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Association Between Secondary Hyperparathyroidism and Body Composition in Pediatric Patients With Moderate and
Vasiliki Karava1, Antonia Kondou1, John Dotis1
1Pediatric Nephrology Unit, First Department of Pediatrics, Hippokratio General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Insights
Secondary hyperparathyroidism links to high adiposity in moderate chronic kidney disease (CKD) but not advanced CKD, with leptin potentially involved. In advanced CKD, higher alfacalcidol doses may prevent muscle wasting.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Metabolic Bone Disease
Background:
- Secondary hyperparathyroidism is common in pediatric chronic kidney disease (CKD).
- Body composition changes, including muscle wasting and adiposity, are prevalent in pediatric CKD.
- The relationship between secondary hyperparathyroidism and body composition in pediatric CKD requires further investigation.
Purpose of the Study:
- To investigate the association between secondary hyperparathyroidism and body composition in pediatric patients with moderate (stage 3) and advanced (stage 4-5) CKD.
- To explore the role of serum leptin and alfacalcidol index in these associations.
Main Methods:
- Cross-sectional study of 61 pediatric patients with moderate to advanced CKD.
- Body composition assessed using multi-frequency bio-impedance spectroscopy (lean tissue index, fat tissue index).
- Serum intact parathormone (iPTH), calcium, phosphorus, 25-hydroxyvitamin D, and leptin levels measured; alfacalcidol index calculated for advanced CKD.
Main Results:
- In moderate CKD, high iPTH correlated with higher fat tissue index and lower lean tissue index, and was associated with high adiposity, potentially mediated by leptin.
- In advanced CKD, no significant correlation was found between iPTH and body composition or leptin.
- In advanced CKD, muscle wasting was associated with a lower alfacalcidol index, suggesting a potential benefit of higher alfacalcidol dosing.
Conclusions:
- Secondary hyperparathyroidism is linked to high adiposity in moderate pediatric CKD, with leptin as a possible factor.
- In advanced pediatric CKD, the relationship between secondary hyperparathyroidism and body composition differs, and alfacalcidol dosing may be crucial for preventing muscle wasting.
Abstract:
Objective: This single center cross-sectional study aims to investigate the association between secondary hyperparathyroidism and body composition in pediatric patients with moderate (stage 3) and advanced (stage 4-5) chronic kidney disease (CKD). Methods: 61 patients (median age: 13.4 years) were included. Body composition indices, including lean tissue index (LTI) and fat tissue index (FTI), were measured using multi-frequency bio-impedance spectroscopy. Muscle wasting was defined as LTI adjusted to height-age (HA) z-score < -1.65 SD and high adiposity as FTI z-score > 1.65 SD. Serum mineral metabolism parameters, including serum intact parathormone (iPTH), calcium, phosphorus and 25-hydroxyvitamin D, as well as serum leptin were measured in each patient. In advanced CKD patients, the mean values of serum mineral laboratory parameters of the 6 months prior to body composition assessment were recorded, and alfacalcidol index, defined as weekly alfacalcidol dose (mcg/week) per pg/ml of iPTH × 1,000, was calculated. Results: In moderate CKD (31 patients), high iPTH (>90 ng/ml) was observed in 10 (32.3%) patients and was associated with higher FTI z-score (p = 0.022). Moreover, serum iPTH was negatively correlated to LTI HA z-score (rs = -0.486, p = 0.006), and positively correlated to serum leptin levels (rs = 0.369, p = 0.041). The positive correlation between FTI z-score and iPTH (rs = 0.393, p = 0.039) lost significance after adjustment for serum leptin. iPTH was positively associated with high adiposity (12 patients, 38.7%) after adjustment for the other mineral metabolism parameters (OR 1.023, 95% CI 1.002-1.045, p = 0.028). In advanced CKD (30 patients), no significant correlation was observed between iPTH and body composition indices and serum leptin levels. Eleven (36.7%) patients with muscle wasting presented lower alfacalcidol index (p = 0.017). Alfacalcidol index ≤ 24 was strongly associated with muscle wasting after adjustment for CKD stage and other mineral metabolism parameters (OR 7.226, 95% CI 1.150-45.384, p = 0.035). Conclusion: Secondary hyperparathyroidism is associated with high adiposity in moderate but not in advanced CKD, with leptin acting as a potential contributive factor. In advanced CKD, targeting higher alfacalcidol weekly dose per each unit of serum PTH seems beneficial for preventing muscle wasting.
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