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Published on: January 7, 2016
Adiponectin levels in prepubertal children with Prader-Willi syndrome before and during growth hormone therapy
D A M Festen1, A van Toorenenbergen, H J Duivenvoorden
1Dutch Growth Foundation, Westzeedijk 106, 3016 AH Rotterdam, The Netherlands. d.festen@erasmusmc.nl
Insights
Children with Prader-Willi syndrome (PWS) have higher adiponectin and body fat levels. Growth hormone (GH) treatment increased adiponectin, suggesting it may help manage metabolic health in PWS patients.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Genetics
Background:
- Prader-Willi syndrome (PWS) is associated with obesity and abnormal body composition, including high body fat percentage, even in normal-weight children.
- Adiponectin, a hormone, is known to have an inverse relationship with obesity and insulin resistance.
Purpose of the Study:
- Evaluate adiponectin levels, body composition, carbohydrate metabolism, and triglycerides in prepubertal children with PWS.
- Examine the associations between adiponectin and these metabolic markers.
- Assess the effects of growth hormone (GH) treatment on these outcomes in PWS children.
Main Methods:
- A study involving twenty prepubertal children diagnosed with Prader-Willi syndrome.
- Participants were randomized into two groups: one receiving GH treatment (1 mg/m2.d) and a control group without GH treatment.
- Fasting levels of adiponectin, glucose, insulin, and triglycerides were measured at baseline and after 1 and 2 years. Body composition was assessed using dual-energy x-ray absorptiometry.
Main Results:
- PWS children exhibited significantly higher adiponectin levels compared to healthy controls.
- A significant elevation in body fat percentage was observed in PWS children.
- Adiponectin levels showed an inverse correlation with triglyceride levels and a tendency towards inverse relationships with body fat percentage and BMI, but not with glucose or insulin metabolism markers.
- GH treatment led to a significant increase in adiponectin levels, while levels remained unchanged in the control group.
Conclusions:
- Prepubertal children with PWS have elevated adiponectin levels, inversely associated with triglycerides, despite a high body fat percentage.
- Growth hormone treatment further increased adiponectin levels in PWS children, offering reassurance regarding the development of insulin resistance.
- These findings highlight the complex metabolic profile in PWS and the potential role of GH in modulating adiponectin and related metabolic parameters.
Context:
Children with Prader-Willi syndrome (PWS) may have obesity and an abnormal body composition with a high body fat percentage, even if they have a normal body weight. Adiponectin has been inversely related to obesity and insulin resistance.
Objective:
The objective of the study was to evaluate in prepubertal PWS children the following: 1) adiponectin levels, body composition, carbohydrate metabolism, and triglyceride levels; 2) associations between adiponectin and body composition, carbohydrate metabolism, and triglycerides; and 3) effects of GH treatment on these outcome measures.
Patients:
Twenty prepubertal PWS children participated in the study.
Intervention:
The subjects were randomized into a GH treatment group (n=10, 1 mg/m2.d) and a non-GH-treated control group (n=10).
Main Outcome Measures:
At baseline, after 1 and 2 yr of GH treatment, fasting levels of adiponectin, glucose, insulin, and triglycerides were assessed. Body composition and fat distribution were measured by dual energy x-ray absorptiometry.
Results:
PWS children had significantly higher median (interquartile range) adiponectin levels [17.1 mg/liter (13.9-23.2)] than healthy sex- and age-matched controls [11.8 mg/liter (9.7-12.5), P<0.005]. Body fat percentage was significantly higher than 0 sd score [1.8 sd score (1.5-2.1), P<0.001]. Adiponectin levels were inversely related to triglyceride levels (r=-0.52, P=0.03). There was a tendency to an inverse relation with body fat percentage and body mass index, but no correlation with fasting insulin or glucose levels, the insulin to glucose ratio, or homeostasis model assessment index. During GH treatment, adiponectin levels increased significantly and did not change in randomized controls.
Conclusion:
Adiponectin levels were increased, and inversely associated with triglyceride levels, in prepubertal, not overweight PWS children, although they had a relatively high body fat percentage. During GH treatment, adiponectin levels further increased, whereas no change was found in the controls, which is reassuring with respect to the development of insulin resistance during GH treatment.
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