Literature DB >> 2858749

Growth retardation in sickle-cell disease treated by nutritional support.

M B Heyman, E Vichinsky, R Katz, B Gaffield, D Hurst, R Castillo, D Chiu, K Kleman, A J Ammann, M M Thaler.   

Abstract

The effect of increased nutritional intake was evaluated in 5 growth-retarded children with sickle-cell disease. Growth on recommended daily calorie and protein intakes had been inadequate in all 5. Fat absorption and intestinal mucosal morphology were normal in all 5. 2 children were given nutritional supplementation by nasogastric intubation, 1 received nightly oral formula supplements, and 2 were supplemented with zinc, iron, folate, and vitamin E only. Nutritional supplementation by the nasogastric route produced a rapid sustained increase in growth rate, associated with striking reductions in pain crises and infections which had previously necessitated many hospital admissions. Oral supplementation improved the clinical course but had no effect on growth rate. Mineral and vitamin supplements influenced neither the growth rate nor the clinical course. The observations indicate that nasogastric nutritional supplementation may accelerate growth and reduce the incidence and severity of complications in growth-retarded children with sickle-cell disease.

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Year:  1985        PMID: 2858749     DOI: 10.1016/s0140-6736(85)91677-0

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  17 in total

1.  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

2.  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

3.  Nutritional supplement profile of adults with sickle cell disease.

Authors:  Elena M Crouch; Vence L Bonham; Khadijah Abdallah; Ashley Buscetta; Giacomo Vinces; Moonseong Heo; Caterina P Minniti
Journal:  Am J Hematol       Date:  2018-05-04       Impact factor: 10.047

4.  C-reactive protein and interleukin-6 are decreased in transgenic sickle cell mice fed a high protein diet.

Authors:  David R Archer; Jonathan K Stiles; Gale W Newman; Alexander Quarshie; Lewis L Hsu; Phouyong Sayavongsa; Jennifer Perry; Elizabeth M Jackson; Jacqueline M Hibbert
Journal:  J Nutr       Date:  2008-06       Impact factor: 4.798

5.  Transport proteins and acute phase reactant proteins in children with sickle cell anemia.

Authors:  R P Warrier; S Kuvibidila; L Gordon; J Humbert
Journal:  J Natl Med Assoc       Date:  1994-01       Impact factor: 1.798

6.  Factors associated with lowered intelligence in homozygous sickle cell disease.

Authors:  S Knight; A Singhal; P Thomas; G Serjeant
Journal:  Arch Dis Child       Date:  1995-10       Impact factor: 3.791

7.  Acceleration in linear growth after splenectomy for hypersplenism in homozygous sickle cell disease.

Authors:  A Singhal; P Thomas; T Kearney; S Venugopal; G Serjeant
Journal:  Arch Dis Child       Date:  1995-03       Impact factor: 3.791

8.  Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease.

Authors:  Claudia R Morris; Jung H Suh; Ward Hagar; Sandra Larkin; D Anton Bland; Martin H Steinberg; Elliott P Vichinsky; Mark Shigenaga; Bruce Ames; Frans A Kuypers; Elizabeth S Klings
Journal:  Blood       Date:  2007-09-11       Impact factor: 22.113

9.  An anthropometric and hematological comparison of sickle cell disease children from rural and urban areas.

Authors:  H S Nikhar; S U Meshram; G B Shinde
Journal:  Indian J Hum Genet       Date:  2012-01

10.  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
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