Analysis of Hereditary Elliptocytosis with Decreased Binding of Eosin-5-maleimide to Red Blood Cells

• Published in: BioMed research international Vol. 2015; no. 2015; pp. 1 - 6
• Main Authors: Sugihara, Takashi, Tsujioka, Takayuki, Nakanishi, Hidekazu, Wada, Hideho, Suemori, Shin-ichiro, Tohyama, Kaoru
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 01-01-2015; John Wiley & Sons, Inc; Hindawi Limited
• Subjects: Blood; Case-Control Studies; Elliptocytosis, Hereditary - metabolism; Eosine Yellowish-(YS) - analogs & derivatives; Eosine Yellowish-(YS) - metabolism; Erythrocytes; Erythrocytes - metabolism; Flow Cytometry - methods; Genetic disorders; Hemolytic anemia; Humans; Medical schools; Morphology; Mutation; Physiological aspects; Proteins; Scanning electron microscopy; Sensitivity and Specificity; Set design
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2015/451861

Flow cytometric test for analyzing the eosin-5-maleimide (EMA) binding to red blood cells has been believed to be a specific method for diagnosing hereditary spherocytosis (HS). However, it has been reported that diseases other than HS, such as hereditary pyropoikilocytosis (HPP) and Southeast Asian ovalocytosis (SAO), which are forms in the category of hereditary elliptocytosis (HE), show decreased EMA binding to red blood cells. We analyzed EMA binding to red blood cells in 101 healthy control subjects and 42 HS patients and obtained a mean channel fluorescence (MCF) cut-off value of 36.4 (sensitivity 0.97, specificity 0.95). Using this method, we also analyzed 12 HE patients. Among them, four HE patients showed the MCF at or below the cut-off value. It indicates that some HE patients have decreased EMA binding to red blood cells. Two of these four HE patients were classified as common HE, and two were spherocytic HE with reduced spectrin. This study demonstrates that, in addition to patients with HPP or SAO, some HE patients have decreased EMA binding to red blood cells.