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

被引:9
作者
Adegoke, Samuel A. [1 ,3 ]
Braga, Josefina A. P. [2 ]
Adekile, Adekunle D. [4 ]
Figueiredo, Maria S. [1 ]
机构
[1] Univ Fed Sao Paulo, Haematol & Blood Transfus Div, Sao Paulo, Brazil
[2] Univ Fed Sao Paulo, Dept Pediat, Escola Paulista Med, Sao Paulo, Brazil
[3] Obafemi Awolowo Univ, Dept Pediat & Child Hlth, PMB 013, Ife, Nigeria
[4] Kuwait Univ, Dept Paediat, Fac Med, Kuwait, Kuwait
关键词
fat percentage; growth; hydroxyurea; 25-hydroxyvitamin D; nutritional status; VITAMIN-D DEFICIENCY; GROWTH; ANEMIA;
D O I
10.1097/MPH.0000000000001002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 (24.11.2 vs. 19.1 +/- 9.8ng/mL, P=0.007). Conclusions: HU possibly ameliorate growth retardation and vitamin D deficiency in children with SCD.
引用
收藏
页码:E243 / E247
页数:5
相关论文
共 23 条
  • [1] Definitions of the phenotypic manifestations of sickle cell disease
    Ballas, Samir K.
    Lieff, Susan
    Benjamin, Lennette J.
    Dampier, Carlton D.
    Heeney, Matthew M.
    Hoppe, Carolyn
    Johnson, Cage S.
    Rogers, Zora R.
    Smith-Whitley, Kim
    Wang, Winfred C.
    Telen, Marilyn J.
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 2010, 85 (01) : 6 - 13
  • [2] Bandeira Francisco, 2006, Arq Bras Endocrinol Metab, V50, P640, DOI 10.1590/S0004-27302006000400009
  • [3] Total and resting energy expenditure in children with sickle cell disease
    Barden, EM
    Zemel, BS
    Kawchak, DA
    Goran, MI
    Ohene-Frempong, K
    Stallings, VA
    [J]. JOURNAL OF PEDIATRICS, 2000, 136 (01) : 73 - 79
  • [4] Braga JAP, 1995, ARCH LATINOAM NUTR, V45, P198
  • [5] Weight Status of Children With Sickle Cell Disease
    Chawla, Anjulika
    Sprinz, Philippa G.
    Welch, Jennifer
    Heeney, Matthew
    Usmani, Naheed
    Pashankar, Farzana
    Kavanagh, Patricia
    [J]. PEDIATRICS, 2013, 131 (04) : E1168 - E1173
  • [6] Frisancho A.R., 1990, Antropometric standards for the assessment of growth and nutritional status
  • [7] GRUNBERG J, 1981, COURRIER, V31, P492
  • [8] Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study
    Hankins, JS
    Ware, RE
    Rogers, ZR
    Wynn, LW
    Lane, PA
    Scott, JP
    Wang, WC
    [J]. BLOOD, 2005, 106 (07) : 2269 - 2275
  • [9] Vitamin D Deficiency and Acute Vaso-occlusive Complications in Children With Sickle Cell Disease
    Lee, Margaret T.
    Licursi, Maureen
    McMahon, Donald J.
    [J]. PEDIATRIC BLOOD & CANCER, 2015, 62 (04) : 643 - 647
  • [10] GROWTH STATUS IN CHILDREN AND ADOLESCENTS WITH SICKLE CELL DISEASE
    Mitchell, Monica J.
    Carpenter, Gloria J. O.
    Crosby, Lori E.
    Bishop, Chanelle T.
    Hines, Janelle
    Noll, Jennie
    [J]. PEDIATRIC HEMATOLOGY AND ONCOLOGY, 2009, 26 (04) : 202 - 215