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The relationship between fetal hemoglobin level and glycosylation in sickle cell disease.

作者信息

Elseweidy M M, Abraham E C

出版信息

Am J Hematol. 1984 May;16(4):375-81. doi: 10.1002/ajh.2830160408.

DOI:10.1002/ajh.2830160408
PMID:6202137
Abstract

Glycosylated hemoglobin (glyco Hb) was determined by affinity chromatography and Hb S1 and Hb F by Bio-Rex 70 chromatography in patients with sickle cell anemia, SC disease, S beta+-thalassemia, and S beta 0-thalassemia. SC and S beta-thalassemia patients had normal levels of glyco Hb whereas SS patients had significantly lower levels. Within each group of patients a direct correlation existed between Hb F and glyco Hb or Hb S1 levels. A similar relationship was noticed when glyco Hb and Hb F levels were compared in red cell populations of various densities (ages). Hb F seems to influence glycosylation through its effect on red cell survival.

摘要

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