Department of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, California, USA.
Family Center for Research with Ubuntu, Department of Paediatrics and Child Health, Stellenbosch University and Tygerberg Hospital, Cape Town, South Africa.
Clin Infect Dis. 2022 Sep 29;75(6):1037-1045. doi: 10.1093/cid/ciac001.
Isoniazid (INH) metabolism depends on the N-acetyl transferase 2 (NAT2) enzyme, whose maturation process remains unknown in low birth weight (LBW) and preterm infants. We aimed to assess INH exposure and safety in infants receiving oral tuberculosis prevention.
This population pharmacokinetics (PK) analysis used INH and N-acetyl-isoniazid (ACL) concentrations in infants (BW ≤ 4 kg), including preterm, with follow-up for 6 months. PK parameters were described using nonlinear mixed effects modeling. Simulations were performed to assess INH exposure and optimal dosing regimens, using 2 targets: Cmax at 3-6 mg/L and area under the curve (AUC) ≥ 10.52 mg h/L.
We included 57 infants (79% preterm, 84% LBW) in the PK analysis, with a median (range) gestational age of 34 (28.7-39.4) weeks. At the time of sampling, postnatal age was 2.3 (0.2-7.3) months and weight (WT) was 3.7 (0.9-9.3) kg. NAT2 genotype was available in 43 (75.4%) patients (10 slow, 26 intermediate, and 7 fast metabolizers). Ninety percent of NAT2 maturation was attained by 4.4 post-natal months. WT, postmenstrual age, and NAT2 genotype significantly influenced INH exposure, with a 5-fold difference in AUC between slow and fast metabolizers for the same dose. INH appeared safe across the broad range of exposure for 61 infants included in the safety analysis.
In LBW/preterm infants, INH dosing needs frequent adjustment to account for growth and maturation. Pharmacogenetics-based dosing regimens is the most powerful approach to deliver safe and equalized exposures for all infants, because NAT2 genotype highly impacts INH pharmacokinetic variability.
异烟肼(INH)的代谢依赖于 N-乙酰转移酶 2(NAT2)酶,其成熟过程在低出生体重(LBW)和早产儿中尚不清楚。我们旨在评估接受口服结核病预防的婴儿中 INH 的暴露和安全性。
本群体药代动力学(PK)分析使用了包括早产儿在内的 BW≤4kg 的婴儿的 INH 和 N-乙酰异烟肼(ACL)浓度,随访时间为 6 个月。使用非线性混合效应模型描述 PK 参数。使用 2 个目标进行模拟,以评估 INH 的暴露和最佳给药方案:Cmax 为 3-6mg/L 和 AUC≥10.52mg·h/L。
我们纳入了 57 名 PK 分析患儿(79%早产儿,84%LBW),中位(范围)胎龄为 34(28.7-39.4)周。在采样时,出生后年龄为 2.3(0.2-7.3)个月,体重(WT)为 3.7(0.9-9.3)kg。43 名(75.4%)患者的 NAT2 基因型可用(10 名慢代谢者,26 名中间代谢者,7 名快代谢者)。90%的 NAT2 成熟在出生后 4.4 个月达到。WT、孕周和 NAT2 基因型显著影响 INH 暴露,相同剂量下慢代谢者和快代谢者的 AUC 差异达 5 倍。在纳入安全性分析的 61 名婴儿中,INH 表现出良好的安全性。
在 LBW/早产儿中,INH 剂量需要频繁调整,以考虑生长和成熟。基于药物遗传学的剂量方案是为所有婴儿提供安全和均等暴露的最有力方法,因为 NAT2 基因型高度影响 INH 药代动力学变异性。