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Randomized Controlled Trial
. 2020 Sep-Oct;34(5):424-434.
doi: 10.1016/j.pedhc.2020.04.007. Epub 2020 Jun 5.

Vitamin D Supplementation Improves Health-Related Quality of Life and Physical Performance in Children with Sickle Cell Disease and in Healthy Children

Randomized Controlled Trial

Vitamin D Supplementation Improves Health-Related Quality of Life and Physical Performance in Children with Sickle Cell Disease and in Healthy Children

Kelly A Dougherty et al. J Pediatr Health Care. 2020 Sep-Oct.

Abstract

Introduction: No study determined if vitamin D supplementation improves health-related quality of life (HRQL) using pediatric Patient-Reported Outcomes Measurement Information System or physical functioning in type SS sickle cell disease (HbSS).

Method: Subjects with HbSS (n = 21) and healthy subjects (n = 23) were randomized to daily oral doses (4,000 vs. 7,000 IU) of cholecalciferol (vitamin D3) and evaluated at 6 and 12 weeks for changes in serum 25 hydroxyvitamin D (25(OH)D), HRQL, and physical functioning.

Results: In subjects with HbSS, significant reductions in pain, fatigue, and depressive symptoms and improved upper-extremity function were observed. In healthy subjects, significant reductions in fatigue and improved upper-extremity function were observed. Significant improvements in peak power and dorsiflexion isometric maximal voluntary contraction torques were observed in both groups. In subjects with HbSS, improved plantar flexion isometric maximal voluntary contraction torques were observed. Both groups saw significant improvement in their total Bruininks-Oseretsky Test of Motor Proficiency score.

Discussion: Daily high-dose vitamin D supplementation for African American children with and without HbSS improved HRQL and physical performance.

Keywords: Sickle cell disease; muscle strength; physical performance; quality of life; vitamin D supplementation.

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Conflict of interest statement

Declaration of Conflicting Interests

The authors declare that there is no conflict of interest.

References

    1. Adegoke SA, Oyelami OA, Adekile A, & Figueiredo MS (2017). Influence of serum 25-hydroxyvitamin D on the rate of pain episodes in Nigerian children with sickle cell anaemia. Paediatr Int Child Health, 37(3), 217–221. doi:10.1080/20469047.2017.1295012 - DOI - PubMed
    1. Ameringer S, Elswick RK Jr., & Smith W. (2014). Fatigue in adolescents and young adults with sickle cell disease: biological and behavioral correlates and health-related quality of life. Journal of Pediatric Oncology Nursing, 31(1), 6–17. doi:10.1177/1043454213514632 - DOI - PMC - PubMed
    1. Anderson LM, Allen TM, Thornburg CD, & Bonner MJ (2015). Fatigue in Children With Sickle Cell Disease: Association With Neurocognitive and Social-Emotional Functioning and Quality of Life. Journal of Pediatric Hematology/Oncology, 37(8), 584–589. doi:10.1097/mph.0000000000000431 - DOI - PubMed
    1. Bakshi N, Lukombo I, Belfer I, & Krishnamurti L. (2018). Pain catastrophizing is associated with poorer health-related quality of life in pediatric patients with sickle cell disease. Journal of Pain Research, 11, 947–953. doi:10.2147/jpr.s151198 - DOI - PMC - PubMed
    1. Bakshi N, Ross D, & Krishnamurti L. (2018). Presence of pain on three or more days of the week is associated with worse patient reported outcomes in adults with sickle cell disease. Journal of Pain Research, 11, 313–318. doi:10.2147/jpr.s150065 - DOI - PMC - PubMed

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