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葡萄糖-6-磷酸脱氢酶缺乏症患儿接受氨苯砜治疗后溶血性贫血的临床谱和严重程度。

Clinical spectrum and severity of hemolytic anemia in glucose 6-phosphate dehydrogenase-deficient children receiving dapsone.

机构信息

GlaxoSmithKline, Brentford, TW8 9GS, London, United Kingdom.

出版信息

Blood. 2012 Nov 15;120(20):4123-33. doi: 10.1182/blood-2012-03-416032. Epub 2012 Sep 19.

Abstract

Drug-induced acute hemolytic anemia led to the discovery of G6PD deficiency. However, most clinical data are from isolated case reports. In 2 clinical trials of antimalarial preparations containing dapsone (4,4'-diaminodiphenylsulfone; 2.5 mg/kg once daily for 3 days), 95 G6PD-deficient hemizygous boys, 24 G6PD-deficient homozygous girls, and 200 girls heterozygous for G6PD deficiency received this agent. In the first 2 groups, there was a maximum decrease in hemoglobin averaging -2.64 g/dL (range -6.70 to +0.30 g/dL), which was significantly greater than for the comparator group receiving artemether-lumefantrine (adjusted difference -1.46 g/dL; 95% confidence interval -1.76, -1.15). Hemoglobin concentrations were decreased by ≥ 40% versus pretreatment in 24/119 (20.2%) of the G6PD-deficient children; 13/119 (10.9%) required blood transfusion. In the heterozygous girls, the mean maximum decrease in hemoglobin was -1.83 g/dL (range +0.90 to -5.20 g/dL); 1 in 200 (0.5%) required blood transfusion. All children eventually recovered. All the G6PD-deficient children had the G6PD A- variant, ie, mutations V68M and N126D. Drug-induced acute hemolytic anemia in G6PD A- subjects can be life-threatening, depending on the nature and dosage of the drug trigger. Therefore, contrary to current perception, in clinical terms the A- type of G6PD deficiency cannot be regarded as mild. This study is registered at http://www.clinicaltrials.gov as NCT00344006 and NCT00371735.

摘要

药物诱导的急性溶血性贫血导致了 G6PD 缺乏症的发现。然而,大多数临床数据来自于孤立的病例报告。在 2 项含有氨苯砜(4,4'-二氨基二苯砜;每天 2.5mg/kg,连用 3 天)的抗疟制剂的临床试验中,95 名 G6PD 缺乏症半合子男孩、24 名 G6PD 缺乏症纯合子女孩和 200 名 G6PD 缺乏症杂合子女孩接受了该药物。在前 2 组中,血红蛋白的最大下降平均为-2.64g/dL(范围为-6.70 至+0.30g/dL),明显大于接受青蒿琥酯-甲氟喹治疗的对照组(调整后的差异为-1.46g/dL;95%置信区间-1.76,-1.15)。与治疗前相比,24/119(20.2%)名 G6PD 缺乏症儿童的血红蛋白降低≥40%;13/119(10.9%)需要输血。在杂合子女孩中,血红蛋白的最大平均下降为-1.83g/dL(范围为+0.90 至-5.20g/dL);200 名女孩中有 1 名(0.5%)需要输血。所有儿童最终都康复了。所有 G6PD 缺乏症儿童均具有 G6PD A- 变异型,即突变 V68M 和 N126D。G6PD A- 个体的药物诱导性急性溶血性贫血可能危及生命,具体取决于药物触发的性质和剂量。因此,与目前的认知相反,从临床角度来看,G6PD A- 型缺乏症不能被视为轻度。该研究在 http://www.clinicaltrials.gov 注册,编号为 NCT00344006 和 NCT00371735。

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