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3.
Blut ; 61(4): 245-7, 1990 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-2145991

RESUMO

To evaluate the platelet function in sickle cell syndromes we measured the beta-thromboglobulin (beta-TG) and platelet factor 4 (PF-4) plasma values of 45 patients suffering from homozygous sickle cell anaemia (10) and sickle cell beta-thalassaemia (35) in steady state. The results were compared to those of 32 normal controls. Both the beta-TG and PF-4 levels were found to be significantly higher in patients than in controls but the beta-TG:PF-4 ratio was significantly lower in the patients group. This finding and the absence of any statistical correlation between platelet number and beta-TG or PF-4 indicate that platelets seem to be somehow activated in sickle cell syndromes, both in homozygotes and sickle cell/beta-thalassaemia heterozygotes. This platelet activation seems to exist even in steady state sickle cell disease patients, regardless of the functional status of the spleen.


Assuntos
Anemia Falciforme/metabolismo , Fator Plaquetário 4/análise , beta-Tromboglobulina/análise , Adolescente , Adulto , Idoso , Anemia Falciforme/genética , Feminino , Heterozigoto , Homozigoto , Humanos , Masculino , Pessoa de Meia-Idade
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