Balevic Stephen J, Becker Mara L, Gonzalez Daniel, Funk Ryan S
J Pediatr Pharmacol Ther. 2021;26(8):809-814. doi: 10.5863/1551-6776-26.8.809. Epub 2021 Nov 10.
To evaluate the impact of obesity on etanercept (ETN) drug exposure in children with juvenile idiopathic arthritis (JIA).
We conducted a pilot, cross-sectional, observational study in a real-world cohort of children with JIA receiving ETN as standard of care from a single center. We analyzed the relationship between body size and ETN plasma concentrations, adjusting for dosage. Body size was analyzed as a continuous measure using weight and body mass index (BMI) percentiles and categorically using BMI percentile classifications according to the CDC guidelines.
We enrolled a total of 29 children. Each child provided one plasma sample for ETN concentration measurement, and all participants were receiving subcutaneous ETN dosed weekly. We observed that the ETN concentration normalized for dose decreased significantly as a function of weight (p = 0.004) and BMI percentile (p = 0.04). Similarly, we observed a progressive decline in mean and median dose-normalized concentrations across higher body size categories. Because of reaching maximum ETN dosage (50 mg), 7 of 8 children (87.5%) with obesity received a weight-based dosage < 0.8 mg/kg/dose.
We found that higher body weight and BMI percentile are significantly and negatively associated with ETN drug serum concentration, accounting for differences in dosing. Our data suggest that children who are obese may be routinely under-dosed using current dosing strategies. Inadequate dosing may increase the risk for therapeutic failure and long-term morbidity in a developing child. As a result, characterizing adequate drug exposure in children of all sizes is an important step toward precision dosing.
评估肥胖对幼年特发性关节炎(JIA)患儿使用依那西普(ETN)药物暴露的影响。
我们在一个来自单一中心的、接受ETN作为标准治疗的JIA患儿真实队列中开展了一项试点横断面观察性研究。我们分析了体型与ETN血浆浓度之间的关系,并对剂量进行了校正。体型作为连续变量使用体重和体重指数(BMI)百分位数进行分析,作为分类变量则根据美国疾病控制与预防中心(CDC)指南使用BMI百分位数分类进行分析。
我们共纳入了29名儿童。每个儿童提供一份用于测量ETN浓度的血浆样本,所有参与者均接受每周一次皮下注射ETN治疗。我们观察到,经剂量校正后的ETN浓度随体重(p = 0.004)和BMI百分位数(p = 0.04)的增加而显著降低。同样,我们观察到,随着体型类别增加,平均和中位数剂量校正浓度呈逐渐下降趋势。由于达到了ETN最大剂量(50 mg),8名肥胖儿童中有7名(87.5%)接受的基于体重的剂量<0.8 mg/kg/剂量。
我们发现较高的体重和BMI百分位数与ETN药物血清浓度显著负相关,这解释了剂量差异。我们的数据表明,肥胖儿童使用当前的给药策略可能经常剂量不足。剂量不足可能会增加发育中儿童治疗失败和长期发病的风险。因此,确定所有体型儿童的充足药物暴露量是实现精准给药的重要一步。