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1.
Monography in French | AIM (Africa) | ID: biblio-1275346

Subject(s)
Anemia , Hematology , Review
9.
Acta Haematol ; 61(1): 15-26, 1979.
Article in English | MEDLINE | ID: mdl-105535

ABSTRACT

The simplified Hb A2 determination based on microchromatography in Pasteur pipets filled with DEAE-cellulose with glycine-KCN-NaCl as developers [14] is compared with a reference Hb A2 determination procedure based on starch-block electrophoresis. The utility of microchromatography as a routine Hb A2 assay and as a screening method to detect beta-thalassemia trait carriers and patients with iron deficiency anemia was investigated. Day-to-day variation of a control hemolysate and the correlation between the values obtained with the two methods and between determinations in duplicate on the same sample are given. The mean values obtained with both methods for the different groups do not differ significantly but the standard deviations and the coefficients of variation observed by the microchromatography are generally higher. Microchromatography in Pasteur pipets tends to overestimate low and normal Hb A2 concentrations and to underestimate high Hb A2 concentrations. The results of microchromatography are more significant for the diagnosis when Hb A2 concentrations are expressed in weight hemoglobin per volume of blood and not in percentages. The microchromatographic procedure was recently marketed. The results obtained with the commercial columns were in good correlation with those obtained with starch-block electrophoresis, but commercial columns give a 18% overestimation of the Hb A2 concentrations.


Subject(s)
Anemia, Hypochromic/diagnosis , Chromatography, DEAE-Cellulose/methods , Electrophoresis, Starch Gel/methods , Hemoglobin A2/analysis , Hemoglobin A/analysis , Thalassemia/diagnosis , Adult , Anemia, Hypochromic/blood , Chromatography, DEAE-Cellulose/instrumentation , Evaluation Studies as Topic , Humans , Thalassemia/blood , Thalassemia/genetics
10.
Am J Trop Med Hyg ; 27(4): 659-63, 1978 Jul.
Article in English | MEDLINE | ID: mdl-686238

ABSTRACT

The influence of malaria on the hemoglobin A2 (Hb A2) level in humans was studied in a series of 94 imported cases in Belgium. Sixty-nine of the patients were natives of Western European countries, their results are reported separately since their origin and the results of their hematological examination made it unlikely that they carried the beta-thalassemia trait. The Hb A2 level of the 94 malaria patients (mean 2.76%; S.D. 0.51%) was not statistically different from that found in 60 healthy controls (mean 2.70%; S.D. 0.38%; P greater than 40). Likewise the level of the 65 Western European patients was not statistically different from that of the same controls (mean 2.81%; S.D. 0.42%; P greater than 0.10). There was also no significant difference between the level in patients infected with a particular species of Plasmodium and that of the controls. No correlation was found between the Hb A2 level and the intensity of the parasitemia or the concentration of total hemoglobin in the blood. These results are discussed in comparison with the divergent ones obtained by others and it is suggested that malaria has no significant influence on the results of surveys for the prevalence of beta-thalassemia in regions of malaria endemicity.


Subject(s)
Hemoglobin A/analysis , Hemoglobins/analysis , Malaria/blood , Adult , Humans , Thalassemia/blood
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