The Impact of CYP2D6 Genetic Polymorphisms on Postoperative Morphine Consumption

  1. Keith A. Candiotti MD1,*,
  2. Zongqi Yang MD, PhD1,
  3. Yiliam Rodriguez MD1,
  4. Andres Crescimone MD1,
  5. Greys C. Sanchez MD1,
  6. Peter Takacs MD, PhD2,
  7. Carlos Medina MD2,
  8. Yanping Zhang PhD1,
  9. Huanliang Liu MD, PhD3,
  10. Melvin C. Gitlin MD1

Article first published online: 11 JUN 2009

DOI: 10.1111/j.1526-4637.2009.00641.x

Issue

Pain Medicine

Pain Medicine

Volume 10, Issue 5, pages 799–805, July/August 2009

Additional Information

How to Cite

Candiotti, K. A., Yang, Z., Rodriguez, Y., Crescimone, A., Sanchez, G. C., Takacs, P., Medina, C., Zhang, Y., Liu, H. and Gitlin, M. C. (2009), The Impact of CYP2D6 Genetic Polymorphisms on Postoperative Morphine Consumption. Pain Medicine, 10: 799–805. doi: 10.1111/j.1526-4637.2009.00641.x

Author Information

  1. 1

    Department of Anesthesiology, Perioperative Medicine and Pain Management;

  2. 2

    Department of Obstetrics and Gynecology;

  3. 3

    Department of Microbiology and Immunology, University of Miami, Miller School of Medicine, Miami, Florida, USA

*Keith Candiotti, MD, University of Miami School of Medicine, Jackson Memorial Hospital Department of Anesthesiology, Perioperative Medicine and Pain Management (R-370), 1611 Northwest 12th Avenue, Miami, FL 33101, USA. Tel: 305-585-5332; Fax: 305-585-7002; E-mail: kcandiotti@miami.edu.

Publication History

  1. Issue published online: 28 JUL 2009
  2. Article first published online: 11 JUN 2009

SEARCH

SEARCH BY CITATION

ARTICLE TOOLS

View Full Article (HTML) Get PDF (130K)

Keywords:

  • CYP2D6;
  • Genetic Polymorphisms;
  • Postoperative Pain;
  • Morphine Consumption;
  • Ultrarapid CYP2D6 Metabolizers

ABSTRACT

Background.  Endogenous morphine-like compounds have been identified in humans and are released in response to stress. Human monocytes and granulocytes express the µ opiate receptor, µ3, which is morphine selective but opiate peptide insensitive. Recent studies have shown that CYP2D6 acts at critical steps for endogenous morphine biosynthesis. We theorized that ultrarapid (UM) CYP2D6 metabolizers may have an enhancement of their endogenous pain modulating mechanisms.

Methods.  After institutional review board approval, a previously developed surgical patient database was evaluated for information concerning CYP2D6 genotypes and morphine consumption. One hundred forty-two patients were found to have adequate information to be included in this current analysis. The study group was divided, based on morphine consumption, into two subgroups: low morphine consumers (LMC) (≤10 mg/4 h, N = 80) and high morphine consumers (HMC) (>10 mg/4 h, N = 62). DNA was extracted from blood in all patients and was genotyped by the Amplichip (Roche, Pleasanton, CA) to determine the specific CYP2D6 genotypes.

Results.  CYP2D6 UM were found to occur more frequently in the LMC group than in the HMC group (8/80 vs 0/62, P = 0.0091). No significant differences were noted for the poor, intermediate, or extensive metabolizers.

Conclusions.  Our current results suggest that CYP2D6 UM appear to require less morphine in the acute postoperative period compared with other CYP2D6 metabolizer groups. One possible mechanism for this observation is that CYP2D6 UM may have higher efficiency in synthesizing endogenous morphine compared with other metabolizers, thus increasing endogenous pain modulation and reducing the need for exogenous morphine.

View Full Article (HTML) Get PDF (130K)