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Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort
Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort
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Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort
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Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort
Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort

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Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort
Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort
Journal Article

Associations of four biological age markers with child development: A multi-omic analysis in the European HELIX cohort

2023
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Overview
Although age is generally measured by the number of years since birth, many factors contribute to the rate at which a person physically ages. In adults, linking these measurements to age gives a measure of overall health and resilience. This ‘biological age’ offers a better prediction of remaining life and disease risk than the number of years lived. Multiple factors can be used to calculate biological age, such as measuring the length of telomeres – protective caps on the end of chromosomes – which shorten as people age. The rate at which they shorten can give an indication of how quickly someone is ageing. Researchers can also study epigenetic factors: these mechanisms lead to certain genes being switched on or off, and they can be combined into a ‘epigenetic clock’ to assess biological age. However, compared with adults, the relationship between biological age and child health and developmental maturity is less well understood. Robinson et al. studied 1,173 school-aged children from six European countries, measuring telomere length, epigenetic factors and other biological indicators related to metabolism and the immune system. The relationships between these factors and an array of child developmental measures such as height, weight, behaviour and the age of onset of puberty were established. The findings showed that biological age indicators are only weakly linked to each other in children. Despite this, biological age was related to greater amount of body fat across all tested indicators – which is also associated with biological age in adults and is an important determinant of lifespan. Among several observed effects on development, analysis found that shorter telomere length and older epigenetic age were associated with greater behavioural problems, suggesting they may be detrimental to child development. On the other hand, a greater age due to metabolic and immune related changes was associated with greater cognitive and behavioural maturity. Environmental factors were also linked to biological ageing, with children exposed to smoking in their homes or while their mother was pregnant displaying an older epigenetic age. Robinson et al. showed that biological ageing in children is multifaceted and can have both beneficial and harmful impacts on development. This knowledge is important for identifying early life risk factors that might influence healthy ageing in later life. Future work will help researchers to understand these complex interactions and the long-term consequences for health and well-being.