Literature DB >> 14982264

Concentrations of B vitamins and homocysteine in children with sickle cell anemia.

Jodi B Segal1, Edgar R Miller, Nga Hong Brereton, Linda M S Resar.   

Abstract

BACKGROUND: Elevated concentration of serum homocysteine contributes to thrombosis, a frequent event in patients with sickle cell anemia. We aimed to test whether children with sickle cell anemia have elevated concentrations of serum homocysteine with diminished levels of folate or B vitamins from accelerated blood cell turnover.
METHODS: We conducted a case-control study of children with homozygous sickle cell anemia (n = 17) and unaffected children (n = 11). We measured serum and red blood cell folate, vitamin B6, vitamin B12, and homocysteine concentrations, and assessed micronutrient intake.
RESULTS: Children with sickle cell anemia had concentrations of homocysteine slightly higher than those of unaffected children. They had lower vitamin B6 concentrations and comparable concentrations of folate and vitamin B12. Homocysteine concentration was inversely related to vitamin B12 concentration and was not independently associated with levels of vitamin B6 or folate.
CONCLUSION: Despite comparable intake, children with sickle cell anemia had lower concentrations of vitamin B6 than unaffected children. Larger studies are needed to determine if chronically low serum vitamin B6 concentration contributes to hyperhomocysteinemia in this population.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14982264     DOI: 10.1097/01.SMJ.0000051740.56511.93

Source DB:  PubMed          Journal:  South Med J        ISSN: 0038-4348            Impact factor:   0.954


  9 in total

1.  Trace elements in children suffering from sickle cell anemia: A case-control study.

Authors:  Joseph K Sungu; Olivier Mukuku; Augustin Mulangu Mutombo; Paul Mawaw; Michel N Aloni; Oscar N Luboya
Journal:  J Clin Lab Anal       Date:  2017-02-15       Impact factor: 2.352

2.  Cobalamin status in sickle cell disease.

Authors:  O I Ajayi; S Bwayo-Weaver; S Chirla; M Serlemitsos-Day; M Daniel; M Nouraie; K Edwards; O Castro; F Lombardo; V R Gordeuk
Journal:  Int J Lab Hematol       Date:  2012-07-26       Impact factor: 2.877

3.  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

4.  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

5.  Copper status in patients with thalassemia major in zahedan, iran.

Authors:  Mohamad Ali Mashhadi
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2013

6.  The prevalence of zinc deficiency in patients with thalassemia in South East of iran, sistan and baluchistan province.

Authors:  Mohammad Ali Mashhadi; Zahra Sepehri; Zahra Heidari; Eghbal Shirzaee; Zohre Kiani
Journal:  Iran Red Crescent Med J       Date:  2014-08-05       Impact factor: 0.611

Review 7.  Phytomedicines and nutraceuticals: alternative therapeutics for sickle cell anemia.

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

8.  Selenium and Vitamin E as antioxidants in chronic hemolytic anemia: Are they deficient? A case-control study in a group of Egyptian children.

Authors:  Mona M Hamdy; Dalia S Mosallam; Alaa M Jamal; Walaa A Rabie
Journal:  J Adv Res       Date:  2015-01-13       Impact factor: 10.479

9.  Dietary intakes and nutritional status of children with sickle cell disease at the Princess Marie Louise Hospital, Accra - a survey.

Authors:  Isaac Boadu; Agartha Ohemeng; Lorna Awo Renner
Journal:  BMC Nutr       Date:  2018-08-23
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.