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Published on: June 29, 2013
The cortisol-cortisone shuttle in children born with intrauterine growth retardation
M Houang1, G Morineau, Y le Bouc
1Laboratoire d'Explorations Fonctionnelles Endocriniennes, Hopital Trousseau AP-HP, Paris, France.
Insights
Twenty percent of children with intrauterine growth retardation (IUGR) and poor growth exhibit elevated cortisol/cortisone ratios, suggesting a potential 11beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2) deficit. This may link IUGR to later health issues.
Area of Science:
- Endocrinology
- Pediatrics
- Developmental Biology
Background:
- Intrauterine growth retardation (IUGR) is linked to nephron deficit and increased risk of cardiovascular diseases, hypertension, glucose intolerance, and dyslipidemia.
- The enzyme 11beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2), primarily in the kidney, plays a crucial role in regulating cortisol levels; its deficit can lead to hypertension.
Purpose of the Study:
- To investigate the potential involvement of 11beta-HSD2 dysfunction in the poor growth rates of children born with IUGR.
- To assess the relationship between cortisol/cortisone (F/E) ratios and metabolic/cardiovascular markers in IUGR children.
Main Methods:
- Plasma cortisol (F) and cortisone (E) concentrations, and the F/E ratio, were measured in 40 IUGR children without catch-up growth and 26 controls.
- Cholesterol, HbA1C, insulin, and glucose levels were also determined.
- Children were categorized into two groups based on their F/E ratios: Group 1 (high F/E ratio) and Group 2 (normal F/E ratio).
Main Results:
- Twenty percent of IUGR children (Group 1) exhibited significantly higher F/E ratios (13.15 +/- 4.26) compared to controls (5.5 +/- 1.7) and Group 2 (5.40 +/- 1.43).
- Group 1 children had significantly lower childhood height, higher systolic blood pressure, and higher cholesterol concentrations compared to Group 2 and controls.
- Height was negatively correlated with the F/E ratio, and cholesterol levels were positively correlated with the F/E ratio.
Conclusions:
- A subset of children with IUGR and poor growth demonstrates elevated F/E ratios, indicative of a possible partial 11beta-HSD2 deficit.
- This finding suggests a potential link between 11beta-HSD2 function during fetal development and long-term health outcomes, including cardiovascular risk.
- Further evaluation is needed to determine if these children face an increased risk of developing cardiovascular diseases in adulthood.
Abstract:
We evaluated the involvement of a possible dysfunction of 11beta-hydroxysteroid dehydrogenase type 2 (11beta-HSD2) in the fetal growth retardation and poor growth rates of children born with intrauterine growth retardation (IUGR). Children with IUGR have a nephron deficit and are also at risk of developing cardiovascular diseases, high blood pressure, glucose intolerance, and dyslipidemia later in life. The major site of 11beta-HSD2 production is the kidney and its deficit causes hypertension. We investigated plasma concentrations of cortisol (F) and cortisone (E) and the F/E ratio in 26 control children and in 40 IUGR children without catch-up growth. We also determined cholesterol, HbA1C, insulin, and glucose levels in plasma. Mean F values were 106 +/- 54.2 ng/mL in control children and 114.6 +/- 53.2 ng/mL in IUGR children. Mean E values were 19.5 +/- 7.1 ng/mL in control children and 17.9 +/- 6.85 ng/mL in IUGR children. The mean F/E ratio for control children was 5.5 +/- 1.7. Eight (20%) of the IUGR children (IUGR children of group 1) had high F/E ratios more than 2 SD above the normal mean: 13.15 +/- 4.26, (p < 0.0001) as compared to control children, whereas the other 32 children (IUGR children of group 2) had normal F/E ratios: 5.40 +/- 1.43 (p = 0.68). Childhood height was significantly lower for group 1 than group 2 children (-3.63 SD and -2.92 SD, respectively: p < 0.01) and was negatively correlated with the F/E ratio (p < 0.01). Systolic blood pressure was higher for group 1 (p = 0.005) and for group 2 (p = 0.015) than for control children. The diastolic pressure in IUGR children of group 1 was higher than that in control children (p = 0.013) and slightly higher than that in group 2 (p = 0.1, ns). Cholesterol concentrations were higher in group 1 than in group 2 (p = 0.029), and controls (p = 0.017) and correlated positively with F/E (0.02 < p < 0.05). Fasting insulin concentrations were higher in group 1 than in group 2 (ns) and controls (ns). There was no difference in mean fasting glucose concentrations, or HbA1C between the three groups. Twenty percent of our children with IUGR and poor growth rates had high F/E ratios, suggesting a possible partial 11beta-HSD2 deficit. Whether these children are at high risk of developing cardiovascular diseases as adults remains to be further evaluated.
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