Literature DB >> 29176461

Impact of Hydroxyurea on Anthropometry and Serum 25-Hydroxyvitamin D Among Children With Sickle Cell Disease.

Samuel A Adegoke1,2, Josefina A P Braga3, Adekunle D Adekile4, Maria S Figueiredo1.   

Abstract

OBJECTIVE: To evaluate the impact of hydroxyurea (HU) on nutritional status and serum 25-hydroxyvitamin D (25-OHD) of children with sickle cell disease (SCD).
DESIGN: Anthropometry and serum 25-OHD were determined in 98 children with SCD, comprising of 68 in HU-group and 30 in HU-naive group.
RESULTS: Underweight was more common among HU-naive group (33.3% vs. 10.3%, P=0.009), while 79.4% of HU-group against 56.7% HU-naive had normal body mass index percentile for age and sex, P=0.028. None of the HU-group compared with 13.3% of the HU-naive had severe vitamin D deficiency, P=0.002. The mean 25-OHD of the HU-group was also higher (24.1±1.2 vs. 19.1±9.8 ng/mL, P=0.007).
CONCLUSIONS: HU possibly ameliorate growth retardation and vitamin D deficiency in children with SCD.

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Year:  2018        PMID: 29176461     DOI: 10.1097/MPH.0000000000001002

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  2 in total

1.  Height-corrected low bone density associates with severe outcomes in sickle cell disease: SCCRIP cohort study results.

Authors:  Oyebimpe O Adesina; James G Gurney; Guolian Kang; Martha Villavicencio; Jason R Hodges; Wassim Chemaitilly; Sue C Kaste; Babette S Zemel; Jane S Hankins
Journal:  Blood Adv       Date:  2019-05-14

2.  Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease.

Authors:  Anna M Hood; Charles T Quinn; Christopher D King; Lisa M Shook; James L Peugh; Lori E Crosby
Journal:  Complement Ther Med       Date:  2020-02-15       Impact factor: 2.446

  2 in total

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