Prevention of bone loss in children receiving long-term glucocorticoids with calcium and alfacalcidol or menatetrenone.
Study Goal
The researchers aimed to compare the efficacy of alfacalcidol and menatetrenone, both supplemented with calcium, in preventing bone loss in children on long-term glucocorticoid treatment.
Results Summary
Both treatments increased bone mineral content (BMC) and bone mineral density (BMD), but alfacalcidol showed superior results in preventing bone loss, particularly in bone mineral apparent density (BMAD), compared to menatetrenone.
Population
Children on stable long-term glucocorticoid treatment.
Effective Dosage
400 mg of elemental calcium daily.
Duration
12 months.
Interactions
None mentioned.
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
alfacalcidol | increase | BMC and BMD | children treated with long-term glucocorticoids | - | significantly increased | #1 |
menatetrenone | increase | BMC and BMD | children treated with long-term glucocorticoids | - | significantly increased | #2 |
menatetrenone | decrease | BMD Z-score | children treated with long-term glucocorticoids | - | significantly decreased | #3 |
alfacalcidol | increase | BMAD | children treated with long-term glucocorticoids | - | significantly increased | #4 |
Calcium supplementation along with alfacalcidol | decrease | bone loss | children treated with long-term glucocorticoids | - | can prevent further bone loss to a greater extent than menatetrenone | #5 |
BACKGROUND: Long-term treatment with glucocorticoids can induce bone loss and increase fracture risks. AIM: To compare the efficacy of a 12-month treatment between alfacalcidol and menatetrenone in preventing bone loss in children treated with long-term glucocorticoids. PATIENTS AND METHODS: Twenty children on a stable dosage of glucocorticoids were randomly divided into two groups (alfacalcidol or menatetrenone). Each group received the assigned treatment along with 400 mg of elemental calcium daily for 12 months. Patients receiving medications affecting bone metabolism or patients with impaired kidney function were excluded. Bone density parameters, including lumbar spine bone mineral content (BMC), bone mineral density (BMD), and BMD Z-score were assessed by dual-energy X-ray absorptiometry at baseline and at 12-month follow-up. Bone mineral apparent density (BMAD) was calculated as a size-adjusted measurement of BMD in growing children. Baseline characteristics and bone density parameters were similar between both groups. RESULTS: After 12 months, BMC and BMD were significantly increased from baseline in both groups, but did not differ between the groups. The BMD Z-score at 12-month follow-up was significantly decreased from baseline in the menatetrenone group. BMAD was significantly increased from baseline in the alfacalcidol group. CONCLUSIONS: Administration of long-term glucocorticoids in children justifies an intervention to preserve bone mass. Calcium supplementation along with alfacalcidol can prevent further bone loss to a greater extent than menatetrenone in this group of patients.