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Journal ArticleDOI

The pharmacogenetics of codeine pain relief in the postpartum period.

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TLDR
Findings will assist in customizing therapy to effectively manage postpartum pain by examining select genetic polymorphisms in the codeine pharmacological pathway.
Abstract
The objective of this study was to examine interindividual variability in codeine requirements and pain management by examining select genetic polymorphisms in the codeine pharmacological pathway. The study included a nested cohort of 98 women who were prescribed codeine following cesarean section. Participants were genotyped for select polymorphisms of the COMT, ABCB1, CYP2D6, UGT2B7 and OPRM1 genes and instructed to describe their level of pain using the visual analog scale (mm) 1 h following each dose of codeine. Analysis revealed that reported pain increases with maternal age (P=0.041). Asians required more codeine than Caucasians (P=0.048). Significant differences in mean dose consumption were seen among the genotypic groups of the OPRM1 A118G (P=0.001) and UGT2B7 C802T (P=0.015) variants. These variants were found to predict codeine consumption in the cohort overall (P=0.000) and among Caucasians (P=0.001). These findings will assist in customizing therapy to effectively manage postpartum pain.

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Journal ArticleDOI

Review of Opioid Pharmacogenetics and Considerations for Pain Management

TL;DR: The influence of polymorphisms in pharmacokinetics genes, as well as pharmacodynamics genes (OPRM1 and COMT) on response to opioids has been a subject of intense research, and the results have been somehow conflicting.

Codeine Therapy and CYP2D6 Genotype

Laura Dean
TL;DR: In contrast, individuals who carry more than two normal function copies of the CYP2D6 gene (ultrarapid metabolizers) are able to metabolize codeine to morphine more rapidly and more completely as discussed by the authors.
Journal ArticleDOI

Pharmacogenomics for Primary Care: An Overview

TL;DR: The potential utility of PGx in primary care will be explored and on-going barriers to implementation discussed and the evidence base of several drug-gene pairs relevant to primary care relevant to antidepressants, codeine and tramadol, statins, clopidogrel, warfarin, metoprolol and allopurinol are outlined.
Journal ArticleDOI

Pharmacogenomics in Pain Management

TL;DR: Several cytochrome enzymes have been found to be involved with ketamine but there is no strong evidence of individual polymorphisms manifesting in clinical outcomes.
Journal ArticleDOI

Pharmacogenetics of opioids: a narrative review

TL;DR: An in‐depth knowledge of single‐nucleotide polymorphisms can help clinicians to address interindividual variability in opioid dosing and requirements and can also help to design prognostic tools to accurately predict the analgesic dose of opioids.
References
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Journal ArticleDOI

Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo

TL;DR: A significant correlation of a polymorphism in exon 26 (C3435T) of MDR-1 with expression levels and function is observed and this polymorphism is expected to affect the absorption and tissue concentrations of numerous other substrates of M DR-1.
Journal ArticleDOI

Codeine intoxication associated with ultrarapid CYP2D6 metabolism.

TL;DR: CYP2D6 genotyping showed that the patient had three or more functional alleles, a finding consistent with ultrarapid metabolism of codeine, and attribute the toxicity to this genotype in combination with inhibition of CYP3A4 activity by other medications and a transient reduction in renal function.
Journal ArticleDOI

Allelic expression imbalance of human mu opioid receptor (OPRM1) caused by variant A118G.

TL;DR: In this article, the authors measured allele-specific mRNA expression of OPRM1 in human autopsy brain tissues, using A118G as a marker, and found that the A118 mRNA allele was 1.5-2.5 times more abundant than the G118 allele.
Journal ArticleDOI

The Val158Met polymorphism of the human catechol-O-methyltransferase (COMT) gene may influence morphine requirements in cancer pain patients.

TL;DR: The results suggest that genetic variation in the COMT gene may contribute to variability in the efficacy of morphine in cancer pain treatment.
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