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Genetic selection for health traits using producer-recorded data. II. Genetic correlations, disease probabilities, and relationships with existing traits.

The objectives of this study were to calculate genetic correlations between health traits that were recorded in on-farm herd management software programs and to assess relationships between these traits and other traits that are routinely evaluated in US dairy sires. Data consisted of 272,576 lactation incidence records for displaced abomasum (DA), ketosis (KET), mastitis (MAST), lameness (LAME), cystic ovaries (CYST), and metritis (MET) from 161,622 cows in 646 herds. These data were collected between January 1, 2001 and December 31, 2003 in herds using the Dairy Comp 305, DHI-Plus, or PCDART herd management software programs. Binary incidence data for all disorders were analyzed simultaneously using a multiple-trait threshold sire model that included random sire and herd-year-season of calving effects. Although data from multiple lactations were available for some animals, our genetic analysis included only first parity records due to concerns about selection bias and improper modeling of the covariance structure. Heritability estimates for the presence or absence of each disorder during first lactation were 0.14 for DA, 0.06 for KET, 0.09 for MAST, 0.03 for LAME, 0.04 for CYST, and 0.06 for MET. Estimated genetic correlations were 0.45 between DA and KET, 0.42 between KET and CYST, 0.20 between MAST and LAME, 0.19 between KET and LAME, 0.17 between DA and CYST, 0.17 between KET and LAME, 0.17 between KET and MET, and 0.16 between LAME and CYST. All other correlations were negligible. Correlations between predicted transmitting abilities for the aforementioned health traits and existing production, type, and fitness traits were low, though it must be noted that these estimates may have been biased by low reliability of the health trait evaluations. Based on results of this study, it appears that genetic selection for health disorders recorded in on-farm software programs can be effective. These traits can be incorporated into selection indices directly, or they can be combined into composite traits, such as "reproductive disorders", "metabolic disorders", or "early lactation disorders".

Abomasum↗

Investigating the causal role of smoking in gout: A triangulation approach combining NHANES data, genetic correlation, and Mendelian randomization.

The relationship between smoking and the development of gout is not well understood. To address this, we adopted a triangulation framework that integrates observational analysis, genetic correlation estimation, and two-sample Mendelian randomization (MR) to examine whether smoking confers a causal risk for gout. We first performed a cross-sectional analysis using information for 13,626 participants from the National Health and Nutrition Examination Survey between 2013 and 2018. The association of smoking with gout was subsequently assessed through logistic regression models. We next investigated the extent of shared genetic factors between smoking phenotypes and gout. We were able to demonstrate this using the linkage disequilibrium score regression applied to genome-wide association study data of European ancestry. Finally, to verify the causality of our relationship, we carried out a two-sample MR analysis. We selected the inverse-variance weighted (IVW) method and confirmed the consistency of using the IVW method with other statistical methods, including weighted median, weighted mode, and simple mode, as well as MR-Egger regression. We performed sensitivity analyses to investigate the heterogeneity of the hypothesis and stability of the data. Our findings based on National Health and Nutrition Examination Survey data reveal that there is a strong positive association between smoking and the risk of gout (odds ratio [OR]&#x2005;=&#x2005;1.94, 95% confidence interval [CI]&#x2005;=&#x2005;1.48-2.55, P&#x2005;<&#x2005;.001). This association persisted after confounding adjustments (OR&#x2005;=&#x2005;1.41, 95% CI&#x2005;=&#x2005;1.04-1.91, P&#x2005;=&#x2005;.027). In the subgroup analyses, former smokers and current smokers of 10 to 20 cigarettes per day had a substantially increased risk. Post-linkage disequilibrium score regression analysis revealed that the significantly positive genetic correlations of smoking initiation and lifetime smoking index with gout risk were both significantly positive. Additional evidence for causality is presented by MR. Genetic prediction of smoking initiation statistically increases gout risk (IVW OR&#x2005;=&#x2005;1.55, 95% CI&#x2005;=&#x2005;1.26-1.90, P&#x2005;=&#x2005;3.17&#x2005;&#xd7;&#x2005;10-5). A much stronger association is evident for lifetime smoking index (IVW OR&#x2005;=&#x2005;1.99, 95% CI&#x2005;=&#x2005;1.44-2.76, P&#x2005;=&#x2005;3.24&#x2005;&#xd7;&#x2005;10-5). These findings are the same with or without heterogeneity by sensitivity analysis. In light of our integrated analysis, smoking is a causative factor for gout. This suggests that public health interventions like anti-smoking campaigns might reduce gout incidence.

Humans↗

Genotype by environment interaction and genetic correlations among parities for somatic cell count and milk yield.

Lactation measures of somatic cell concentration and total SCC production were developed. Data were separated into three parity groups. Within parity, five data sets were created: four subsets by herd-year average SCC, and one with all records. Records on lactation SCC, total SCC production, and 305-d milk were analyzed by a sire model separately in each subset within parity. Variance components estimates were by REML. For SCC and total SCC production, heritability estimates averaged .12 and were lowest in the highest level of herd-year average SCC. Estimates of genetic correlation between SCC and total SCC production were over .95; between SCC and 305-d milk were around .25 in first and -.15 in later parities; between total SCC and 305-d milk were around .50 in first and .15 in later parities. Product-moment correlations between sire effects in different levels of herd-year average SCC were obtained. Ratios of product-moment correlations to their expected value were above .80 for all traits in all parities. High ratios indicated little genotype by environment interaction. A sire by herd interaction was fitted in the model and accounted for less than 2% of total phenotypic variance for SCC and total SCC production, and 4% for 305-d milk. Estimates of genetic correlation of first with later parities were .71 to .86 for all traits. Between second and third parity genetic correlation estimates were around unity for all traits. Records from all parities should be used for sire evaluation.

Animals↗

Subjective well-being is heritable and genetically correlated with dominance in chimpanzees (Pan troglodytes).

The hypothesis that subjective well-being (SWB) is heritable and genetically correlated with Dominance was tested using 128 zoo chimpanzees. Dominance was a chimpanzee-specific personality factor including items reflecting Extraversion and low Neuroticism. SWB was measured with a 4-item scale. The best behavior genetic model included additive genetic and nonshared environmental effects for SWB and Dominance, marginal matemal effects for SWB, a high genetic correlation, and a low nonshared environmental correlation. Results indicated that the shared variance between SWB and Dominance was a consequence of common genes and that the unique variance between SWB and Dominance was a consequence of the nonshared environment. These findings indicate that common genes may underlie the correlation between human personality factors and SWB.

Animals↗

Fat deposition in a broiler sire strain. 3. Heritability of and genetic correlations among body weight, abdominal fat, and feed conversion.

Body weight, abdominal fat, and feed conversion were measured in ad libitum-fed pedigreed chickens of four lines selected from a broiler sire strain. Lines were selected for four generations for a low amount of abdominal fat (AF), a favorable feed conversion (FC), a high body weight after restricted feeding (GR), and a high body weight after ad libitum feeding (GL). A total of 2,400 pedigreed chickens from three hatches were reared by line in groups on litter and 864 chickens were tested for individual feed conversion in individual cages. The h2 from the sire component for the four lines combined were for body weight, .27 (litter) and .22 (cages); for weight of abdominal fat, .54 (litter) and .40 (cages); for percentage abdominal fat, .53 (litter) and .45 (cages); and for feed conversion, .44 (cages). Analysis within line and sex indicated that, in the relatively fat GR and GL lines, sex-linked inheritance could be involved for abdominal fat. In the leaner AF and FC lines this was not the case. Genetic correlations (sire estimate) for the four lines combined were, between body weight and weight of abdominal fat, .58 (litter) and .55 (cages); between body weight and percentage abdominal fat, .36 (litter) and .47 (cages); between body weight and feed conversion, .16 (cages); between weight of abdominal and feed conversion, .43 (cages); and between percentage abdominal fat and feed conversion, .44 (cages). Genetic correlations did not differ significantly between sexes, but in the AF and FC lines, the genetic correlation between body weight and abdominal fat was higher (AF: .80, FC: .76) than in the GR (.14) and GL (.68) lines.

Abdomen↗

Phenotypic and genetic correlation between egg characters and embryo and chick weights of Alexandria and Fayoumi chickens.

At the Poultry Research Centre of Alexandria University phenotypic and genetic correlations were estimated on the basis of dam averages of three populations between egg quality features, embryo and chick weights. The relationships of individual egg weight, shell weight, and shell thickness as well as the egg shape on the one hand and the embryo weight at 6, 12, and 18 days of age on the other hand were weak and exhibited no uniform trend. The correlations between egg weight and chick weight were also low. The genetic correlations between shell weight and shell thickness and the chick weight up to the eighth week were even negative.

Animals↗

Genetic correlation between boars, barrows and gilts for various carcass traits.

Data from 11 generations of a selection study were analyzed to estimate genetic correlations between boars and gilts, boars and barrows, and gilts and barrows for carcass traits in the Lacombe and Yorkshire breeds of swine. Genetic correlations were estimated to determine if genotype X sex interactions existed and to assess the need for separate genetic parameters for boars and gilts in selection response equations. Genotype X sex interactions were found for total carcass fat/kg of cold carcass weight, area of lean in the ham face/kg of cold carcass weight and percent lean in the ham face/kg of cold carcass weight. Carcass length, longissimus muscle area/kg of cold carcass weight percent ham of side and percent lean in the ham face did not have genotype X sex interactions. Selection based on pooled genetic parameters over sex were favored over selection based on separate genetic parameters regardless of the presence or absence of genotype X sex interactions.

Animals↗

Short communication: genetic correlation between test-day electrical conductivity of milk and mastitis.

Electrical conductivity (EC) of milk is an indicator of mastitis. If EC shows genetic variation and is genetically correlated to mastitis, it could be used in a breeding program that includes selection for improved mastitis resistance. In this study, daily records of EC and mastitis from about 1,500 Holstein cows were analyzed. A bivariate animal model was used for estimation of (co)variance components, including fixed effects of age of calving, herd-test-day, and days in milk, in addition to random additive genetic effects and permanent environmental effects. For EC, the estimated heritability was moderate (0.22 to 0.39), whereas for mastitis, the heritability was low (0.013). The genetic correlation between EC and mastitis was estimated to be 0.75, and genetic improvement of mastitis resistance should be feasible through selection for reduced EC.

Analysis of Variance↗

[Relation between paranoid psychoses and schizophrenia (according to genetic-correlation analysis)].

The author has made a genetic-correlational analysis of the findings obtained in a clinical-genealogical examination of two groups of probands--with paranoiac schizophrenia (40 families) and with progressive schizophrenia (365 families). The results of the analysis suggest that the studied forms of schizophrenia are of the same genetic nature. Simultaneously, a genotypical homogeneity of the paranoiac form of schizophrenia has been demonstrated.

Adult↗

Laboratory estimates of heritabilities and genetic correlations in nature.

A lower bound on heritability in a natural environment can be determined from the regression of offspring raised in the laboratory on parents raised in nature. An estimate of additive genetic variance in the laboratory is also required. The estimated lower bounds on heritabilities can sometimes be used to demonstrate a significant genetic correlation between two traits in nature, if their genetic and phenotypic correlations in nature have the same sign, and if sample sizes are large, and heritabilities and phenotypic and genetic correlations are high.

Animals↗

[Genetic effects on grain shape traits of indica black pericarp rice and their genetic correlations with main mineral element contents in grains].

Complete diallel crosses with 7 varieties of indica black pericarp rice were conducted to analyze the genetic effects on grain shape traits such as 100-grain weight, grain length, grain width and length/width and their genetic correlations with main mineral elements of Fe, Zn, Mn and P contents in kernels of parents and their F1s and F2s, by using the full genetic model including seed, cytoplasmic and maternal effects on quantitative traits of seeds in cereal crops. The results indicated that the grain shape traits were controlled by seed direct genetic effects, maternal genetic effects as well as by cytoplasmic effects. The seed direct genetic effects were more important than the maternal genetic effects for grain shape traits, and seed direct additive effects constituted a major part of their genetic effects. The narrow heritabilities of seed direct effects were high for 100-grain weight, grain width and grain length/grain width, while those of seed and maternal effects were intermediate for grain length. Therefore, more attention should be paid to the single seed selection on the 100-grain weight, grain width and grain length/grain width in early generations of hybrid offspring, while in the case of grain length, attention should be paid to single plant selection and single seed selection in late generations. The results also showed that there existed significant genetic correlations of seed direct additive, seed direct dominance, cytoplasm, maternal additive and maternal dominance between most of grain shape traits such as 100-grain weight, grain length, grain width, grain length/grain width and main mineral elements of Fe, Zn, Mn and P contents in grains. The improvement for nutrient quality traits of main mineral elements Fe, Zn, Mn and P contents in indica black pericarp rice could be realized by the indirect selection of grain shape traits in speciality rice quality breeding.

Crosses, Genetic↗

Genetic correlations among sex-limited traits in beef cattle.

Data from a comprehensive germ plasm evaluation program were used to estimate genetic correlations of reproductive and maternal traits of beef females with growth and carcass traits of their steer paternal half-sibs. The data set consisted of 187 sires with approximately four female and five male progeny each. Heritability estimates for age at puberty, weight at puberty, conceptions/service, gestation length, calving difficulty, progeny birth weight, progeny preweaning daily gain and mature weight measured on females were .613 +/- .177, .700 +/- .114, .026 +/- .126, .298 +/- .175, .217 +/- .175, .374 +/- .174, .094 +/- .161, and .540 +/- .150, respectively. Postweaning daily gain, carcass weight, fat trim weight and retail product weight measured on male half-sibs had estimated heritabilities of .363 +/- .090, .441 +/- .093, .502 +/- .093 and .451 +/- .093, respectively. The estimated genetic correlations suggest that selection for postweaning daily gain would result in increased age and weight at puberty, increased mature weight, improved fertility, reduced maternal gestation length, reduced maternal calving difficulty, increased maternal birth weight and reduced maternal preweaning gain. Predicted correlated responses to selection for reduced fat trim at a constant age were increased age and weight at puberty, increased mature weight, reduced maternal fertility, reduced maternal preweaning gain and increased maternal gestation length, birth weight and calving difficulty. Consequences of selection for increased age constant retail product weight or carcass weight appear to be increased age and weight at puberty, increased mature weight, improved fertility, increased maternal gestation length and maternal birth weight but reduced maternal difficulty and reduced maternal preweaning gain.

Animals↗

Genetic analyses of mastitis data using animal threshold models and genetic correlation with production traits.

In the present study, 6 different mastitis data sets of 3 dairy herds with an overall herd size of 3200 German Holstein cows were analyzed. Data collection periods included the first 50, 100, or 300 d of lactation. The 3 data collection periods were analyzed with a lactation model and a test-day model. All models were animal threshold models. Mastitis frequencies in the lactation model data sets varied between 29 and 45%, and varied between 3 and 6% in the test-day model data sets. Depending on the period of data collection, heritabilities of liability to mastitis in the lactation models were 0.05 (50 d), 0.06 (100 d), and 0.07 (300 d). In the test-day models, heritabilities were slightly higher with values of 0.09 (50 and 100 d), and 0.06 (300 d). Between lactation models, the rank correlations between the relative breeding values were high and varied between 0.86 and 0.94. Rank correlations between the relative breeding values of the test-day models ranged from 0.68 to 0.87. The rank correlations between the relative breeding values of lactation models and test-day models varied from 0.51 and 0.80. Genetic correlations between mastitis and milk production traits were estimated with a linear animal test-day model. The correlations with mastitis were 0.29 (milk yield), 0.30 (fat yield), 0.20 (fat content), 0.34 (protein yield), and 0.20 (protein content). The estimated genetic correlation between mastitis and somatic cell score was 0.84.

Animals↗

Genetic correlations among body condition score, yield, and fertility in first-parity cows estimated by random regression models.

Twenty type classifiers scored body condition (BCS) of 91,738 first-parity cows from 601 sires and 5518 maternal grandsires. Fertility data during first lactation were extracted for 177,220 cows, of which 67,278 also had a BCS observation, and first-lactation 305-d milk, fat, and protein yields were added for 180,631 cows. Heritabilities and genetic correlations were estimated using a sire-maternal grandsire model. Heritability of BCS was 0.38. Heritabilities for fertility traits were low (0.01 to 0.07), but genetic standard deviations were substantial, 9 d for days to first service and calving interval, 0.25 for number of services, and 5% for first-service conception. Phenotypic correlations between fertility and yield or BCS were small (-0.15 to 0.20). Genetic correlations between yield and all fertility traits were unfavorable (0.37 to 0.74). Genetic correlations with BCS were between -0.4 and -0.6 for calving interval and days to first service. Random regression analysis (RR) showed that correlations changed with days in milk for BCS. Little agreement was found between variances and correlations from RR, and analysis including a single month (mo 1 to 10) of data for BCS, especially during early and late lactation. However, this was due to excluding data from the conventional analysis, rather than due to the polynomials used. RR and a conventional five-traits model where BCS in mo 1, 4, 7, and 10 was treated as a separate traits (plus yield or fertility) gave similar results. Thus a parsimonious random regression model gave more realistic estimates for the (co)variances than a series of bivariate analysis on subsets of the data for BCS. A higher genetic merit for yield has unfavorable effects on fertility, but the genetic correlation suggests that BCS (at some stages of lactation) might help to alleviate the unfavorable effect of selection for higher yield on fertility.

Animals↗

Genetic correlations between two strains of Durocs and crossbreds from differing production environments for slaughter traits.

The aim of this study was to estimate the genetic correlations between 2 purebred Duroc pig populations (P1 and P2) and their terminal crossbreds [C1 = P1 x (Landrace x Large White) and C2 = P2 x (Landrace x Large White)] raised in different production environments. The traits analyzed were backfat (BF), muscle depth (MD), BW at slaughter (WGT), and weight per day of age (WDA). Data sets from P1, P2, C1, and C2 included 26,674, 8,266, 16,806, and 12,350 animals, respectively. Two-trait models (nucleus and commercial crossbreds) for each group included fixed (contemporary group, sex, weight, and age), random additive (animal for P1 and P2 and sire for C1 and C2), random litter, and random dam (C1 and C2 only) effects. Heritability estimates (+/-SE) for BF were 0.46 +/- 0.04, 0.38 +/- 0.02, 0.32 +/- 0.02, and 0.33 +/- 0.02 for P1, P2, C1, and C2, respectively. Heritability estimates for MD were 0.31 +/- 0.01, 0.23 +/- 0.02, 0.19 +/- 0.01, and 0.12 +/- 0.01 for P1, P2, C1, and C2, respectively. The estimates for WGT and WDA were 0.31 +/- 0.01, 0.21 +/- 0.02, 0.16 +/- 0.01, and 0.18 +/- 0.01 and 0.32 +/- 0.01, 0.22 +/- 0.02, 0.16 +/- 0.01, and 0.19 +/- 0.01, respectively. Genetic correlations between purebreds and crossbreds for BF were 0.83 +/- 0.09 (P1 x C1) and 0.89 +/- 0.05 (P2 x C2), for MD 0.78 +/- 0.05 (P1 x C1) and 0.80 +/- 0.08 (P2 x C2). For WGT and WDA, the correlations were 0.53 +/- 0.08 (P1 x C1), 0.80 +/- 0.10 (P2 x C2), and 0.60 +/- 0.07 (P1 x C1) and 0.79 +/- 0.09 (P2 x C2), respectively. (Co)variances in crossbreds were adjusted to a live BW scale. Compared with purebreds, the genetic variances in crossbreds were lower, and the residual variances were greater. Sire variances in crossbreds were approximately 20 to 30% of the animal variances in purebreds for BF and MD but were 13 to 25% for WGT and WDA. The efficiency of purebred selection on crossbreds, assessed by EBV prediction weights, ranged from 0.43 to 0.91 for line 1 and 0.70 to 0.92 for line 2. When nucleus and commercial environments differ substantially, the efficiency of selection varies by line and traits, and selection strategies that include crossbred data from typical production environments may therefore be desirable.

Animal Husbandry↗

Positive genetic correlation between female preference and offspring fitness.

In many species, females display preferences for extreme male signal traits, but it has not been determined if such preferences evolve as a consequence of females gaining genetic benefits from exercising choice. If females prefer extreme male traits because they indicate male genetic quality that will enhance the fitness of offspring, a genetic correlation will evolve between female preference genes and genes that confer offspring fitness. We show that females of Drosophila serrata prefer extreme male cuticular hydrocarbon (CHC) blends, and that this preference affects offspring fitness. Female preference is positively genetically correlated with offspring fitness, indicating that females have gained genetic benefits from their choice of males. Despite male CHCs experiencing strong sexual selection, the genes underlying attractive CHCs also conferred lower offspring fitness, suggesting a balance between sexual selection and natural selection may have been reached in this population.

Animals↗

Estimates of genetic correlations between testicular measurements and female reproductive traits in cattle.

Data from 528 male and 645 female progeny of 63 sires were used to estimate genetic correlations between female and male reproductive traits. Data were from two Hereford herds involved in a long-term selection program of the North Carolina Agricultural Experiment Service. Testicular measurements of circumference, diameter, length and volume were obtained on bulls at 205 and 365 d. Testicular growth measures were defined as differences between 205-and 365-d measurements. Heifers were placed in the breeding herd as yearlings and given two breeding seasons to produce a calf. Traits utilized from females were three age-at-first-breeding traits, two age-at-first-calving traits, two pregnancy rate traits, rebreeding interval and calving interval. Genetic correlations were estimated from half-sib and from sire-daughter analyses. Seventy-five percent or more of the correlations of testicular measurements with pregnancy rats, age at first breeding and age at first calving were in the favorable direction. Average correlations were .62, -.55 and -.66, respectively. For each of the remaining female traits, approximately 50% of the correlations were favorable and the average correlations were small. Correlations were summarized by testicular measurement with favorable correlations given a negative sign. Testicular diameter had more favorable correlations (80%) than length, volume or circumference (70%). However, average correlations were similar (-.31, -.30, -.34 and -.26, respectively). Testicular measurements taken at either 205 or 365 d had the same percentage of favorable correlations (72%), while testicular growth measurements had a slightly higher percentage of favorable correlations (78%). Average correlations of 365-d measures were higher (-.38) than either 205-d or growth measures (-.25 and -.28, respectively). Heritabilities for testicular measurements tended to be moderate to high, while those for female reproduction tended to be low to moderate. These results suggest that selection for increased testicular size would lead to improvement in female reproduction, particularly an increase in calving rate and a decrease in age at first breeding.

Animals↗

Significant genetic correlations among Caucasians at forensic DNA loci.

Although the effect of population differentiation on the forensic use of DNA profiles has been the subject of controversy for some years now, the debate has largely failed to focus on the genetical questions directly relevant to the forensic context. We re-analyse two published data sets and find that they convey much the same message for forensic inference, in contrast with the dramatically differing conclusions of the original authors. The analysis is likelihood-based and combines information across loci and across populations without assuming constant genetic differentiation. Our results suggest that the relevant genetic correlation coefficients are too large to be ignored in forensic work: although DNA profile evidence is typically very strong, the effect of genetic correlations can be important in some cases. Such correlations can, however, be accommodated in an appropriate assessment of evidential strength so that population genetic issues should not present a barrier to the efficient and fair use of DNA profile evidence.

DNA Fingerprinting↗