Oshikoya K A, Sammons H, Smith K, Choonara I
Academic Division of Child Health, Graduate Entry Medical School in Derby, University of Nottingham, Derby, UK Department of Pharmacology, Lagos State University College of Medicine, Ikeja, Lagos, Nigeria.
Academic Division of Child Health, Graduate Entry Medical School in Derby, University of Nottingham, Derby, UK.
Arch Dis Child. 2015 Jul;100(7):689-93. doi: 10.1136/archdischild-2014-308017. Epub 2015 Apr 20.
Limited data from pharmacokinetic studies in underweight and severely malnourished children have indicated an impaired activity of their hepatic enzymes. We used the caffeine breath test to assess the metabolising activity of cytochrome P450 1A2 (CYP1A2) enzyme in underweight children.
Underweight children from the paediatric outpatient clinic, Lagos State University Teaching Hospital, Ikeja in Nigeria, were studied. After an overnight fast, 15 underweight children took 3 mg/kg labelled caffeine orally. Breath samples were collected in duplicate at -20, -10 and -1 min and at 15 min intervals for 2 h. The mean cumulative per cent dose recovered (CPDR) of labelled caffeine in the expired carbon dioxide was determined over the study period. This was repeated after 2-6 weeks of nutritional rehabilitation.
The mean areas under the enrichment-time curve before and after nutritional rehabilitation were 0.539±0.320 and 0.620±0.322 atom per cent excess minute, respectively. The difference between the two values was not statistically significant (p=0.528). The mean CPDR in the exhaled carbon dioxide of the underweight children over a period of 2 h was 7.56±4.01% and 7.95±3.68% before and after nutritional rehabilitation, respectively, and there was no significant difference in the mean values (p=0.603).
The metabolism of caffeine was not significantly affected in underweight children compared with after 2-6 weeks of nutritional rehabilitation. This suggests that hepatic CYP1A2-metabolising activity was not significantly impaired in underweight children.
来自体重不足和严重营养不良儿童药代动力学研究的有限数据表明,他们的肝酶活性受损。我们使用咖啡因呼气试验来评估体重不足儿童细胞色素P450 1A2(CYP1A2)酶的代谢活性。
对尼日利亚伊凯贾拉各斯州立大学教学医院儿科门诊的体重不足儿童进行了研究。在禁食过夜后,15名体重不足的儿童口服3mg/kg标记咖啡因。在-20、-10和-1分钟以及之后2小时内每隔15分钟重复采集呼气样本。在研究期间测定呼出二氧化碳中标记咖啡因的平均累积剂量回收百分比(CPDR)。在营养康复2-6周后重复此操作。
营养康复前后富集-时间曲线下的平均面积分别为0.539±0.320和0.620±0.322原子百分比过量分钟。这两个值之间的差异无统计学意义(p=0.528)。体重不足儿童在2小时内呼出二氧化碳中的平均CPDR在营养康复前后分别为7.56±4.01%和7.95±3.68%,平均值无显著差异(p=0.603)。
与营养康复2-6周后相比,体重不足儿童的咖啡因代谢未受到显著影响。这表明体重不足儿童的肝脏CYP1A2代谢活性未受到显著损害。