Literature DB >> 1550264

Nutritional status and dietary intake of children with sickle cell anemia.

N T Gray1, J M Bartlett, K M Kolasa, S P Marcuard, C T Holbrook, R D Horner.   

Abstract

The nutritional status and dietary intake of children with sickle cell anemia were examined to confirm the presence of deficiencies. Nine children with sickle cell anemia and 19 controls were assessed. Resting energy expenditure was measured with open circuit indirect calorimetry and body composition was estimated from skinfold measurements. Three-day food records were analyzed for protein, zinc, vitamin A, folic acid, and iron content. Serum vitamin A, red blood cell zinc, red blood cell folate, serum folate, serum ferritin, hematocrit, total urine nitrogen, and 24-h urine creatinine levels were measured. The children with sickle cell anemia were leaner, weighed less, and had lower red blood cell zinc levels, lower serum vitamin A levels, lower urine nitrogen levels, and greater resting energy expenditure than controls. Serum and red blood cell folate levels were within normal ranges and similar to controls. The serum ferritin level was higher than controls and higher than normal for age. Dietary intake of energy and protein was more than that of controls, and dietary intake of zinc, vitamin A, folic acid, and iron was similar to that of controls and adequate compared to the Recommended Dietary Allowances. Further studies are needed to explain the physical and biochemical differences seen in children with sickle cell anemia despite dietary intakes that appear to be adequate and similar to those of controls.

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Year:  1992        PMID: 1550264     DOI: 10.1097/00043426-199221000-00008

Source DB:  PubMed          Journal:  Am J Pediatr Hematol Oncol        ISSN: 0192-8562


  14 in total

1.  Tumor necrosis factor alpha in children with sickle cell disease in stable condition.

Authors:  S Kuvibidila; R Gardner; D Ode; L Yu; G Lane; R P Warrier
Journal:  J Natl Med Assoc       Date:  1997-09       Impact factor: 1.798

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.  The relationship of oxygen transport and cardiac index for the prevention of sickle cell crises.

Authors:  Kevin Farrell; Leon Dent; Minh Ly Nguyen; Maciej Buchowski; Ananta Bhatt; Maria del Pilar Aguinaga
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

4.  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

5.  TNF-α, IFN-γ, IL-10, and IL-4 levels were elevated in a murine model of human sickle cell anemia maintained on a high protein/calorie diet.

Authors:  Hyacinth I Hyacinth; Patrice L Capers; David R Archer; Jacqueline M Hibbert
Journal:  Exp Biol Med (Maywood)       Date:  2013-11-26

6.  The Role of Nutrition in Sickle Cell Disease.

Authors:  H I Hyacinth; B E Gee; J M Hibbert
Journal:  Nutr Metab Insights       Date:  2010-01-01

7.  Nutritional status of young children with inherited blood disorders in western Kenya.

Authors:  Becky L Tsang; Kevin M Sullivan; Laird J Ruth; Thomas N Williams; Parminder S Suchdev
Journal:  Am J Trop Med Hyg       Date:  2014-03-17       Impact factor: 2.345

Review 8.  Prevalence of vitamin D deficiency in sickle cell disease: a systematic review.

Authors:  Vikki G Nolan; Kerri A Nottage; Elliott W Cole; Jane S Hankins; James G Gurney
Journal:  PLoS One       Date:  2015-03-03       Impact factor: 3.240

Review 9.  Phytomedicines and nutraceuticals: alternative therapeutics for sickle cell anemia.

Authors:  Ngozi Awa Imaga
Journal:  ScientificWorldJournal       Date:  2013-02-14

10.  Prevalence of Vitamin D Deficiency Varies Widely by Season in Canadian Children and Adolescents with Sickle Cell Disease.

Authors:  Kaitlyn L I Samson; Heather McCartney; Suzanne M Vercauteren; John K Wu; Crystal D Karakochuk
Journal:  J Clin Med       Date:  2018-01-30       Impact factor: 4.241

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