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80例非亲缘性迟发性皮肤卟啉病患者的红细胞尿卟啉原脱羧酶活性

Erythrocyte uroporphyrinogen decarboxylase activity in 80 unrelated patients with porphyria cutanea tarda.

作者信息

Kószó F, Morvay M, Dobozy A, Simon N

机构信息

Department of Dermatology, Albert Szent-Györgyi Medical University, Szeged, Hungary.

出版信息

Br J Dermatol. 1992 May;126(5):446-9. doi: 10.1111/j.1365-2133.1992.tb11816.x.

Abstract

To estimate the prevalence of the subgroups of porphyria cutanea tarda (PCT), erythrocyte uroporphyrinogen decarboxylase (UD) activity was measured in 80 unrelated patients with PCT, and in 45 of their relatives by using pentacarboxyl-porphyrinogen III as substrate. The subgroups were differentiated by analysis of the urinary porphyrins of the patients and 119 of their relatives. Of the patients, 77.5% were found to be suffering from the sporadic form of PCT (type I PCT), and 22.5% from the familial form (type II PCT). Every patient with PCT had previously been affected by alcohol, oestrogen or some other liver-damaging factor. The relative frequency of familial PCT was higher in females (nine of 15) than in males (nine of 65), which suggests that inheritance of the gene for type II PCT may predispose to oestrogen-precipitated PCT. The onset of type II PCT occurred at a lower age than that of type I (42.6 vs. 47.0 years). The findings suggest an increased risk of precipitating factors in carriers of an inherited UD deficiency.

摘要

为了评估迟发性皮肤卟啉症(PCT)各亚组的患病率,以五羧基卟啉原III为底物,对80例无亲缘关系的PCT患者及其45名亲属的红细胞尿卟啉原脱羧酶(UD)活性进行了测定。通过分析患者及其119名亲属的尿卟啉来区分亚组。在这些患者中,发现77.5%患有散发性PCT(I型PCT),22.5%患有家族性PCT(II型PCT)。每位PCT患者此前都曾受到酒精、雌激素或其他一些肝损伤因素的影响。家族性PCT在女性中的相对频率(15例中的9例)高于男性(65例中的9例),这表明II型PCT基因的遗传可能易导致雌激素诱发的PCT。II型PCT的发病年龄低于I型(42.6岁对47.0岁)。这些发现表明,遗传性UD缺乏携带者中诱发因素的风险增加。

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