Safety and efficacy of monthly high-dose vitamin D3 supplementation in children and adolescents with sickle cell disease

被引:0
|
作者
Hanna, Diana [1 ]
Kamal, Doaa E. [2 ]
Fawzy, Hebatallah M. [3 ]
Elkhalek, Reham Abd [2 ]
机构
[1] Zagazig Univ, Fac Med, Pediat Dept, Pediat Hematol & Oncol Unit, Zagazig, Egypt
[2] Zagazig Univ, Fac Med, Rheumatol & Rehabil Dept, Zagazig, Egypt
[3] Zagazig Univ, Fac Med, Publ Hlth & Community Med Dept, Zagazig, Egypt
关键词
Vitamin D supplementation; Sickle cell disease (SCD); Hand grip strength (HGS); Health-related quality of life (HRQL); QUALITY-OF-LIFE; HEALTH-ASSESSMENT QUESTIONNAIRE; D DEFICIENCY; YOUNG-ADULTS; PAIN; FATIGUE;
D O I
10.1007/s00431-024-05572-w
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Little is known about the impact of vitamin D supplementation on hand grip strength (HGS) and health-related quality of life (HRQoL) in children and adolescents with sickle cell disease (SCD). We aimed to evaluate the safety and efficacy of monthly high-dose vitamin D3 supplementation and its implications on bone mineral density (BMD), HGS, and HRQoL in patients with SCD and healthy controls. The study included 42 children with SCD and 42 healthy matched controls. The study participants were supplemented with high-dose monthly oral vitamin D3. Changes in the serum level of 25(OH) vitamin D3, maximum HGS, and BMD from baseline to 6 months were assessed, and the HRQoL questionnaire and Childhood Health Assessment Questionnaire (CHAQ) were used to evaluate the functional capacity. At baseline, SCD subjects had poorer growth status indicated by negative Z scores. Suboptimal BMD was detected by significantly lower Z score, and lower HGS and worse HRQL parameters were found compared to the controls (P < 0.001). Median 25(OH) vitamin D3 was significantly lower in SCD patients compared to controls (16.5 vs. 28 ng/mL, respectively (P < 0.001)). After 6 months of vitamin D supplementation, there was significant improvement in the DEXA Z-score (P < 0.001), limitation of physical health (P = 0.02), pain scores (P < 0.001), and CHAQ grades (P = 0.01) in SCD patients. A significant improvement in HGS (P < 0.001 and P = 0.005) as well as the CHAQ score (P < 0.001 and P = 0.003) was detected in the SCD group and controls, respectively. There were no reported clinical adverse events (AEs) or new concomitant medications (CMs) during the study duration, and safe levels of Ca and 25 (OH) D3 were observed at 3 and 6 months for both groups. There was a significant positive correlation between HGS and total physical score (r = 0.831, P < 0.001) and a negative correlation with CHAQ score (r = - 0.685, P < 0.001). We also detected a significant positive correlation between vitamin D levels at 6 months and HGS (r = 0.584, P < 0.001), pain score (r = 0.446, P < 0.001), and a negative correlation with CHAQ score (r = - 0.399, P < 0.001). Conclusion: Monthly oral high-dose vitamin D supplementation was safe and effective in improving vitamin D levels, HGS, and HRQoL in SCD children and healthy subjects, and BMD scores in SCD patients. Further randomized controlled trials are warranted to assess an optimal dosing strategy and to investigate the impact on clinically significant outcomes in children and adolescents with SCD and their healthy counterparts.
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页码:3347 / 3357
页数:11
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