Literature DB >> 22486937

Is ethnicity associated with morphine's side effects in children? Morphine pharmacokinetics, analgesic response, and side effects in children having tonsillectomy.

Nathalia Jimenez1, Gail D Anderson, Danny D Shen, Susan S Nielsen, Federico M Farin, Kristy Seidel, Anne M Lynn.   

Abstract

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.
BACKGROUND: 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.
METHODS: 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.
RESULTS: 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.
CONCLUSIONS: 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.
© 2012 Blackwell Publishing Ltd.

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Year:  2012        PMID: 22486937      PMCID: PMC3366036          DOI: 10.1111/j.1460-9592.2012.03844.x

Source DB:  PubMed          Journal:  Paediatr Anaesth        ISSN: 1155-5645            Impact factor:   2.556


  24 in total

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Review 2.  Genetic variability and clinical efficacy of morphine.

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3.  Pharmacogenetic impact of polymorphisms in the coding region of the UGT1A1 gene on SN-38 glucuronidation in Japanese patients with cancer.

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Authors:  J L Galinkin; L M Fazi; R M Cuy; R M Chiavacci; C D Kurth; U K Shah; I N Jacobs; M F Watcha
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6.  Association of ABCB1/MDR1 and OPRM1 gene polymorphisms with morphine pain relief.

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9.  Ethnicity and OPRM variant independently predict pain perception and patient-controlled analgesia usage for post-operative pain.

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  10 in total

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Review 2.  Racial and Ethnic Disparities in Adverse Drug Events: A Systematic Review of the Literature.

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3.  Genetics of pain perception, COMT and postoperative pain management in children.

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4.  Beneficial effects of dexmedetomidine on early postoperative cognitive dysfunction in pediatric patients with tonsillectomy.

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5.  Prospective observational pharmacogenetic study of side effects induced by intravenous morphine for postoperative analgesia.

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6.  Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits.

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8.  Association Between Race and Ethnicity with Intraoperative Analgesic Administration and Initial Recovery Room Pain Scores in Pediatric Patients: a Single-Center Study of 21,229 Surgeries.

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9.  The Influence of Genotype Polymorphism on Morphine Analgesic Effect for Postoperative Pain in Children.

Authors:  Mi Geum Lee; Hyun Jung Kim; Keun Hwa Lee; Yun Suk Choi
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Review 10.  Pharmacogenomics and Morphine.

Authors:  Adaku Ofoegbu; Earl B Ettienne
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  10 in total

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