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与白血病前期综合征相关的难治性铁粒幼细胞贫血中的血红素生物合成

Haem biosynthesis in refractory sideroblastic anaemia associated with the preleukaemic syndrome.

作者信息

Pasanen A V, Vuopio P, Borgström G H, Tenhunen R

出版信息

Scand J Haematol. 1981 Jul;27(1):35-44. doi: 10.1111/j.1600-0609.1981.tb00449.x.

Abstract

The activities of 5 enzymes of the haem biosynthetic pathway and the protoporphyrin concentrations have been measured in peripheral red blood cells of 23 patients having a preleukaemic syndrome with refractory sideroblastic anaemia. A decreased delta-aminolaevulinic acid synthase (ALA-S) activity, an increased uroporphyrinogen I synthase activity and an increased red cell protoporphyrin concentration were consistent findings. Patients with abnormal leucocyte and/or platelet counts in the peripheral blood as well as patients with an excess of blast cells in the bone marrow had the lowest ALA-S activities. A further decrease in ALA-S activity was observed in 3 patients after leukaemic change in the disease. Patients having cytogenetic abnormalities showed no unique enzyme abnormalities. These results indicate that enzymatic disturbances of haem synthesis cannot be used as prognostic indicator of leukaemic transformation in refractory sideroblastic anaemia, but a very low ALA-S activity appears to accompany the development of a leukaemia in such patients.

摘要

在23例患有难治性铁粒幼细胞贫血的白血病前期综合征患者的外周血红细胞中,测定了血红素生物合成途径中5种酶的活性和原卟啉浓度。一致的发现是,δ-氨基乙酰丙酸合成酶(ALA-S)活性降低、尿卟啉原Ⅰ合成酶活性增加以及红细胞原卟啉浓度增加。外周血白细胞和/或血小板计数异常的患者以及骨髓中原始细胞过多的患者,其ALA-S活性最低。在3例疾病发生白血病变化后的患者中,观察到ALA-S活性进一步降低。有细胞遗传学异常的患者未表现出独特的酶异常。这些结果表明,血红素合成的酶紊乱不能用作难治性铁粒幼细胞贫血白血病转化的预后指标,但在这类患者中,极低的ALA-S活性似乎伴随着白血病的发生。

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