Erythropoietic drive is the strongest predictor of hepcidin level in adults with sickle cell disease. Blood Cells Mol Dis 2015 Dec;55(4):304-7
Date
10/16/2015Pubmed ID
26460251Pubmed Central ID
PMC4754107DOI
10.1016/j.bcmd.2015.07.010Scopus ID
2-s2.0-84943574815 (requires institutional sign-in at Scopus site) 17 CitationsAbstract
Levels of hepcidin, a key modulator of iron metabolism, are influenced by erythropoiesis, iron, and inflammation, all of which may be increased in patients with sickle cell disease (SCD). The objectives of this study were to determine: 1) the variation in hepcidin level, and 2) the relative contribution of erythropoietic drive, iron, and inflammation to differences in hepcidin level in an adult cohort with SCD. In a prospective study, cross-sectional measurements of hepcidin, reticulocyte percentage, erythropoietin, ferritin, and high-sensitivity CRP were obtained. A regression tree analysis was used to measure the association between these interacting factors and hepcidin level. The cohort was comprised of 40 adults with SCD. Median age was 26years, 68% were female, and all had HbSS. Hepcidin values ranged from 30ng/ml to 326ng/ml, with a median of 87ng/ml. Regression tree analysis demonstrated that reticulocyte percentage, erythropoietin, ferritin and hs-CRP all were associated with hepcidin. The highest hepcidin values were found in subjects with low reticulocyte percentage and erythropoietin. In conclusion, erythropoietic drive, iron status, and inflammation all contribute to variation in hepcidin level. The strongest contributor is erythropoietic drive. Future studies could determine whether suppression of erythropoiesis with chronic transfusion influences hepcidin level.
Author List
Karafin MS, Koch KL, Rankin AB, Nischik D, Rahhal G, Simpson P, Field JJAuthors
Joshua J. Field MD Professor in the Medicine department at Medical College of WisconsinKathryn L. Koch NP APP Hybrid in the Medicine department at Medical College of Wisconsin
Pippa M. Simpson PhD Adjunct Professor in the Pediatrics department at Medical College of Wisconsin
MESH terms used to index this publication - Major topics in bold
AdultAnemia, Sickle Cell
Cross-Sectional Studies
Erythropoiesis
Female
Hepcidins
Humans
Male
Middle Aged
Young Adult
