Literature DB >> 23066366

Sickle cell anemia: iron availability and nocturnal oximetry.

Sharon E Cox1, Veline L'Esperance, Julie Makani, Deogratius Soka, Andrew M Prentice, Catherine M Hill, Fenella J Kirkham.   

Abstract

STUDY
OBJECTIVE: To test the hypothesis that low iron availability, measured as transferrin saturation, is associated with low nocturnal hemoglobin oxygen saturation (SpO(2)) in children with homozygous sickle cell anemia (SCA; hemoglobin SS).
METHODS: This was a cross-sectional study of Tanzanian children with SCA who were not receiving regular blood transfusions. Thirty-two children (16 boys) with SCA (mean age 8.0, range 3.6-15.3 years) underwent motion-resistant nocturnal oximetry (Masimo Radical) and had steady state serum transferrin saturation and hematological indices assessed.
RESULTS: Higher transferrin saturation, adjusted for age and α-thalassemia deletion, was associated with lower nocturnal mean SpO(2) (p = 0.013, r(2) = 0.41), number of SpO(2) dips/h > 3% from baseline (p = 0.008, r(2) = 0.19) and with min/h with SpO(2) < 90% (p = 0.026 r(2) = 0.16). Transferrin saturation < 16% (indicative of iron deficiency) was associated with a 2.2% higher nocturnal mean SpO(2).
CONCLUSIONS: Contrary to our hypothesis, higher iron availability, assessed by transferrin saturation, is associated with nocturnal chronic and intermittent hemoglobin oxygen desaturation in SCA. Whether these associations are causal and are driven by hypoxia-inducible factor and hepcidin-mediated upregulation of demand for iron warrants further investigation.

Entities:  

Keywords:  Africa; anemia; hemoglobin saturation; hypoxemia; iron; sickle cell

Mesh:

Substances:

Year:  2012        PMID: 23066366      PMCID: PMC3459200          DOI: 10.5664/jcsm.2152

Source DB:  PubMed          Journal:  J Clin Sleep Med        ISSN: 1550-9389            Impact factor:   4.062


  18 in total

1.  Effect of alpha-globin genotype on the pathophysiology of sickle cell disease.

Authors:  S K Ballas
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Authors:  J P Needleman; M E Franco; L Varlotta; D Reber-Brodecki; N Bauer; C Dampier; J L Allen
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Review 4.  Hypoxic adaptation during development: relation to pattern of neurological presentation and cognitive disability.

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Journal:  Dev Sci       Date:  2006-07

Review 5.  Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes.

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Journal:  Blood Rev       Date:  2006-11-07       Impact factor: 8.250

6.  Iron deficiency and sleep disordered breathing in children--cause or effect?

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7.  Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology.

Authors:  B N Yamaja Setty; Marie J Stuart; Carlton Dampier; Darcy Brodecki; Julian L Allen
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8.  Daytime steady-state haemoglobin desaturation is a risk factor for overt stroke in children with sickle cell anaemia.

Authors:  Charles T Quinn; James W Sargent
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9.  Improvement of sickle cell anemia by iron-limited erythropoiesis.

Authors:  O Castro; W N Poillon; H Finke; E Massac
Journal:  Am J Hematol       Date:  1994-10       Impact factor: 10.047

10.  Mortality in sickle cell anemia in Africa: a prospective cohort study in Tanzania.

Authors:  Julie Makani; Sharon E Cox; Deogratius Soka; Albert N Komba; Julie Oruo; Hadija Mwamtemi; Pius Magesa; Stella Rwezaula; Elineema Meda; Josephine Mgaya; Brett Lowe; David Muturi; David J Roberts; Thomas N Williams; Kisali Pallangyo; Jesse Kitundu; Gregory Fegan; Fenella J Kirkham; Kevin Marsh; Charles R Newton
Journal:  PLoS One       Date:  2011-02-16       Impact factor: 3.240

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2.  Hematological and Genetic Predictors of Daytime Hemoglobin Saturation in Tanzanian Children with and without Sickle Cell Anemia.

Authors:  Sharon E Cox; Julie Makani; Charles R Newton; Andrew M Prentice; Fenella J Kirkham
Journal:  ISRN Hematol       Date:  2013-04-03

Review 3.  Review on iron and its importance for human health.

Authors:  Nazanin Abbaspour; Richard Hurrell; Roya Kelishadi
Journal:  J Res Med Sci       Date:  2014-02       Impact factor: 1.852

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