Catechol-O-Methyltransferase Polymorphisms Predict Opioid Consumption in Postoperative Pain

被引:54
作者
Candiotti, Keith A. [1 ]
Yang, Zhe [1 ]
Buric, David [1 ]
Arheart, Kris [1 ]
Zhang, Yanping [1 ]
Rodriguez, Yiliam [1 ]
Gitlin, Melvin C. [1 ]
Carvalho, Enisa [1 ]
Jaraba, Isabel [1 ]
Wang, Liyong [1 ]
机构
[1] Univ Miami, Sch Med, Dept Anesthesiol Perioperat Med & Pain Management, Miami, FL 33101 USA
关键词
MORPHINE REQUIREMENTS; GENE POLYMORPHISMS; CANCER-PATIENTS; COMT GENE; MICE; ANALGESIA; RESPONSES;
D O I
10.1213/ANE.0000000000000411
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
BACKGROUND: Previous studies have associated the catechol-O-methyltransferase (COMT) enzyme rs4680 polymorphism with opioid consumption in the treatment of chronic cancer pain. In this study, we evaluated the association between COMT rs4680 and rs4818 polymorphisms and opioid consumption in the acute postoperative period after a nephrectomy. METHODS: Opioid consumption and pain scores were evaluated in 152 patients for 48 hours after nephrectomy. The genotype of each patient was determined using polymerase chain reaction on DNA extracted from blood samples. The association between rs4680 and rs4818 genotypes and opioid consumption was evaluated using general linear model regression analysis. All P values and confidence intervals were Bonferroni corrected for the 3 comparisons among genotypes. RESULTS: In the 24-hour period after surgery (COMT rs4680), patients homozygous for the variant Val/Val consumed 36% (95% confidence interval, 31%-41%) more opioids than patients homozygous for the Met/Met group (P = 0.009). No statistically significant differences among the 3 genotype groups were noted for pain scores or emesis medication use in the first 24 hours after surgery. There was a statistically significant increase in emesis medication use in patients possessing the CC genotype of rs4818 when compared to patients carrying the GG genotypes (P = 0.035). In the 6- to 48-hour postsurgery period, there was significantly higher opioid consumption in the high-activity homozygotes Val/Val than in the homozygous Met/Met group for COMT rs4680 (0-6 h: P = 0.005; 0-12 h: P = 0.015; 0-24 h: P = 0.015; and 0-48 h: P = 0.023). Patients in the homozygous GG group COMT rs4818 single nucleotide polymorphism showed statistically significant differences in opioid consumption in the first 6 hours after nephrectomy compared with heterozygous CG patients (P = 0.02). CONCLUSIONS: The genetic variant of the COMT rs4680 single nucleotide polymorphism is associated with variability in opioid consumption in postoperative nephrectomy patients. The COMT rs4818 polymorphism may prove useful in predicting emesis medication use postoperatively.
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收藏
页码:1194 / 1200
页数:7
相关论文
共 18 条
[1]
Polymorphism in the Interleukin-1 Receptor Antagonist Gene Is Associated with Serum Interleukin-1 Receptor Antagonist Concentrations and Postoperative Opioid Consumption [J].
Candiotti, Keith A. ;
Yang, Zongqi ;
Morris, Richard ;
Yang, Jinfeng ;
Crescimone, Nicolas A. ;
Sanchez, Greys C. ;
Bird, Vincent ;
Leveillee, Raymond ;
Rodriguez, Yiliam ;
Liu, Huanliang ;
Zhang, Yu Dana ;
Bethea, John R. ;
Gitlin, Melvin C. .
ANESTHESIOLOGY, 2011, 114 (05) :1162-1168
[2]
Environmental and genetic factors associated with morphine response in the postoperative period [J].
Coulbault, L ;
Beaussier, M ;
Verstuyft, C ;
Weickmans, H ;
Dubert, L ;
Trégouet, D ;
Descot, C ;
Parc, Y ;
Lienhart, A ;
Jaillon, P ;
Becquemont, L .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2006, 79 (04) :316-324
[3]
Genetic basis for individual variations in pain perception and the development of a chronic pain condition [J].
Diatchenko, L ;
Slade, GD ;
Nackley, AG ;
Bhalang, K ;
Sigurdsson, A ;
Belfer, I ;
Goldman, D ;
Xu, K ;
Shabalina, SA ;
Shagin, D ;
Max, MB ;
Makarov, SS ;
Maixner, W .
HUMAN MOLECULAR GENETICS, 2005, 14 (01) :135-143
[4]
Catechol-O-methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior [J].
Gogos, JA ;
Morgan, M ;
Luine, V ;
Santha, M ;
Ogawa, S ;
Pfaff, D ;
Karayiorgou, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (17) :9991-9996
[5]
The Associations Between OPRM1 and COMT Genotypes and Postoperative Pain, Opioid Use, and Opioid-Induced Sedation [J].
Henker, Richard A. ;
Lewis, Allison ;
Dai, Feng ;
Lariviere, William R. ;
Meng, Li ;
Gruen, Gary S. ;
Sereika, Susan M. ;
Pape, Hans ;
Tarkin, Ivan S. ;
Gowda, Indira ;
Conley, Yvette P. .
BIOLOGICAL RESEARCH FOR NURSING, 2013, 15 (03) :309-317
[6]
Stress-induced analgesia and morphine responses are changed in catechol-O-methyltransferase-deficient male mice [J].
Kambur, Oleg ;
Mannisto, Pekka T. ;
Viljakka, Kaarin ;
Reenila, Ilkka ;
Lemberg, Kim ;
Kontinen, Vesa K. ;
Karayiorgou, Maria ;
Gogos, Joseph A. ;
Kalso, Eija .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2008, 103 (04) :367-373
[7]
Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans [J].
Kim, Hyungsuk ;
Lee, Hyewon ;
Rowan, Janet ;
Brahim, Jaime ;
Dionne, Raymond A. .
MOLECULAR PAIN, 2006, 2
[8]
Combined Catechol-O-Methyltransferase and μ-Opioid Receptor Gene Polymorphisms Affect Morphine Postoperative Analgesia and Central Side Effects [J].
Kolesnikov, Yuri ;
Gabovits, Boris ;
Levin, Ariel ;
Voiko, Edward ;
Veske, Andres .
ANESTHESIA AND ANALGESIA, 2011, 112 (02) :448-453
[9]
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders [J].
Lachman, HM ;
Papolos, DF ;
Saito, T ;
Yu, YM ;
Szumlanski, CL ;
Weinshilboum, RM .
PHARMACOGENETICS, 1996, 6 (03) :243-250
[10]
Catecholamine-O-Methyltransferase Polymorphisms Are Associated With Postoperative Pain Intensity [J].
Lee, Peter J. ;
Delaney, Patrick ;
Keogh, John ;
Sleeman, Duncan ;
Shorten, George D. .
CLINICAL JOURNAL OF PAIN, 2011, 27 (02) :93-101