Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6, OPRM1, and COMT genotype and select opioid therapy
Opioids are mainly used to treat both acute and chronic pain. Several opioids are metabolized to some extent by CYP2D6 (codeine, tramadol, hydrocodone, oxycodone and methadone). Polymorphisms in CYP2D6 have been studied for an association with the clinical effect and safety of these drugs. Other gen...
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Veröffentlicht in: | Clinical pharmacology and therapeutics 2021-02, Vol.110 (4), p.888-896 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Opioids are mainly used to treat both acute and chronic pain. Several opioids are metabolized to some extent by CYP2D6 (codeine, tramadol, hydrocodone, oxycodone and methadone). Polymorphisms in
CYP2D6
have been studied for an association with the clinical effect and safety of these drugs. Other genes which have been studied for their association with opioid clinical effect or adverse events include
OPRM1
(mu receptor) and
COMT
(catechol-O-methyltransferase). This guideline updates and expands the 2014 Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for
CYP2D6
genotype and codeine therapy and includes a summation of the evidence describing the impact of
CYP2D6
,
OPRM1
and
COMT
on opioid analgesia and adverse events. We provide therapeutic recommendations for the use of
CYP2D6
genotype results for prescribing codeine and tramadol and describe the limited and/or weak data for
CYP2D6
and hydrocodone, oxycodone and methadone and for
OPRM1
and
COMT
for clinical use. |
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ISSN: | 0009-9236 1532-6535 |
DOI: | 10.1002/cpt.2149 |