Intrauterine growth restriction: no unifying risk factor for the metabolic syndrome in young adults
Anne M Euser1, Friedo W Dekker, Stein I Hallan
1Department of Cancer Research and Molecular Medicine, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Insights
Low birth weight was not linked to metabolic syndrome in young adults. While some birth weight associations with individual metabolic syndrome components were observed, they were inconsistent and did not translate to an overall syndrome risk.
Area of Science:
- Cardiovascular Health
- Metabolic Disorders
- Perinatal Medicine
Background:
- The metabolic syndrome's role as a cardiovascular risk factor is debated due to unclear pathophysiology.
- Intrauterine growth retardation (low birth weight) is a potential risk factor for cardiovascular issues and metabolic syndrome.
Purpose of the Study:
- To investigate the association between intrauterine growth retardation and the metabolic syndrome in young adults.
- To determine if low birth weight predicts metabolic syndrome components or the overall syndrome.
Main Methods:
- Utilized data from the population-based HUNT 2 study (n=7435) of individuals aged 20-30 years.
- Employed logistic regression with fractional polynomial models to analyze the relationship between birth weight and metabolic syndrome.
- Included data from the Norwegian Medical Birth Registry for intrauterine growth retardation assessment.
Main Results:
- In men, low birth weight showed associations with central obesity, raised triglycerides, reduced HDL-cholesterol, raised blood pressure, and impaired glucose tolerance.
- In women, associations were found with central obesity and raised blood pressure, but not other components.
- An association between low birth weight and the metabolic syndrome was only observed in men (exponentially, with higher risk in high birth weight individuals), but not in women.
Conclusions:
- Low birth weight was not associated with the metabolic syndrome in young adulthood.
- Specific components of the metabolic syndrome showed varied associations with birth weight, with differing directions in men and women.
Background:
The validity and appropriateness of the metabolic syndrome as a cardiovascular risk factor are increasingly debated, partly because of the lack of a unifying underlying pathophysiological mechanism. Intrauterine growth retardation (low birth weight by sex and gestational length) has been associated with several cardiovascular problems and could be an important underlying risk factor for the metabolic syndrome.
Methods:
The association between intrauterine growth retardation (from the Norwegian Medical Birth Registry) and the metabolic syndrome in 7435 men and women aged 20-30 years from the population-based HUNT 2 study was studied with logistic regression using fractional polynomial models.
Results:
In men, there were significant associations with several of the separate components of the metabolic syndrome: central obesity (exponential, P<0.001), raised triglycerides (negative linear, P = 0.018), reduced HDL-cholesterol (U-shaped, P = 0.086), raised blood pressure (negative linear, P = 0.036), and impaired glucose tolerance (negative linear, P = 0.036). In women, there were significant associations with central obesity (positive linear, P<0.001) and raised blood pressure (negative linear, P = 0.003) but not with the other components. When combining these components into the metabolic syndrome, an exponential association was found in men (P = 0.017), that is, increased risk in patients with high birth weight only. In women, there was no association at all (P = 0.959).
Conclusion:
Low birth weight was not associated with the metabolic syndrome at young adult age. Several associations between birth weight and the separate components of the syndrome were found, however, but these associations were partly in different directions.
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