Growth patterns during childhood and the relationship with acylation-stimulating protein
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Updated: Jun 16, 2026

Acyl-PEGyl Exchange Gel Shift Assay for Quantitative Determination of Palmitoylation of Brain Membrane Proteins
Published on: March 29, 2020
R W J Leunissen1, Y Gao, K Cianflone
1Department of Pediatrics, Subdivision of Endocrinology, Erasmus MC/Sophia Children's Hospital, Rotterdam, the Netherlands. r.leunissen@erasmusmc.nl
Insights
Exaggerated weight gain in childhood, not fetal growth, impacts Acylation-stimulating protein (ASP) levels and may impair free fatty acid (FFA) uptake. Preventing excessive childhood weight gain is crucial for metabolic health.
Area of Science:
- Endocrinology
- Metabolic Health
- Human Growth and Development
Background:
- Acylation-stimulating protein (ASP) is an adipose-derived hormone regulating glucose and free fatty acid (FFA) uptake.
- Altered ASP metabolism is linked to lipid metabolism changes.
- Postnatal catch-up growth is associated with later-life dyslipidemia.
Purpose of the Study:
- To investigate the association between ASP levels and birth size, adult size, and childhood growth patterns.
- To explore the role of postnatal growth in ASP metabolism and lipid regulation.
Main Methods:
- Multiple regression analyses were performed on 285 young adults (aged 18-24).
- ASP levels were compared across subgroups: small for gestational age with short stature (SGA-S), small for gestational age with catch-up growth (SGA-CU), idiopathic short stature (ISS), and controls.
Main Results:
- Childhood weight gain, especially fat accumulation, positively correlated with early adulthood ASP levels, independent of birth size, age, and gender.
- Foetal growth (birth size) showed no relation to ASP levels.
- No significant differences in ASP levels were found between subgroups, but SGA-CU and ISS groups had higher FFA levels.
Conclusions:
- Exaggerated childhood weight gain, not fetal growth, influences ASP metabolism.
- Altered ASP metabolism may lead to impaired FFA uptake and delayed triglyceride clearance.
- Preventing exaggerated weight gain during childhood is recommended to mitigate metabolic alterations.
Background/Objectives:
Acylation-stimulating protein (ASP) is an adipose tissue-derived hormone, which stimulates glucose and free fatty acid (FFA) uptake into adipocytes. Changes in ASP metabolism are associated with alterations in lipid metabolism. As postnatal catch-up growth has been associated with dyslipidaemia in later life, we investigated the association between ASP and birth size, adult size and different growth patterns during childhood.
Methods:
The associations were investigated by multiple regression analyses in 285 young adults, aged 18-24. Subsequently, differences in ASP were analysed in four clinically relevant subgroups, young adults either born small for gestational age with short stature (SGA-S) or with catch-up growth (SGA-CU), or born appropriate for gestational age with idiopathic short stature (ISS) or with normal stature (controls).
Results:
Weight gain during childhood, particularly fat accumulation, was positively related to ASP levels in early adulthood, independent of birth size, age and gender. Foetal growth, reflected by birth size, was not related to ASP levels. Between the subgroups, no differences in ASP were found, but SGA-CU and ISS subjects had significantly higher levels of FFA.
Conclusion:
Exaggerated weight gain during childhood, but not foetal growth, contributes to alterations in ASP metabolism, which may be associated with impaired FFA uptake and delayed triglycerides clearance. Therefore, exaggerated weight gain during childhood should be prevented.
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