Hepcidin Levels in Sickle Cell Disease (SCD)
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|ClinicalTrials.gov Identifier: NCT02258997|
Recruitment Status : Completed
First Posted : October 8, 2014
Last Update Posted : October 8, 2015
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The investigators propose that patients with HbSβ-thalassemia have lower levels of hepcidin and higher levels of GDF-15 than HbSS patients during the non-crisis, "steady states." In addition, the investigators propose that when controlled for RBC transfusion, patients with HbSβ-thalassemia will have higher levels of storage iron (based on serum ferritin).
Participants: Total number of subjects is 42 - 21 subjects with HbSS, and 21 subjects with HbSβ-thalassemia ).
Procedures (methods): Eligible subjects with documented SCD (HbSS, HbS-β 0-thalassemia or HbS-β+-thalassemia) followed at the University of North Carolina (UNC) Comprehensive Sickle Cell Program will be evaluated in this single-center, prospective, cross-sectional study. The patients will be screened for eligibility at the time of a routine sickle cell clinic visit. Patients' data will be obtained in person at the time of evaluation and through review of their medical records. Investigators will obtain information on SCD-related clinical complications and obtain an estimate of the number of lifetime RBC transfusions. Blood samples will be obtained for laboratory tests. Plasma samples for hepcidin, growth differentiation factor 15 (GDF -15), and high-sensitivity CRP will be stored at -80 degrees Celsius until analysis. Other routine laboratory studies including complete blood count (CBC) with differential and reticulocyte count, serum iron profile and ferritin, and liver function tests will be performed at the clinical laboratories of UNC Hospitals.The subjects will have 30 ml. of blood drawn for this research study. Females of child bearing potential will have a urine pregnancy test at the time of the study.
|Condition or disease|
|Sickle Cell Anemia Sickle - Beta Thalassemia|
Sickle cell disease (SCD) refers to a group of inherited disorders characterized by the presence of sickle hemoglobin (HbS) that are associated with episodes of acute illness and progressive organ damage. The most common variant of SCD, sickle cell anemia (HbSS), refers to homozygosity for the β S allele, with most of the remaining patients having sickle hemoglobin C disease (HbSC) and sickle beta thalassemia (HbSβ-thalassemia).
SCD may be associated with iron overload that occurs following repeated red blood cell (RBC) transfusions. However, in patients with beta thalassemia major, iron overload occurs due to both repeated RBC transfusions and hyperabsorption of iron. The hyperabsorption of iron in beta thalassemia occurs due to ineffective erythropoiesis and subsequent downregulation of hepcidin. Thalassemia intermedia and major are the most studied human models of hepcidin modulation by ineffective erythropoiesis alone and the combined and opposite effect of both ineffective erythropoiesis and transfusion dependent iron overload, accordingly. Regular transfusions induce massive iron loading but inhibit erythropoietic drive. Accordingly, hepcidin production is higher in thalassemia major than in thalassemia intermedia although still inappropriate to the massive transfusional iron loading that partially counteracts the erythropoietic-dependent hepcidin down-regulation (Origa R et al, 2007; Kattamis A et al, 2006; Camberlein E et al, 2008). No differences in the steady-state levels of hepcidin was observed when HbSS patients (N = 40) were compared with healthy hemoglobin AA (HbAA)controls (N = 30) (85.3 ± 30 l μg/L vs. 83.5 ± 40 l μg/L) (Ezeh C et al, 2005).
Hepcidin is a 25-amino acid peptide produced mainly in the liver and is the major physiological regulator of body iron stores and serum iron. It negatively regulates egress of iron from cells, such as intestinal epithelial cells and macrophages. Growth differentiation factor-15 (GDF-15) and twisted gastrulation protein homolog 1(TWSG1), two transforming growth factor-β (TGF-β) superfamily members released from erythroid precursors, have been proposed to contribute to hepcidin suppression in thalassemia, although it remains unresolved whether GDF-15 and TWSG1 are markers of ineffective erythropoiesis or mediators of hepcidin suppression in vivo.
With the presence of a thalassemia gene, patients with HbSβ-thalassemia (HbSβ0-thalassemia and HbSβ+-thalassemia) may have an increased tendency to absorb excess iron compared to patients with HbSS.
|Study Type :||Observational|
|Actual Enrollment :||42 participants|
|Official Title:||Hepcidin Levels in Sickle Cell Disease (SCD)|
|Study Start Date :||March 2014|
|Actual Primary Completion Date :||September 2015|
|Actual Study Completion Date :||September 2015|
Subjects are homozygous for the sickle hemoglobin mutation (HbS).
Subjects are heterozygous for the HbS mutation and beta thalassemia
- Hepcidin levels in HbSS and HbSβ-thalassemia SCD patients [ Time Frame: Assessed at time of enrollment ]
- Levels of GDF-15 in HbSS and HbSβ-thalassemia SCD patients [ Time Frame: Assessed at time of enrollment ]
- Ferritin and C-reactive protein (CRP) levels in SCD patients in the non-crisis state [ Time Frame: Assessed at time of enrollment ]
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|Ages Eligible for Study:||18 Years to 70 Years (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
|Sampling Method:||Non-Probability Sample|
- age 18 - 70 years
- confirmed diagnosis of HbSS or HbS-β thalassemia
- no history of acute vaso-occlusive event (acute pain crisis or acute chest syndrome) requiring emergency room visit or hospitalization over the preceding 4 weeks
- clinically acceptable physical examination and vital signs
- ability of patient or legal representative to understand the requirements of the study and willingness to sign the Informed Consent document.
- pregnancy or breastfeeding
- current acute illness, including a painful crisis
- iron deficiency anemia
- history of liver disease with alanine aminotransferase (ALT) ≥ 3 X upper limit of normal (ULN)
- history of hereditary hemochromatosis, connective tissues disease, chronic inflammatory, disorder, or malignancy
- chronic transfusion program or any transfusion within the previous 3 months
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02258997
|Principal Investigator:||Kenneth I Ataga, MBBS||University of North Carolina, Chapel Hill|
|Responsible Party:||Kenneth Ataga, MD, Associate Professor of Medicine, Director, University of North Carolina (UNC) Comprehensive Sickle Cell Program, University of North Carolina, Chapel Hill|
|Other Study ID Numbers:||
|First Posted:||October 8, 2014 Key Record Dates|
|Last Update Posted:||October 8, 2015|
|Last Verified:||October 2014|
sickle cell disease
Anemia, Sickle Cell
Anemia, Hemolytic, Congenital
Genetic Diseases, Inborn