Literature DB >> 10524455

Physiologic decline in fetal hemoglobin parameters in infants with sickle cell disease: implications for pharmacological intervention.

S J Marcus1, R E Ware.   

Abstract

PURPOSE: Fetal hemoglobin (HbF) is an important determinant in the clinical severity of patients with sickle cell disease. The physiologic decline in HbF parameters in a cohort of infants with sickle cell disease was investigated. PATIENTS AND METHODS: The percent HbF and F cells were quantitated, and the HbF per F cell was then calculated. One hundred thirty-eight blood samples from 44 infants with homozygous sickle cell anemia (HbSS) and 56 samples from 24 infants with sickle cell hemoglobin (HbSC) were studied.
RESULTS: Infants with HbSS had a logarithmic decline in HbF parameters; at 24 months, the average HbF was 14.6%+/-7.3% and the % F cells was 64.7%+/-16.9%. The amount of HbF in each F cell (HbF per F cell) was <15 pg/cell, a suggested threshold for intracellular sickle polymerization, by age 12 months. Infants with HbSC had a more rapid decline: at 12 months the average % HbF was 12.2%+/-9.3%, the % F cells was 60.5%+/-18.7%, and the HbF per F cell was <10 pg/cell.
CONCLUSIONS: By age 2 years, HbF parameters including the % HbF, % F cells, and the HbF per F cell decrease to levels insufficient to inhibit sickling. Pharmacologic intervention designed to enhance HbF production and prevent chronic organ damage should be considered during infancy.

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Year:  1999        PMID: 10524455     DOI: 10.1097/00043426-199909000-00013

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  10 in total

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2.  Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.

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3.  A clinically meaningful fetal hemoglobin threshold for children with sickle cell anemia during hydroxyurea therapy.

Authors:  Jeremie H Estepp; Matthew P Smeltzer; Guolian Kang; Chen Li; Winfred C Wang; Christina Abrams; Banu Aygun; Russell E Ware; Kerri Nottage; Jane S Hankins
Journal:  Am J Hematol       Date:  2017-09-28       Impact factor: 10.047

Review 4.  How I use hydroxyurea to treat young patients with sickle cell anemia.

Authors:  Russell E Ware
Journal:  Blood       Date:  2010-03-11       Impact factor: 22.113

5.  Expression patterns of fetal hemoglobin in sickle cell erythrocytes are both patient- and treatment-specific during childhood.

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6.  Reticulocyte parameters and hemoglobin F production in sickle cell disease patients undergoing hydroxyurea therapy.

Authors:  R Borba; C S P Lima; H Z W Grotto
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Review 7.  Changing the Clinical Paradigm of Hydroxyurea Treatment for Sickle Cell Anemia Through Precision Medicine.

Authors:  Min Dong; Patrick T McGann
Journal:  Clin Pharmacol Ther       Date:  2020-10-08       Impact factor: 6.875

Review 8.  Hydroxycarbamide: clinical aspects.

Authors:  Russell E Ware
Journal:  C R Biol       Date:  2012-11-09       Impact factor: 1.583

Review 9.  High Foetal Haemoglobin in Sickle Cell Disease: Not so Protective?

Authors:  Nicola Conran
Journal:  EBioMedicine       Date:  2015-01-14       Impact factor: 8.143

10.  Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia.

Authors:  Emily R Meier; Susan E Creary; Matthew M Heeney; Min Dong; Abena O Appiah-Kubi; Stephen C Nelson; Omar Niss; Connie Piccone; Maa-Ohui Quarmyne; Charles T Quinn; Kay L Saving; John P Scott; Ravi Talati; Teresa S Latham; Amanda Pfeiffer; Lisa M Shook; Alexander A Vinks; Adam Lane; Patrick T McGann
Journal:  Trials       Date:  2020-11-27       Impact factor: 2.279

  10 in total

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