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The same growth pattern from puberty suggests that modern human diversity results from changes during pre-pubertal development.

ABSTRACT: Patterns of human growth established for one population have rarely been tested in other populations. In a previous study, three growth curves from puberty were modelled for each sex in a longitudinal study of a Caucasian population based on stature, age at peak of growth and biological maturation. Each curve represents the canalisation of growth associated with the type of puberty. The high precision (±?3 cm) of individual adult stature predictions shows that growth kinetics are already set up at puberty and are canalised depending on biological maturity. Our aim is to assess whether this model can be extrapolated to other populations to test whether growth canalisation is a population-dependent phenomenon or if the model reflects a canalisation pattern specific to our species. The modelled curves predicted adult stature with the same high degree of precision in basketball players and the Baka pygmies. Therefore, (1) the relationship between growth kinetics and age at maturity is similar in all populations and (2) growth according to pubertal stages follows the same canalisation patterns in the populations despite the wide differences in their average adult statures. It suggests that morphological diversity in modern humans results from processes taking place in early development.

SUBMITTER: Pineau JC

PROVIDER: S-EPMC7921106 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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The same growth pattern from puberty suggests that modern human diversity results from changes during pre-pubertal development.

Pineau Jean-Claude JC Ramirez Rozzi Fernando V FV

Scientific reports 20210301 1

Patterns of human growth established for one population have rarely been tested in other populations. In a previous study, three growth curves from puberty were modelled for each sex in a longitudinal study of a Caucasian population based on stature, age at peak of growth and biological maturation. Each curve represents the canalisation of growth associated with the type of puberty. The high precision (± 3 cm) of individual adult stature predictions shows that growth kinetics are already set up ...[more]

PMID: 33649394

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Project description:BackgroundAdolescence is a period characterized by major biological development, which may be associated with changes in DNA methylation (DNA-M). However, it is unknown to what extent DNA-M varies from pre- to post-adolescence, whether the pattern of changes is different between females and males, and how adolescence-related factors are associated with changes in DNA-M.MethodsGenome-scale DNA-M at ages 10 and 18 years in whole blood of 325 subjects (n = 140 females) in the Isle of Wight (IOW) birth cohort was analyzed using Illumina Infinium arrays (450K and EPIC). Linear mixed models were used to examine DNA-M changes between pre- and post-adolescence and whether the changes were gender-specific. Adolescence-related factors and environmental exposure factors were assessed on their association with DNA-M changes. Replication of findings was attempted in the comparable Avon Longitudinal Study of Parents and Children (ALSPAC) cohort.ResultsIn the IOW cohort, after controlling for technical variation and cell compositions at both pre- and post-adolescence, 15,532 cytosine-phosphate-guanine (CpG) sites (of 400,825 CpGs, 3.88%) showed statistically significant DNA-M changes from pre-adolescence to post-adolescence invariant to gender (false discovery rate (FDR) = 0.05). Of these 15,532 CpGs, 10,212 CpGs (66%) were replicated in the ALSPAC cohort. Pathway analysis using Ingenuity Pathway Analysis (IPA) identified significant biological pathways related to growth and development of the reproductive system, emphasizing the importance of this period of transition on epigenetic state of genes. In addition, in IOW, we identified 1179 CpGs with gender-specific DNA-M changes. In the IOW cohort, body mass index (BMI) at age 10 years, age of growth spurt, nonsteroidal drugs use, and current smoking status showed statistically significant associations with DNA-M changes at 15 CpGs on 14 genes such as the AHRR gene. For BMI at age 10 years, the association was gender-specific. Findings on current smoking status were replicated in the ALSPAC cohort.ConclusionAdolescent transition is associated with changes in DNA-M at more than 15K CpGs. Identified pathways emphasize the importance of this period of transition on epigenetic state of genes relevant to cell growth and immune system development.

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The same growth pattern from puberty suggests that modern human diversity results from changes during pre-pubertal development.

Publications

The same growth pattern from puberty suggests that modern human diversity results from changes during pre-pubertal development.

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