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儿童呼吸道结核治疗中异烟肼的药代动力学

Isoniazid pharmacokinetics in children treated for respiratory tuberculosis.

作者信息

Schaaf H S, Parkin D P, Seifart H I, Werely C J, Hesseling P B, van Helden P D, Maritz J S, Donald P R

机构信息

Department of Paediatrics and Child Health, Faculty of Health Sciences, Stellenbosch University, Tygerberg Children's Hospital, South Africa.

出版信息

Arch Dis Child. 2005 Jun;90(6):614-8. doi: 10.1136/adc.2004.052175.

Abstract

AIMS

To define the pharmacokinetics of isoniazid (INH) in children with tuberculosis in relation to the N-acetyltransferase 2 (NAT2) genotype.

METHODS

The first order elimination rate constant (k) and area under the concentration curve (AUC) were calculated in 64 children <13 years of age (median 3.8) with respiratory tuberculosis from INH concentrations determined 2-5 hours after a 10 mg/kg INH dose. The NAT2 genotype was determined; 25 children were classified as homozygous slow (SS), 24 as heterozygous fast (FS), and 15 as homozygous fast (FF) acetylators.

RESULTS

The mean (SD) k values of the genotypes differed significantly from one another: SS 0.254 (0.046), FS 0.513 (0.074), FF 0.653 (0.117). Within each genotype a median regression of k on age showed a significant decrease in k with age. The mean (SD) INH concentrations (mg/l) two hours after INH administration were SS 8.599 (1.974), FS 5.131 (1.864), and FF 3.938 (1.754). A within genotype regression of 2-hour INH concentrations on age showed a significant increase with age. A within genotype regression of 3-hour, 4-hour, and 5-hour concentrations on age also showed a significant increase with age in each instance. In ethnically similar adults, mean (SD) 2-hour INH concentrations (mg/l) for each genotype were significantly higher than the children's: SS 10.942 (1.740), FS 8.702 (1.841), and FF 6.031 (1.431).

CONCLUSIONS

Younger children eliminate INH faster than older children and, as a group, faster than adults, and require a higher mg/kg body weight INH dose to achieve serum concentrations comparable to adults.

摘要

目的

确定异烟肼(INH)在患有结核病的儿童体内的药代动力学与N - 乙酰转移酶2(NAT2)基因型的关系。

方法

对64名13岁以下(中位数3.8岁)患有呼吸道结核病的儿童,在给予10mg/kg异烟肼剂量后2 - 5小时测定异烟肼浓度,计算一级消除速率常数(k)和浓度曲线下面积(AUC)。确定NAT2基因型;25名儿童被分类为纯合慢乙酰化者(SS),24名为杂合快乙酰化者(FS),15名为纯合快乙酰化者(FF)。

结果

各基因型的平均(标准差)k值彼此有显著差异:SS为0.254(0.046),FS为0.513(0.074),FF为0.653(0.117)。在每种基因型中,k对年龄的中位数回归显示k随年龄显著降低。异烟肼给药后两小时的平均(标准差)异烟肼浓度(mg/l)分别为:SS 8.599(1.974),FS 5.131(1.864),FF 3.938(1.754)。两小时异烟肼浓度对年龄的基因型内回归显示随年龄显著增加。三小时、四小时和五小时浓度对年龄的基因型内回归在每种情况下也显示随年龄显著增加。在种族相似的成年人中,每种基因型的平均(标准差)两小时异烟肼浓度(mg/l)显著高于儿童:SS 10.942(1.740),FS 8.702(1.841),FF 6.031(1.431)。

结论

年幼儿童比年长儿童更快消除异烟肼,并且作为一个群体,比成年人更快,并且需要更高的mg/kg体重异烟肼剂量才能达到与成年人相当的血清浓度。

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引用本文的文献

本文引用的文献

1
The chemical approach to the control of tuberculosis.控制结核病的化学方法。
Science. 1952 Aug 8;116(3006):129-34. doi: 10.1126/science.116.3006.129.
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Genetic control of isoniazid metabolism in man.人体中异烟肼代谢的遗传控制。
Br Med J. 1960 Aug 13;2(5197):485-91. doi: 10.1136/bmj.2.5197.485.
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Isoniazid pharmacokinetics in children according to acetylator phenotype.
Fundam Clin Pharmacol. 2001 Oct;15(5):355-9. doi: 10.1046/j.1472-8206.2001.00044.x.
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Isoniazid acetylation metabolic ratio during maturation in children.儿童发育过程中异烟肼乙酰化代谢率
Clin Pharmacol Ther. 1997 Oct;62(4):377-83. doi: 10.1016/S0009-9236(97)90115-6.

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