Pediatric endocrinology

Serum DLK1 During Minipuberty and Pubertal Transition in Healthy Girls and in Girls With Precocious Puberty

J Clin Endocrinol MetabPublished Longitudinal cohort study

Authors' conclusion

Circulating DLK1 levels declined steeply during infancy and were less pronounced through pubertal development. Due to considerable interindividual variation, DLK1 is not useful as a diagnostic marker of pubertal onset. Importantly, DLK1 was negatively associated with birth weight and body fat percentage.

Study context

Population
Healthy infant girls, healthy peripubertal girls and girls with central precocious puberty (CPP) treated with gonadotropin-releasing hormone agonist (GnRHa)
Participants
85 / 15 / 15
Exposure
Healthy infant girls vs Healthy peripubertal girls vs CPP
  • Healthy infant girlsn = 85
  • Healthy peripubertal girlsn = 15
  • CPPn = 15
Outcome
Longitudinal changes in circulating DLK1 concentrations (ELISA)
Methodological detailsthree longitudinal studies, Body fat percentage calculated using the Slaughter equation
  • Three longitudinal studies
  • Body fat percentage calculated using the Slaughter equation

Main finding

As reported in the abstract

Serum DLK1
Healthy infant girls: DLK1 declined through first year of life
17.6 to 9.9 ng/mL, P = .020
Healthy infant girls: DLK1 inversely correlated with birth weight
r = −0.220, P = .044
Healthy infant girls: DLK1 inversely correlated with BF%
r = −0.503, P < .001
Healthy peripubertal girls: DLK1 declined from 1 year before pubertal onset to first examination after onset
10.4 to 9.2 ng/mL, P = .004
Healthy peripubertal girls: DLK1 declined from 1 year before pubertal onset to last pubertal evaluation
10.4 to 9.8 ng/mL, P = .006

Observational data: associations, not effects.

Original publication

Serum DLK1 During Minipuberty and Pubertal Transition in Healthy Girls and in Girls With Precocious Puberty. J Clin Endocrinol Metab. Published 28 October 2024. doi:10.1210/clinem/dgae762

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