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1.
Artigo em Inglês | MEDLINE | ID: mdl-37897063

RESUMO

BACKGROUND: The way in which socioeconomic status (SES) moderates the etiology of reading attainment has been explored many times, with past work often finding that genetic influences are suppressed under conditions of socioeconomic deprivation and more fully realized under conditions of socioeconomic advantage: a gene-SES interaction. Additionally, past work has pointed toward the presence of gene-location interactions, with the relative influence of genes and environment varying across geographic regions of the same country/state. METHOD: This study investigates the extent to which SES and geographical location interact to moderate the genetic and environmental components of reading attainment. Utilizing data from 2,135 twin pairs in Florida (mean age 13.82 years, range 10.71-17.77), the study operationalized reading attainment as reading comprehension scores from a statewide test and SES as household income. We applied a spatial twin analysis procedure to investigate how twin genetic and environmental estimates vary by geographic location. We then expanded this analysis to explore how the moderating role of SES on said genetic and environmental influences also varied by geographic location. RESULTS: A gene-SES interaction was found, with heritability of reading being suppressed in lower- (23%) versus higher-SES homes (78%). The magnitude of the moderating parameters were not consistent by location, however, and ranged from -0.10 to 0.10 for the moderating effect on genetic influences, and from -0.30 to 0.05 for the moderating effect on environmental influences. For smaller areas and those with less socioeconomic variability, the magnitude of the genetic moderating parameter was high, giving rise to more fully realized genetic influences on reading there. CONCLUSIONS: SES significantly influences reading variability. However, a child's home location matters in both the overall etiology and how strongly SES moderates said etiologies. These results point toward the presence of multiple significant environmental factors that simultaneously, and inseparably, influence the underlying etiology of reading attainment.

2.
Sci Stud Read ; 27(1): 5-20, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36843656

RESUMO

Purpose: Researchers have developed a constellation model of decoding-related reading disabilities (RD) to improve the RD risk determination. The model's hallmark is its inclusion of various RD indicators to determine RD risk. Classification methods such as logistic regression (LR) might be one way to determine RD risk within the constellation model framework. However, some issues may arise with applying the logistic regression method (e.g., multicollinearity). Machine learning techniques, such as random forest (RF), might assist in overcoming these limitations. They can better deal with complex data relations than traditional approaches. We examined the prediction performance of RF and compared it against LR to determine RD risk. Method: The sample comprised 12,171 students from Florida whose third-grade RD risk was operationalized using the constellation model with one, two, three, or four RD indicators in first and second grade. Results: Results revealed that LR and RF performed on par in accurately predicting RD risk. Regarding predictor importance, reading fluency was consistently the most critical predictor for RD risk. Conclusion: Findings suggest that RF does not outperform LR in RD prediction accuracy in models with multiple linearly related predictors. Findings also highlight including reading fluency in early identification batteries for later RD determination.

3.
Dev Sci ; 24(1): e13004, 2021 01.
Artigo em Inglês | MEDLINE | ID: mdl-32524716

RESUMO

Reading and math attainment develop during elementary grades. Questions remain, though, about the co-developmental nature of the relation between reading and math. This study examined dynamic, longitudinal pathways between reading and math in first through fourth grades. Participants of the study were 554 academically at-risk children (Mage at the first assessment point = 6.57 years; SD = 0.38) from Texas Project Achieve. Children were assessed utilizing the Woodcock-Johnson-III reading and math measures. Results from dynamic bivariate latent change score models indicated unidirectional longitudinal coupling effects from reading to math. Specifically, average and high levels of reading performance were associated with subsequent gains in math growth, in particular for below average performing children in math. In contrast, low levels of reading performance had negligible or no amplifying influences on change in math growth. The nature of the dynamics was replicated even when controlling for nonverbal cognitive abilities. Results demonstrated that good reading skills pave the way for children to develop their math skills. Such findings underscore the importance of considering reading performance in treating math difficulties.


Assuntos
Leitura , Instituições Acadêmicas , Aptidão , Criança , Humanos , Matemática
4.
J Child Psychol Psychiatry ; 61(6): 689-698, 2020 06.
Artigo em Inglês | MEDLINE | ID: mdl-31595512

RESUMO

BACKGROUND: Reading is important for children's success in school and beyond, yet many adolescents fail to reach expected levels of proficiency. This highlights the need to better understand the factors that influence reading effectiveness over time, including genes and environment. Greater expression of genetic influence on first- and second-grade reading fluency has been observed in higher quality classroom reading environments. To what degree this early environment continues to influence genetic and other environmental influences on later reading is unknown and was tested in this study. METHODS: The quality of the early classroom reading environment was approximated by gains in oral reading fluency (ORF) across the school year among first- or second-grade classmates of 546 MZ and 1,016 DZ twin children (mean age = 7.13 years; SD = 0.45) who had reading comprehension scores from a state-wide mandatory test in school year 2013-2014 when most twin pairs were in seventh to tenth grade (mean age = 14.41; SD = 1.13) in a variable called Class ORF Gain. Biometrical models were fit to the data to assess whether Class ORF Gain moderated the genetic, shared environmental and/or nonshared environmental variance associated with adolescent reading comprehension. RESULTS: Class ORF Gain moderated shared environmental influences on reading comprehension 6-9 years later. When early classroom reading gains were poor, variability in reading comprehension in adolescence was high and was associated largely with shared environmental influences. When early classroom reading gains were good, overall and shared environmentally influenced variability in adolescent reading comprehension was lower so that genetic influences were most relevant in explaining that variability. CONCLUSIONS: Our findings suggested that classroom reading environment experienced when children were learning to read had a lasting influence on the factors underlying variability in later reading effectiveness.


Assuntos
Compreensão , Interação Gene-Ambiente , Psicologia do Adolescente , Leitura , Gêmeos/genética , Gêmeos/psicologia , Adolescente , Feminino , Humanos , Aprendizagem , Masculino , Instituições Acadêmicas
5.
Child Dev ; 91(5): 1548-1562, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-31732976

RESUMO

The purpose of this study was to test the directionality of influence between reading comprehension (RC) and print exposure (PE), thereby estimating genetic and environmental effects of this relation. The sample consisted of 910 twins in fourth through ninth grades (Mage  = 12.33 years, SD = 1.41) from the Florida Twin Project on Reading, Behavior, and Environment. Using direction-of-causation model in a twin design, results supported a direction of influence running from RC to PE. This relation was underpinned by genetic and environmental factors of RC as well as PE. Implications for reading education are discussed.


Assuntos
Compreensão/fisiologia , Leitura , Gêmeos/psicologia , Adolescente , Livros , Criança , Escolaridade , Feminino , Florida , Humanos , Literatura , Masculino , Meio Social , Gêmeos/genética , Gêmeos/estatística & dados numéricos
6.
Sci Stud Read ; 24(1): 23-56, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32189961

RESUMO

According to the Multiple Deficit Model, comorbidity results when the genetic and environmental risk factors that increase the liability for a disorder are domain-general. In order to explore the role of domain-general etiological risk factors in the co-occurrence of learning-related difficulties, the current meta-analysis compiled 38 studies of third through ninth-grade children to estimate the average genetic, shared environmental, and nonshared environmental correlations between reading and attention-deficit/hyperactivity disorder (ADHD) symptoms, and reading and math, as well as their potential moderators. Results revealed average genetic, shared and nonshared environmental correlations between reading and ADHD symptoms of .42, .64, and .20, and reading and math of .71, .90, and .56, suggesting that reading and math may have more domain-general risk factors than reading and ADHD symptoms. A number of significant sources of heterogeneity were also found and discussed. These results have important implications for both intervention and classification of learning disabilities.

7.
Child Dev ; 89(6): e480-e493, 2018 11.
Artigo em Inglês | MEDLINE | ID: mdl-28569388

RESUMO

This study investigated the etiology of longitudinal relations among kindergarten prereading skills, first-grade word level reading skills, and seventh-grade reading comprehension in 265 monozygotic and 459 dizygotic twin pairs (Mage  = 6.29 years in kindergarten) from the Florida Twin Project on Reading. Using a quadvariate Cholesky decomposition, results showed genetic, shared, and nonshared environmental overlap among prereading skills, word level reading skills, and reading comprehension. In addition, genetic and shared environmental overlap was indicated among word level reading skills and reading comprehension, outside the influence of prereading skills. After accounting for overlapping, there remained moderate genetic and nonshared environmental influence specific to reading comprehension. Implications for reading education are discussed.


Assuntos
Compreensão , Interação Gene-Ambiente , Leitura , Adolescente , Análise de Variância , Criança , Pré-Escolar , Feminino , Florida , Humanos , Estudos Longitudinais , Masculino , Gêmeos
9.
Sci Stud Read ; 22(2): 167-180, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-29527114

RESUMO

A fairly recent definition of reading disability (RD) is that in the form of a hybrid model. The model views RD as a latent construct that is manifested through various observable unexpected impairments in reading related skills and through inadequate response to intervention. The current report evaluated this new conceptualization of RD from an etiological perspective. The sample consisted of 2737 twin pairs in first through fourth grade (Mage = 8.52) from the Florida Twin Project on Reading. Using twin analyses, results showed that a substantial proportion of genetic variance, a small proportion of shared environmental, and a small proportion of non-shared environmental variance was attributed to the RD factor. Findings suggest that the etiological architecture of RD closely mirrors the structure of the hybrid model of RD.

10.
Learn Individ Differ ; 59: 11-21, 2017 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-29276362

RESUMO

Researchers have identified sources of individual differences in writing across beginning and developing writers. The aim of the present study was to further clarify the sources of this variability by investigating the extent to which there are differences in genetic and environmental factors underlying the associations between lexical diversity, syntactic knowledge, and semantic cohesion knowledge in relation to writing. Differences were examined across two developmental phases of writing: beginning (i.e., elementary school) and developing (i.e., middle school). Participants included 262 twin pairs (Mage = 10.88 years) in elementary school and 247 twin pairs (Mage = 13.21 years) in middle school. Twins were drawn from the Florida Twin Project on Reading, Behavior, and Environment. Biometric models were conducted separately for subgroups defined by phase of writing development. Results indicated significant etiological differences in writing components across the two phases, such that effects associated with genes and non-shared environment were greater while effects associated with shared environment were lower in developing writers as compared to beginning writers. Furthermore, results showed that child-specific environment was the largest contributor to individual differences in writing components and their covariation for both beginning and developing writers. These results imply that even direct instruction about writing in schools may be having different effects on children based on their unique experiences.

11.
Sch Psychol ; 39(1): 72-80, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-37155259

RESUMO

Universal screening in reading is a common, and often required, practice in early elementary school. Computer-adaptive screening tools, such as Istation's Indicators of Progress-Early Reading (ISIP-ER), are often chosen for this purpose in schools. In our present study, we examine the validity evidence between the ISIP-ER in kindergarten and third grade State of Texas Assessments of Academic Readiness (STAAR) reading scores, the classification accuracy of ISIP-ER to predict which students will meet STAAR reading expectations, and a cut score to maximize classification accuracy for the local context. The sample included 962 students (Mage = 6.19 years; SDage = 0.37) from 15 elementary schools in one suburban school district in Texas. As for validity, the correlation between ISIP-ER in kindergarten and the third grade STAAR was moderate (r = 0.48). Classification accuracy analyses using the vendor-recommended cut score found sensitivity (0.63) and specificity (0.70) were all below recommended levels. Using a locally determined cut score, sensitivity (0.92) was improved, but specificity (0.33) was substantially decreased. The findings suggest ISIP-ER has some limitations in the accurate identification of students at risk for poor outcomes on a state-mandated reading test and will likely need to be combined with other assessments or progress monitoring data. (PsycInfo Database Record (c) 2024 APA, all rights reserved).


Assuntos
Leitura , Instituições Acadêmicas , Humanos , Criança , Lactente , Estudantes
12.
J Learn Disabil ; 55(3): 242-253, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-33899570

RESUMO

Research on the question of creative benefit accompanying dyslexia has produced conflicting findings. In this meta-analysis, we determined summary effects of mean and variance differences in creativity between groups with and without dyslexia. Twenty studies were included (n = 770 individuals with dyslexia, n = 1,671 controls). A random-effects robust variance estimation (RVE) analysis indicated no mean (g = -0.02, p = .84) or variance (g = -0.0004, p = .99) differences in creativity between groups. The mean summary effect was moderated by age, gender, and creativity domain. Compared with adolescents, adults with dyslexia showed an advantage over nondyslexic adults in creativity. In addition, a higher proportion of males in the dyslexia group was associated with poorer performance compared with the controls. Finally, the dyslexia group showed a significant performance disadvantage in verbal versus figural creativity. Regarding variance differences, they varied across age and creativity domains. Compared with adults, adolescents showed smaller variability in the dyslexia group. If the creativity task measured verbal versus figural or combined creativity, the dyslexia group exhibited smaller variability. Altogether, our results suggest that individuals with dyslexia as a group are no more creative or show greater variability in creativity than peers without dyslexia.


Assuntos
Dislexia , Adolescente , Adulto , Criatividade , Humanos , Masculino
13.
Neurosci Biobehav Rev ; 132: 465-494, 2022 01.
Artigo em Inglês | MEDLINE | ID: mdl-34856223

RESUMO

Behavioral research supports the efficacy of intervention for reading disability, but the brain mechanisms underlying improvement in reading are not well understood. Here, we review 39 neuroimaging studies of reading intervention to characterize links between reading improvement and changes in the brain. We report evidence of changes in activation, connectivity, and structure within the reading network, and right hemisphere, frontal and sub-cortical regions. Our meta-analysis of changes in brain activation from pre- to post- reading intervention in eight studies did not yield any significant effects. Methodological heterogeneity among studies may contribute to the lack of significant meta-analytic findings. Based on our qualitative synthesis, we propose that brain changes in response to intervention should be considered in terms of interactions among distributed cognitive, linguistic and sensory systems, rather than via a "normalized" vs. "compensatory" dichotomy. Further empirical research is needed to identify effects of moderating factors such as features of intervention programs, neuroimaging tasks, and individual differences among participants.


Assuntos
Mapeamento Encefálico , Dislexia , Encéfalo/diagnóstico por imagem , Encéfalo/fisiologia , Dislexia/diagnóstico por imagem , Dislexia/terapia , Humanos , Imageamento por Ressonância Magnética , Plasticidade Neuronal
14.
Brain Sci ; 12(1)2021 Dec 26.
Artigo em Inglês | MEDLINE | ID: mdl-35053771

RESUMO

Dyslexia, a specific reading disability, is a common (up to 10% of children) and highly heritable (~70%) neurodevelopmental disorder. Behavioral and molecular genetic approaches are aimed towards dissecting its significant genetic component. In the proposed review, we will summarize advances in twin and molecular genetic research from the past 20 years. First, we will briefly outline the clinical and educational presentation and epidemiology of dyslexia. Next, we will summarize results from twin studies, followed by molecular genetic research (e.g., genome-wide association studies (GWASs)). In particular, we will highlight converging key insights from genetic research. (1) Dyslexia is a highly polygenic neurodevelopmental disorder with a complex genetic architecture. (2) Dyslexia categories share a large proportion of genetics with continuously distributed measures of reading skills, with shared genetic risks also seen across development. (3) Dyslexia genetic risks are shared with those implicated in many other neurodevelopmental disorders (e.g., developmental language disorder and dyscalculia). Finally, we will discuss the implications and future directions. As the diversity of genetic studies continues to increase through international collaborate efforts, we will highlight the challenges in advances of genetics discoveries in this field.

15.
J Learn Disabil ; 52(2): 135-145, 2019.
Artigo em Inglês | MEDLINE | ID: mdl-29790411

RESUMO

A risk to develop a learning disability has been shown to run in families. Having a positive family history of learning disability seems to account for mean differences in achievement outcomes (reading, math) in that children with a positive family history score significantly lower compared to their peers with no such family history. However, the role of family history status in explaining etiological (genetic and environmental) differences among these subgroups of children has yet to be established. The present study of 872 twins (Mage = 13.30, SDage = 1.40) from the Florida Twin Project on Reading, Behavior, and Environment utilized a multigroup approach to examine etiological differences on reading, spelling, and math among two subgroups defined by family history status. Results showed significant mean differences on all achievement outcomes, aside from math; however, no significant etiological differences on any achievement outcome were found among the two subgroups. Results support previous literature that the risk for developing a learning disability is transmitted through a family, but this is seemingly not manifested by differential etiology.


Assuntos
Sucesso Acadêmico , Família , Deficiências da Aprendizagem/etiologia , Deficiências da Aprendizagem/genética , Adolescente , Criança , Suscetibilidade a Doenças , Feminino , Interação Gene-Ambiente , Humanos , Masculino
16.
J Vis Exp ; (151)2019 09 17.
Artigo em Inglês | MEDLINE | ID: mdl-31609333

RESUMO

The Cholesky decomposition method is the gold standard used in the field of behavioral genetics. The method is popular because it is easy to program and solve. Using this method, researchers can explore individual differences in longitudinal relations of different variables across multiple time points. The method allows investigators to decompose variance into (1) unique genetic, shared and non-shared environmental effects that arise at specific time points as well as (2) overlapping genetic, shared and non-shared environmental effects that carry over from one time point to another. However, the method does not identify the mechanisms or origins underlying these effects. The current report focuses on application of the Cholesky decomposition method in the field of educational psychology. Specifically, it discusses individual differences in longitudinal relations between kindergarten letter knowledge, kindergarten phonological awareness, first grade word-level reading skills, and seventh grade reading comprehension.


Assuntos
Genética Comportamental/métodos , Individualidade , Leitura , Criança , Feminino , Humanos , Estudos Longitudinais , Masculino , Fonética
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