Leptin may play a role in bone microstructural alterations in obese children
P Dimitri1, R M Jacques, M Paggiosi
1Department of Paediatric Endocrinology (P.D., D.K.), Sheffield Children's NHS Foundation Trust, Sheffield, S10 2TH, United Kingdom; School of Health and Related Research (R.M.J.), The Mellanby Centre for Bone Research (M.P., J.W., N.B., R.E.), Academic Unit of Bone Metabolism, and Centre for Computational Imaging and Simulation Technologies in Biomedicine, Department of Mechanical Engineering (Z.A.T., A.F.F.), University of Sheffield, Sheffield, S10 2TN, United Kingdom.
Childhood obesity alters bone structure, with higher leptin levels potentially driving these changes. However, obese children
Area of Science:
- Pediatric Endocrinology
- Bone Biology
- Obesity Research
Background:
- Obesity in children is linked to lower bone mass and higher fracture risk.
- The impact of hormonal changes on skeletal microstructure and biomechanics in obese children remains understudied.
Purpose of the Study:
- To investigate the relationship between obesity-associated hormonal alterations and skeletal microstructure and biomechanics in children.
- To determine how hormones like leptin, adiponectin, and sex hormones correlate with bone health indicators.
Main Methods:
- High-resolution peripheral quantitative computed tomography (HR-pQCT) was employed to assess bone microstructure and biomechanics in obese and lean children.
- Participants were matched for gender and pubertal stage.
- Hormonal levels (leptin, adiponectin, testosterone, estrogen, osteocalcin, sclerostin) were analyzed in relation to skeletal parameters.
Main Results:
- Obese children exhibited lower radial cortical porosity and pore diameter, and lower tibial trabecular thickness but higher trabecular number.
- Higher fat mass percentage correlated with reduced cortical porosity and trabecular thickness.
- Elevated leptin levels in obese children were inversely associated with radial cortical porosity and tibial trabecular thickness.
Conclusions:
- Childhood obesity significantly alters radial and tibial bone microstructure, with leptin potentially mediating these effects.
- Despite microstructural changes, the biomechanical properties of the radius and tibia in obese children do not adequately compensate for increased loading.
- These findings suggest a potential mechanism explaining the elevated fracture risk observed in obese children.
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