| Literature DB >> 29433052 |
Yuta Baba1, Bungo Saito2, Shotaro Shimada2, Yohei Sasaki2, So Murai2, Maasa Abe2, Shun Fujiwara2, Nana Arai2, Yukiko Kawaguchi2, Nobuyuki Kabasawa2, Hiroyuki Tsukamoto2, Yui Uto2, Hirotsugu Ariizumi2, Kouji Yanagisawa2, Norimichi Hattori2, Hiroshi Harada2, Tsuyoshi Nakamaki2.
Abstract
Studies showed red cell distribution width (RDW) can improve the detection of morphological changes in red blood cells and the understanding of their contribution to dyserythropoiesis in myelodysplastic syndrome (MDS). The purpose of the study was to evaluate dyserythropoiesis in MDS by RDW analysis and to explore the utility of RDW in clinical practice. We retrospectively analyzed laboratory and clinical data of 101 patients (59 patients was refractory anemia (RA) according to the French-American-British (FAB) classification). In patients with RA, RDW was showed weak inverse correlation with both hemoglobin concentration (Hb) (rs = -0.37, P = 0.0035) and mean corpuscular hemoglobin concentration (MCHC) (rs = -0.36, P = 0.0047). On the other hand, RDW was showed weak correlation with the number of ringed sideroblasts in bone marrow (rs = 0.31, P = 0.023). The increased RDW (≥15.0%) was associated with shorter overall survival (OS) (P = 0.0086). In patients with refractory anemia with excess blasts (RAEB) and RAEB in transformation (RAEB-t), effect of RDW on OS was less evident. These results suggested that increased RDW might reflect dyserythropoiesis, associated with deregulated hemoglobin synthesis and iron metabolism in MDS. Furthermore, increased RDW may have potential to be a prognostic significance in RA.Entities:
Keywords: Dyserythropoiesis; Myelodysplastic syndromes; Red cell distribution width; Refractory anemia
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Year: 2018 PMID: 29433052 DOI: 10.1016/j.leukres.2018.02.004
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156