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Determination of Reproductive Competence by Confirming Pubertal Onset and Performing a Fertility Assay in Mice and Rats
Published on: October 13, 2018
Puberty and prenatal growth
Lourdes Ibáñez1, Francis de Zegher
1Endocrinology Unit, Hospital Sant Joan de Déu, University of Barcelona, Passeig de Sant Joan de Déu 2, 08950 Esplugues, Barcelona, Spain. libanez@hsjdbcn.org
Insights
Children born small-for-gestational-age (SGA) experience altered puberty. Insulin resistance may drive early puberty in SGA girls, suggesting insulin sensitization as a potential intervention.
Area of Science:
- Pediatric Endocrinology
- Reproductive Health
- Developmental Biology
Background:
- Prenatal growth restriction, indicated by being born small-for-gestational-age (SGA), is increasingly linked to pubertal development.
- Children born SGA exhibit distinct pubertal trajectories compared to their peers.
Purpose of the Study:
- To review pubertal characteristics in children born small-for-gestational-age (SGA).
- To explore potential mechanisms, such as insulin resistance, linking SGA status to altered pubertal timing.
- To discuss therapeutic implications for managing pubertal issues in SGA individuals.
Main Methods:
- Review of existing literature on pubertal development in children born small-for-gestational-age (SGA).
- Analysis of hormonal profiles (FSH, inhibin B) and physical characteristics (testicular volume, genitalia size) in SGA populations.
- Examination of the impact of insulin-sensitizing therapy on ovulation rates in SGA adolescents.
Main Results:
- Boys born SGA may have elevated FSH, low inhibin B, and smaller testicular volume during adolescence.
- Girls born SGA tend to experience earlier pubertal onset and menarche (by 5-10 months), with potential associations with higher FSH and smaller internal genitalia.
- SGA adolescents exhibit reduced ovulation rates, which can be improved with insulin-sensitizing therapy.
- Precocious pubarche in SGA girls is associated with advanced menarche, potentially mediated by insulin resistance.
Conclusions:
- Prenatal growth restriction impacts pubertal development in both boys and girls born SGA.
- Insulin resistance is a likely mechanism connecting the post-SGA state to early menarche in girls.
- Insulin sensitization presents a promising therapeutic strategy to prevent early menarche and growth arrest in SGA girls.
Abstract:
There is increasing evidence for a link between puberty and prenatal growth. Here we highlight a selection of pubertal characteristics in children who were born small-for-gestational-age (SGA). Boys born SGA are at risk for high FSH and low inhibin B levels, and a small testicular volume in adolescence. In girls born SGA, the age at pubertal onset and the age at menarche are advanced by about 5-10 months; prenatal growth restraint may be associated with higher FSH levels and with small internal genitalia in adolescence. The ovulation rate was found to be low in SGA adolescents, and an insulin-sensitizing therapy was capable of raising this low ovulation rate. Menarche is definitely advanced in SGA girls with precocious pubarche. Current evidence suggests that insulin resistance is a key mechanism linking a post-SGA state to early menarche; hence, insulin sensitization may become a valid approach to prevent early menarche and early growth arrest in SGA girls.
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