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Small for gestational age: short stature and beyond
Paul Saenger1, Paul Czernichow, Ieuan Hughes
1Department of Pediatrics, Albert Einstein College of Medicine, Bronx, New York 10467, USA. PHSaenger@aol.com
Insights
Children born small for gestational age (SGA) face long-term metabolic risks. Early catch-up growth may mitigate these risks, while growth hormone treatment appears safe for those not catching up.
Area of Science:
- Pediatrics
- Endocrinology
- Metabolic Health
Background:
- Up to 10% of neonates are born small for gestational age (SGA).
- SGA infants are at increased risk for later-life metabolic diseases, including insulin resistance, obesity, cardiovascular disease, and type 2 diabetes mellitus.
- Metabolic consequences are often observed in adults who experienced spontaneous catch-up growth in childhood.
Purpose of the Study:
- To explore the long-term metabolic health of individuals born SGA.
- To investigate the impact of catch-up growth and growth hormone (GH) treatment on metabolic outcomes in SGA individuals.
- To evaluate current infant feeding practices in light of SGA-related metabolic risks.
Main Methods:
- Review of existing literature on SGA, catch-up growth, and metabolic disease.
- Analysis of data on the effects of early catch-up growth strategies.
- Examination of recent findings on long-term GH treatment in SGA individuals.
Main Results:
- Early appropriate catch-up growth may mitigate some metabolic consequences of intrauterine growth restriction.
- Excessive weight gain should be avoided in SGA infants.
- Long-term GH treatment in SGA individuals who do not catch up does not appear to increase the risk of type 2 diabetes mellitus or metabolic syndrome in young adulthood.
Conclusions:
- Optimizing early growth in SGA infants is crucial for long-term metabolic health.
- Growth hormone therapy is a potentially safe option for SGA individuals with short stature who do not achieve catch-up growth.
- Further research into infant feeding practices for SGA infants is warranted.
Abstract:
Depending on the definitions used, up to 10% of all live-born neonates are small for gestational age (SGA). Although the vast majority of these children show catch-up growth by 2 yr of age, one in 10 does not. It is increasingly recognized that those who are born SGA are at risk of developing metabolic disease later in life. Reduced fetal growth has been shown to be associated with an increased risk of insulin resistance, obesity, cardiovascular disease, and type 2 diabetes mellitus. The majority of pathology is seen in adults who show spontaneous catch-up growth as children. There is evidence to suggest that some of the metabolic consequences of intrauterine growth retardation in children born SGA can be mitigated by ensuring early appropriate catch-up growth, while avoiding excessive weight gain. Implicitly, this argument questions current infant formula feeding practices. The risk is less clear for individuals who do not show catch-up growth and who are treated with GH for short stature. Recent data, however, suggest that long-term treatment with GH does not increase the risk of type 2 diabetes mellitus and the metabolic syndrome in young adults born SGA.
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