HYDRATION OF RED-CELLS IN ALPHA-THALASSEMIA AND BETA-THALASSEMIA DIFFERS - A USEFUL APPROACH TO DISTINGUISH BETWEEN THESE RED-CELL PHENOTYPES

被引:19
|
作者
BUNYARATVEJ, A
FUCHAROEN, S
GREENBAUM, A
MOHANDAS, N
机构
[1] UNIV CALIF BERKELEY,LAWRENCE BERKELEY LAB,DIV LIFE SCI,BERKELEY,CA 94720
[2] MAHIDOL UNIV,RAMATHIBODI HOSP,DEPT PATHOL,BANGKOK 10700,THAILAND
[3] MAHIDOL UNIV,FAC MED,CTR THALALASSEMIA,BANGKOK,THAILAND
[4] MILES DIAGNOST,TARRYTOWN,NY
关键词
CELL HEMOGLOBIN CONCENTRATION; CELL VOLUME; HEMOGLOBINOPATHIES; RED CELL INDEXES; RED CELLS; THALASSEMIA;
D O I
10.1093/ajcp/102.2.217
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Differences in the pathobiologic features of alpha and beta thalassemic red cells include differing derangements in the ability of these cells to regulate their volume. To explore differences in cell hydration in these two red cell phenotypes, heterogeneity in hemoglobin concentration of individual red cells was quantitated. Red cells from 91 patients with alpha thalassemia (hemoglobin H disease) and 69 patients with beta thalassemia of the genotype beta-thal zero/Hb E were analyzed. Marked differences between these thalassemias were noted in the heterogeneity of hemoglobin concentration among individual cells. Decreased cell hemoglobin concentration and increased cell hydration were features of alpha-thalassemic blood samples, whereas both decreased and increased cell hemoglobin concentration as a result of cell hydration and dehydration, respectively, were features of beta-thalassemic blood samples. The documented differences in the hemoglobin concentration distributions should prove useful in distinguishing between the two thalassemic phenotypes.
引用
收藏
页码:217 / 222
页数:6
相关论文
共 50 条
  • [1] KINETIC ALTERATIONS OF THE RED-CELL MEMBRANE PHOSPHATASE IN ALPHA-THALASSEMIA AND BETA-THALASSEMIA
    MORLE, L
    DORLEAC, E
    ALLOISIO, N
    JACCOUD, P
    COLONNA, P
    BACHIR, D
    DELAUNAY, J
    AMERICAN JOURNAL OF HEMATOLOGY, 1982, 13 (04) : 269 - 282
  • [2] RED-CELL INDEXES AND ALPHA-THALASSEMIA
    SONATI, MD
    KIMURA, EM
    COSTA, FF
    REVISTA BRASILEIRA DE GENETICA, 1992, 15 (03): : 687 - 693
  • [3] ALPHA-THALASSEMIA AND BETA-THALASSEMIA TRAITS - BIOLOGICAL DIFFERENCE BASED ON RED-CELL INDEXES AND ZINC PROTOPORPHYRIN
    HAN, P
    FUNG, KP
    TEO, CP
    TAM, LP
    CLINICAL AND LABORATORY HAEMATOLOGY, 1990, 12 (02): : 169 - 176
  • [4] A MOLECULAR ABNORMALITY OF RED-CELL MEMBRANE IN BETA-THALASSEMIA
    MORLE, F
    MORLE, L
    AGUERCIF, M
    ALLOISIO, N
    DELAUNAY, J
    COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES, 1980, 174 (04): : 598 - 604
  • [5] CHANGES OF RED-CELL PHOSPHOLIPIDS IN BETA-THALASSEMIA MINOR
    KALOFOUTIS, A
    DISKAKIS, E
    STRATAKIS, NJ
    PAPADEMETRIOU, A
    BIOCHEMICAL MEDICINE, 1980, 23 (01): : 1 - 5
  • [6] RED-CELL MEMBRANE ABNORMALITIES IN BETA-THALASSEMIA MAJOR
    RICEEVANS, C
    JOHNSON, A
    FLYNN, DM
    FEBS LETTERS, 1980, 119 (01) : 53 - 57
  • [7] RED-CELL GENETIC ABNORMALITIES IN PENINSULAR ARABS - SICKLE HEMOGLOBIN, G6PD DEFICIENCY, AND ALPHA-THALASSEMIA AND BETA-THALASSEMIA
    WHITE, JM
    BYRNE, M
    RICHARDS, R
    BUCHANAN, T
    KATSOULIS, E
    WEERASINGH, K
    JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) : 245 - 251
  • [8] CHARACTERIZATION AND COMPARISON OF THE RED-BLOOD-CELL MEMBRANE DAMAGE IN SEVERE HUMAN ALPHA-THALASSEMIA AND BETA-THALASSEMIA
    ADVANI, R
    SORENSON, S
    SHINAR, E
    LANDE, W
    RACHMILEWITZ, E
    SCHRIER, SL
    BLOOD, 1992, 79 (04) : 1058 - 1063
  • [9] USE OF RED-CELL DISTRIBUTION WIDTH AND ERYTHROCYTE ZINC PROTOPORPHYRIN IN DIFFERENTIAL-DIAGNOSIS OF ALPHA-THALASSEMIA AND BETA-THALASSEMIA AND IRON-DEFICIENCY
    TILLYER, ML
    TILLYER, CR
    JOURNAL OF CLINICAL PATHOLOGY, 1994, 47 (03) : 205 - 208
  • [10] RED-CELL FERRITIN AND IRON OVERLOAD IN HETEROZYGOUS BETA-THALASSEMIA
    VANDERWEYDEN, MB
    FONG, H
    HALLAM, LJ
    HARRISON, C
    AMERICAN JOURNAL OF HEMATOLOGY, 1989, 30 (04) : 201 - 205