scholarly journals On the Importance of Early-Life Cognitive Abilities in Shaping Later-Life Outcomes

2014 ◽  
Vol 11 (3) ◽  
pp. 241-246 ◽  
Author(s):  
Scott M. Hofer ◽  
Sean Clouston
2020 ◽  
Author(s):  
Doretta Caramaschi ◽  
Alexander Neumann ◽  
Andres Cardenas ◽  
Gwen Tindula ◽  
Silvia Alemany ◽  
...  

ABSTRACTCognitive skills are a strong predictor of a wide range of later life outcomes. Genetic and epigenetic associations across the genome explain some of the variation in general cognitive abilities in the general population and it is plausible that epigenetic associations might arise from prenatal environmental exposures and/or genetic variation early in life. We investigated the association between cord blood DNA methylation at birth and cognitive skills assessed in children from eight pregnancy cohorts (N=2196-3798) within the Pregnancy And Childhood Epigenetics (PACE) Consortium across overall, verbal and non-verbal cognitive scores. The associations at single CpG sites were weak for all of the cognitive domains investigated. One region near DUSP22 on chromosome 6 was associated with non-verbal cognition in a model adjusted for maternal IQ. We conclude that there is little evidence to support the idea that cord blood DNA methylation at single CpGs can predict cognitive skills and further studies are needed to confirm regional differences.


2020 ◽  
Author(s):  
Ellen Verhoef ◽  
Chin Yang Shapland ◽  
E. Fisher Simon ◽  
Philip S. Dale ◽  
Beate St Pourcain

AbstractIndividual differences in early-life vocabulary measures are heritable and associated with subsequent reading and cognitive abilities, although the underlying mechanisms are little understood. Here, we (i) investigate the developmental genetic architecture of expressive and receptive vocabulary in toddlerhood and (ii) assess origin and developmental stage of emerging genetic associations with mid-childhood verbal and non-verbal skills.Studying up to 6,524 unrelated children from the population-based Avon Longitudinal Study of Parents and Children (ALSPAC) cohort, we dissected the phenotypic variance of longitudinally assessed early-life vocabulary measures (15-38 months) and later-life reading and cognitive skills (7-8 years) into genetic and residual components, by fitting multivariate structural equation models to genome-wide genetic-relationship matrices.Our findings show that the genetic architecture of early-life vocabulary is dynamic, involving multiple distinct genetic factors. Two of them are developmentally stable and contribute to genetic variation in mid-childhood skills: Genetic links with later-life verbal abilities (reading, verbal intelligence) emerged with expressive vocabulary at 24 months. The underlying genetic factor explained 10.1% variation (path coefficient: 0.32(SE=0.06)) in early language, but also 6.4% (path coefficient: 0.25(SE=0.12)) and 17.9% (path coefficient: 0.42(SE=0.13)) variation in mid-childhood reading and verbal intelligence, respectively. An independent stable genetic factor was identified for receptive vocabulary at 38 months, explaining 2.1% (path coefficient: 0.15(SE=0.07)) phenotypic variation. This genetic factor was also linked to both verbal and non-verbal cognitive abilities in mid-childhood, accounting for 24.7% of the variation in non-verbal intelligence (path coefficient: 0.50(SE=0.08)), 33.0% in reading (path coefficient: 0.57(SE=0.07)) and 36.1% in verbal intelligence (path coefficient: 0.60(0.10)), corresponding to the majority of genetic variance (≥66.4%).Thus, the genetic foundations of mid-childhood reading and cognition are diverse. They involve at least two independent genetic factors that emerge at different developmental stages during early language development and may implicate differences in cognitive processes that are already detectable during toddlerhood.Author summaryDifferences in the number of words young children produce (expressive vocabulary) and understand (receptive vocabulary) can be partially explained by genetic factors, and are related to reading and cognitive abilities later in life. Here, we studied genetic influences underlying word production and understanding during early development (15-38 months) and their genetic relationship with mid-childhood reading and cognitive skills (7-8 years), based on longitudinal phenotype measures and genome-wide genetic data from up to 6,524 unrelated children. We showed that vocabulary skills assessed at different stages during early development are influenced by distinct genetic factors, two of which also contribute to genetic variation in mid-childhood skills, suggesting developmental stability: Genetic sources emerging for word production skills at 24 months were linked to subsequent verbal abilities, including mid-childhood reading and verbal intelligence performance. A further independent genetic factor was identified that related to word comprehension at 38 months and also contributed to variation in later verbal as well as non-verbal abilities during mid-childhood. Thus, the genetic foundations of mid-childhood reading and cognition involve at least two independent genetic factors that emerge during early-life langauge development and may implicate differences in overarching cognitive mechanisms.


2012 ◽  
Vol 120 (10) ◽  
pp. 1353-1361 ◽  
Author(s):  
Kim Boekelheide ◽  
Bruce Blumberg ◽  
Robert E. Chapin ◽  
Ila Cote ◽  
Joseph H. Graziano ◽  
...  

2015 ◽  
Vol 100 (11) ◽  
pp. 1058-1063 ◽  
Author(s):  
Thomas C Williams ◽  
Amanda J Drake

The process whereby early exposure to an adverse environment has an influence on later life outcomes has been called ‘early life programming’. While epidemiological evidence for this has been available for decades, only in recent years have the mechanisms, in particular epigenetic modifications, for this process begun to be elucidated. We discuss the evidence for early life programming, the possible mechanisms, how effects may be transmitted across generations, and conclude by looking at some examples relevant to general paediatrics.


PLoS Genetics ◽  
2021 ◽  
Vol 17 (2) ◽  
pp. e1009144
Author(s):  
Ellen Verhoef ◽  
Chin Yang Shapland ◽  
Simon E. Fisher ◽  
Philip S. Dale ◽  
Beate St Pourcain

Individual differences in early-life vocabulary measures are heritable and associated with subsequent reading and cognitive abilities, although the underlying mechanisms are little understood. Here, we (i) investigate the developmental genetic architecture of expressive and receptive vocabulary in early-life and (ii) assess timing of emerging genetic associations with mid-childhood verbal and non-verbal skills. We studied longitudinally assessed early-life vocabulary measures (15–38 months) and later-life verbal and non-verbal skills (7–8 years) in up to 6,524 unrelated children from the population-based Avon Longitudinal Study of Parents and Children (ALSPAC) cohort. We dissected the phenotypic variance of rank-transformed scores into genetic and residual components by fitting multivariate structural equation models to genome-wide genetic-relationship matrices. Our findings show that the genetic architecture of early-life vocabulary involves multiple distinct genetic factors. Two of these genetic factors are developmentally stable and also contribute to genetic variation in mid-childhood skills: One genetic factor emerging with expressive vocabulary at 24 months (path coefficient: 0.32(SE = 0.06)) was also related to later-life reading (path coefficient: 0.25(SE = 0.12)) and verbal intelligence (path coefficient: 0.42(SE = 0.13)), explaining up to 17.9% of the phenotypic variation. A second, independent genetic factor emerging with receptive vocabulary at 38 months (path coefficient: 0.15(SE = 0.07)), was more generally linked to verbal and non-verbal cognitive abilities in mid-childhood (reading path coefficient: 0.57(SE = 0.07); verbal intelligence path coefficient: 0.60(0.10); performance intelligence path coefficient: 0.50(SE = 0.08)), accounting for up to 36.1% of the phenotypic variation and the majority of genetic variance in these later-life traits (≥66.4%). Thus, the genetic foundations of mid-childhood reading and cognitive abilities are diverse. They involve at least two independent genetic factors that emerge at different developmental stages during early language development and may implicate differences in cognitive processes that are already detectable during toddlerhood.


2019 ◽  
Author(s):  
Tyler W. Watts ◽  
Greg J. Duncan

Longitudinal studies of development often rely on correlational methods to examine linkages between early-life constructs and later-life outcomes. As highlighted by responses to our article, “Revisiting the Marshmallow Test: A Conceptual Replication Investigating Links Between Delay of Gratification and Later Outcomes,” interpretations of these linkages can be difficult. In this commentary, we address criticisms that our approach “over-controlled” for key factors related to a child’s ability to delay gratification, allay concerns over multicollinearity, and discuss how multivariate regression techniques can help clarify the interpretation of observed predictive relations.


2021 ◽  
pp. 002214652110054
Author(s):  
Sarah A. Mustillo ◽  
Miao Li ◽  
Patricia Morton ◽  
Kenneth F. Ferraro

Prior research reveals that negative early-life experiences play a major role in the development of obesity in later life, but few studies identify mechanisms that alter the lifetime risk of obesity. This study examines the influence of negative childhood experiences on body mass index (BMI) and obesity (BMI ≥30) during older adulthood and the psychosocial and behavioral pathways involved. Using a nationally representative sample, we examine the influence of cumulative misfortune as well as five separate domains of misfortune on BMI and obesity. Results show that four of the five domains are associated with BMI and obesity either directly, indirectly, or both. The influence of cumulative misfortune on the outcomes is mediated by three adult factors: socioeconomic status, depressive symptoms, and physical activity. The mediators identified here provide targets for intervention among older adults to help offset the health risks of excess BMI attributable of early-life exposure to misfortune.


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