0.58) than in DZ twins (0.32, P less than 0.005); however, greater total variance for this parameter in DZ twins was observed and after applying the among component estimate of genetic variance, no significant heritability of LDL type was observed. After adjustment for covariate effects the conclusions were not changed. Only 8.4% of MZ twin pairs, as compared with 26.7% of DZ twin pairs, were discordant for elevated lipoprotein(a) on gradient gels (P less than 0.0001). Our data indicate that there is a strong heritability for plasma apo B and lipoprotein(a), with only weak evidence for heritability of LDL type or plasma apo A-I levels within this population sample.

Aged↗

Heritable translocation test in mice.

The status of the heritable-translocation test in mice with respect to its usefulness in practical testing was evaluated by using information available in the open literature. A total of 47 reports were evaluated; 29 were judged to contain adequate information to classify whether or not a given chemical induced heritable translocations. Heritable-translocation data were available for 32 compounds; data were not adequate for 15 compounds. Of the remaining 17 compounds, clear-cut determination of positive or negative effects was made for 14 compounds, while data for 3 compounds were only suggestive of either negative or positive effects. 10 chemicals have been shown to induce heritable translocations. These chemicals are either direct or indirect alkylating agents. The heritable-translocation test needs to be improved before it can be used in wide-scale practical testing. The most important question is whether or not historical controls can be used in tests for significance; the cost of concurrent controls is prohibitive. There is a need to standardize methods used in testing laboratories with respect to the size of error involved in classifying translocation heterozygotes and the power of the test. There is also a need to study in the effectiveness of non-alkylating clastogens in inducing heritable translocations in mice.

Animals↗

Heritability of craniofacial characteristics between parents and offspring estimated from lateral cephalograms.

OBJECTIVE: The purpose of the study was to estimate the heritability of different cephalometric parameters, according to lateral cephalograms, between parents and their offspring in an Icelandic population. METHODS: The material was collected at the Faculty of Odontology, University of Iceland. The subjects were 363 children (6 years of age) and their parents. Material was also collected from the same group of children at the age of 16 years. Twenty-two reference points were identified on each cephalogram, and 33 variables were calculated, both angular and linear. Heritability was calculated at ages 6 and 16. RESULTS: Daughters had more variables that reached the level of significance than did sons. Daughters showed similar heritability to both parents at both age levels, but more variables were highly significant ( P < or = .001) in the daughter-father groups. Sons showed stronger heritability to their mothers at both ages. The variables showing the greatest heritability were those representing the position of the lower jaw, the anterior and posterior face heights, and the cranial base dimensions. Heritability was notably low for the dental variables. CONCLUSIONS: Genetic aberrations can be detected for complex polygenetic multifactorial traits. Cephalometric data can support predictions, and analysis of parental data could have predictive value for offspring.

Adolescent↗

Heritability of menopausal age in mothers and daughters.

OBJECTIVE: To determine the heritability of age at natural menopause from mother-daughter pairs. DESIGN: Two-generation families were selected to study heritability of menopausal age. SETTING: Subjects were drawn from a population-based study. PATIENT(S): One hundred sixty-four mother-daughter pairs with a natural menopausal age. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): The heritability of age at natural menopause estimated by a random-effects model. RESULT(S): A heritability of 44% (95% confidence interval, 36%, 50%) was estimated. CONCLUSION(S): This study confirms that heritable components largely determine the natural age at menopause. Reasons for the differences between heritability estimates based on sibling pairs and parent-child comparisons are discussed.

Aging↗