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. 2019 Mar;34(3):279-300.
doi: 10.1007/s10654-019-00502-9. Epub 2019 Mar 18.

The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects

Collaborators, Affiliations

The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects

Christel M Middeldorp et al. Eur J Epidemiol. 2019 Mar.

Abstract

The impact of many unfavorable childhood traits or diseases, such as low birth weight and mental disorders, is not limited to childhood and adolescence, as they are also associated with poor outcomes in adulthood, such as cardiovascular disease. Insight into the genetic etiology of childhood and adolescent traits and disorders may therefore provide new perspectives, not only on how to improve wellbeing during childhood, but also how to prevent later adverse outcomes. To achieve the sample sizes required for genetic research, the Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia were established. The majority of the participating cohorts are longitudinal population-based samples, but other cohorts with data on early childhood phenotypes are also involved. Cohorts often have a broad focus and collect(ed) data on various somatic and psychiatric traits as well as environmental factors. Genetic variants have been successfully identified for multiple traits, for example, birth weight, atopic dermatitis, childhood BMI, allergic sensitization, and pubertal growth. Furthermore, the results have shown that genetic factors also partly underlie the association with adult traits. As sample sizes are still increasing, it is expected that future analyses will identify additional variants. This, in combination with the development of innovative statistical methods, will provide detailed insight on the mechanisms underlying the transition from childhood to adult disorders. Both consortia welcome new collaborations. Policies and contact details are available from the corresponding authors of this manuscript and/or the consortium websites.

Keywords: Childhood traits and disorders; Consortium; Genetics; Longitudinal.

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Figures

Fig. 1
Fig. 1
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Fig. 2
Fig. 2
Genome-wide genetic correlation between birth weight and a range of traits and diseases in later life. Genome-wide genetic correlations between birth weight and traits and diseases evaluated in later life. The figure (adapted from Horikoshi et al. 2016 [28] with permission of the authors) displays the genetic correlations between birth weight and a range of traits and diseases in later life as estimated using LD Score regression. Traits selected were those for which genome-wide association summary statistics were available in suitably large sample sizes, and the analyses were typically performed on the largest meta-analyses available as of early 2016. The genetic correlation estimates (rg) are colour coded according to phenotypic area. Allelic direction of effect is aligned to increased birth weight. Size of the circle denotes the significance level for the correlation (per the key). Correlations with a lower significance level are not depicted. Further detail on the methods and studies involved is available in Horikoshi et al. 2016 [28]. Diameter of circles is proportional to genetic correlation p value

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