Jimenez Nathalia, Anderson Gail D, Shen Danny D, Nielsen Susan S, Farin Federico M, Seidel Kristy, Lynn Anne M
Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, WA, USA.
Paediatr Anaesth. 2012 Jul;22(7):669-75. doi: 10.1111/j.1460-9592.2012.03844.x. Epub 2012 Apr 4.
OBJECTIVES/AIMS: To examine whether morphine pharmacokinetics (PK) and/or genetic polymorphisms in opioid-related genes, underlie differences in analgesic response and side effects to morphine in Latino (L) vs non-Latino Caucasian (NL) children.
Morphine has high interindividual variability in its analgesic response and side effects profile. Earlier studies suggest that morphine response may vary by race and ethnicity.
Prospective cohort study in L and NL children, 3-17 years of age comparing pain scores, occurrence of side effects, plasma morphine, morphine-6- and morphine-3-glucuronide concentrations measured after a single morphine IV bolus administration. Noncompartmental pharmacokinetic analysis and genotyping for 28 polymorphisms in eight genes (UGT1A8, UGT2B7, ABCB1, COMT, STAT6, MC1R, OPRM1, and ARRB2) were performed.
We enrolled 68 children (33 L, 35 NL). There were no differences in pain scores or need for rescue analgesia. Statistically significant differences in the occurrence of side effects were documented: While 58% of L children experienced at least one side effect only 20% of NL did (P = 0.001). Pruritus was four times (P = 0.006) and emesis seven times (P = 0.025) more frequent in L compared with NL. PK parameters were similar between groups. None of the assessed polymorphisms mediated the association between ethnicity and side effects.
We found statistically significant differences in the occurrence of side effects after morphine administration between L and NL children. Neither differences in morphine or metabolite concentrations, nor the genetic polymorphisms examined explain these findings. Studies are needed to further investigate reasons for the increase in morphine side effects by Latino ethnicity.
研究在拉丁裔(L)与非拉丁裔白种人(NL)儿童中,吗啡药代动力学(PK)和/或阿片类相关基因的遗传多态性是否是导致对吗啡镇痛反应和副作用存在差异的原因。
吗啡的镇痛反应和副作用具有较高的个体间变异性。早期研究表明,吗啡反应可能因种族和民族而异。
对3至17岁的L族和NL族儿童进行前瞻性队列研究,比较单次静脉注射吗啡后测得的疼痛评分、副作用发生率、血浆吗啡、吗啡-6-葡萄糖醛酸苷和吗啡-3-葡萄糖醛酸苷浓度。进行了非房室药代动力学分析以及对八个基因(UGT1A8、UGT2B7、ABCB1、COMT、STAT6、MC1R、OPRM1和ARRB2)中的28个多态性进行基因分型。
我们纳入了68名儿童(33名L族,35名NL族)。疼痛评分或急救镇痛需求方面没有差异。记录到副作用发生率存在统计学显著差异:58%的L族儿童至少经历过一种副作用,而NL族儿童只有20%(P = 0.001)。与NL族相比,L族的瘙痒发生率高出四倍(P = 0.006),呕吐发生率高出七倍(P = 0.025)。两组之间的PK参数相似。所评估的多态性均未介导种族与副作用之间的关联。
我们发现L族和NL族儿童在注射吗啡后副作用发生率存在统计学显著差异。吗啡或代谢物浓度的差异以及所检测的基因多态性均无法解释这些发现。需要开展研究以进一步探究拉丁裔种族导致吗啡副作用增加的原因。