Literature DB >> 15238915

Vitamin A status, hospitalizations, and other outcomes in young children with sickle cell disease.

Joan I Schall1, Babette S Zemel, Deborah A Kawchak, Kwaku Ohene-Frempong, Virginia A Stallings.   

Abstract

OBJECTIVE: To determine the relation of serum vitamin A status to growth, nutritional and hematologic status, and to the number of hospitalizations in children with sickle cell disease-SS (homozygous for the S allele, SCD-SS). STUDY
DESIGN: Children (2-9.9 years of age) with SCD-SS were assessed for serum retinol, hemoglobin, hematocrit, reticulocyte count, height, weight, body mass index, and recalled dietary intake. Vitamin A status was defined on the basis of serum retinol concentration as suboptimal (<30 microg/dL) and normal (> or =30 microg/dL). Hospitalizations were determined for 1 year after vitamin A assessment.
RESULTS: Mean serum retinol was 26.7 +/- 6.8 microg/dL in 66 subjects (39 girls) and was suboptimal in 66% of children. Compared with those with normal status, children with suboptimal vitamin A had significantly lower body mass index z score (-0.7 +/- 1.0 vs -0.1 +/- 0.6) and hemoglobin (7.9 +/- 1.1 vs 8.5 +/- 1.1), and hematocrit (23.3 +/- 3.0 vs 25.1 +/- 3.8) and significantly more hospitalizations (2.8 +/- 2.0 vs 0.7 +/- 0.8). After adjusting for age and sex, suboptimal vitamin A status was associated with a 10-fold increased risk for hospitalization (OR, 10.5; 95% CI, 2.3, 48.6) and with increased pain (OR,5.3; 95% CI, 1.3, 21.6) and fever episodes (OR, 6.4; 95% CI, 1.7, 24.9) requiring hospitalization.
CONCLUSIONS: Suboptimal vitamin A status was prevalent in US children with SCD-SS and was associated with increased hospitalizations and poor growth and hematologic status.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15238915     DOI: 10.1016/j.jpeds.2004.03.051

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  15 in total

1.  Attenuated maximal muscle strength and peak power in children with sickle cell disease.

Authors:  Kelly A Dougherty; Joan I Schall; Alisha J Rovner; Virginia A Stallings; Babette S Zemel
Journal:  J Pediatr Hematol Oncol       Date:  2011-03       Impact factor: 1.289

2.  Malnutrition in Sickle Cell Anemia: Implications for Infection, Growth, and Maturation.

Authors:  Hyacinth I Hyacinth; Oluwatoyosi A Adekeye; Christopher S Yilgwan
Journal:  J Soc Behav Health Sci       Date:  2013-01-01

3.  Food insecurity, housing instability, and dietary quality among children with sickle cell disease: Assessment from a single urban center.

Authors:  Cristina R Fernández; Maureen Licursi; Randi Wolf; Margaret T Lee; Nancy S Green
Journal:  Pediatr Blood Cancer       Date:  2021-11-22       Impact factor: 3.167

Review 4.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

5.  Hemoglobin alters vitamin carrier uptake and vitamin D metabolism in proximal tubule cells: implications for sickle cell disease.

Authors:  Megan L Gliozzi; Youssef Rbaibi; Kimberly R Long; Dario A Vitturi; Ora A Weisz
Journal:  Am J Physiol Cell Physiol       Date:  2019-09-11       Impact factor: 4.249

6.  Nutritional deficiencies in iron overloaded patients with hemoglobinopathies.

Authors:  Susan Claster; John C Wood; Leila Noetzli; Susan M Carson; Thomas C Hofstra; Rachna Khanna; Thomas D Coates
Journal:  Am J Hematol       Date:  2009-06       Impact factor: 10.047

7.  No improvement in suboptimal vitamin A status with a randomized, double-blind, placebo-controlled trial of vitamin A supplementation in children with sickle cell disease.

Authors:  Kelly A Dougherty; Joan I Schall; Deborah A Kawchak; Michael H Green; Kwaku Ohene-Frempong; Babette S Zemel; Virginia A Stallings
Journal:  Am J Clin Nutr       Date:  2012-09-05       Impact factor: 7.045

8.  Clinical Observations, Plasma Retinol Concentrations, and In Vitro Lymphocyte Functions in Children With Sickle Cell Disease.

Authors:  Solo R Kuvibidila; Renée Gardner; Maria Velez; Raj Warrier
Journal:  Ochsner J       Date:  2018

Review 9.  Growth and Growth hormone - Insulin Like Growth Factor -I (GH-IGF-I) Axis in Chronic Anemias.

Authors:  Ashraf T Soliman; Vincenzo De Sanctis; Mohamed Yassin; Ashraf Adel
Journal:  Acta Biomed       Date:  2017-04-28

10.  Effects of nutritional intake on disease severity in children with sickle cell disease.

Authors:  Valentina Mandese; Francesca Marotti; Luca Bedetti; Elena Bigi; Giovanni Palazzi; Lorenzo Iughetti
Journal:  Nutr J       Date:  2016-04-30       Impact factor: 3.271

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.