The mu opioid receptor A118G gene polymorphism moderates effects of trait anger-out on acute pain sensitivity

被引:14
作者
Bruehl, Stephen [1 ]
Chung, Ok Y. [1 ]
Burns, John W. [2 ]
机构
[1] Vanderbilt Univ, Sch Med, Dept Anesthesiol, Nashville, TN 37212 USA
[2] Rosalind Franklin Univ Med & Sci, Dept Psychol, N Chicago, IL USA
基金
美国国家卫生研究院;
关键词
Anger-in; Anger-out; Anger expression; Pain; Opioid; Genetic A118G; Anger management style; Anger suppression;
D O I
10.1016/j.pain.2008.05.014
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Both trait anger-in (managing anger through suppression) and anger-out (managing anger through direct expression) are related to pain responsiveness, but only anger-out effects involve opioid mehcanisms. Preliminary work suggested that the effects of anger-out on postoperative analgesic requirements were moderated by the A118G single nucleotide polymorphism of the mu opioid receptor gene. This study further explored these potential genotype x phenotype interactions as they impact acute pain sensitivity. Genetic samples and measures of anger-in and anger-out were obtained in 87 subjects (from three studies) who participated in controlled laboratory acute pain tasks (ischemic, finger pressure, thermal). McGill Pain Questionnaire (MPQ) Sensory and Affective ratings for each pain task were standardized within studies, aggregated across pain tasks, and combined for analyses. Significant anger-out x A118G interactions were observed (p's < .05). Simple effects testss for both pain measures revealed that whereas anger-out was nonsignificantly hyperalgesic in subjects homozygous for the wild-type allele, anger-out was significantly hypoalgesic in those with the variant G allele (p's < .05). For the MPQ-Affective measure, this interaction arose both from low pain sensitivity in high anger-out subjects with the G allele and heightened pain sensitivity in low anger-out subjects with the G allele relative to responses in homozygous wild-type subjectss. No genetic moderation was observed for anger-in, although significant main effects on MPQ-Affective ratings were noted (p < .005). Anger-in main effects were due to overlap with negative affect, but anger-out-A118G interactions were not, suggesting unique effects of expressive anger regulation. Results support opioid-related geno-type x phnotype interactions were involving trait anger-out. (C) 2008 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:406 / 415
页数:10
相关论文
共 44 条
[1]  
Aiken L. S., 1991, Multiple Regression: Testing and Interpreting Interactions
[2]   THE MODERATOR MEDIATOR VARIABLE DISTINCTION IN SOCIAL PSYCHOLOGICAL-RESEARCH - CONCEPTUAL, STRATEGIC, AND STATISTICAL CONSIDERATIONS [J].
BARON, RM ;
KENNY, DA .
JOURNAL OF PERSONALITY AND SOCIAL PSYCHOLOGY, 1986, 51 (06) :1173-1182
[3]   AN INVENTORY FOR MEASURING DEPRESSION [J].
BECK, AT ;
ERBAUGH, J ;
WARD, CH ;
MOCK, J ;
MENDELSOHN, M .
ARCHIVES OF GENERAL PSYCHIATRY, 1961, 4 (06) :561-&
[4]   INABILITY TO EXPRESS INTENSE AFFECT - A COMMON LINK BETWEEN DEPRESSION AND PAIN [J].
BEUTLER, LE ;
ENGLE, D ;
OROBEUTLER, ME ;
DALDRUP, R ;
MEREDITH, K .
JOURNAL OF CONSULTING AND CLINICAL PSYCHOLOGY, 1986, 54 (06) :752-759
[5]   Single-nucleotide polymorphism in the human mu opioid receptor gene alters β-endorphin binding and activity:: Possible implications for opiate addiction [J].
Bond, C ;
LaForge, KS ;
Tian, MT ;
Melia, D ;
Zhang, SW ;
Borg, L ;
Gong, JH ;
Schluger, J ;
Strong, JA ;
Leal, SM ;
Tischfield, JA ;
Kreek, MJ ;
Yu, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) :9608-9613
[6]   Anger and pain sensitivity in chronic low back pain patients and pain-free controls: the role of endogenous opioids [J].
Bruehl, S ;
Burns, JW ;
Chung, OY ;
Ward, P ;
Johnson, B .
PAIN, 2002, 99 (1-2) :223-233
[7]   Anger regulation style, postoperative pain, and relationship to the A118G mu opioid receptor gene polymorphism: A preliminary study [J].
Bruehl, S ;
Chung, OY ;
Donahue, BS ;
Burns, JW .
JOURNAL OF BEHAVIORAL MEDICINE, 2006, 29 (02) :161-169
[8]   The association between anger expression and chronic pain intensity: evidence for partial mediation by endogenous opioid dysfunction [J].
Bruehl, S ;
Chung, OY ;
Burns, JW ;
Biridepalli, S .
PAIN, 2003, 106 (03) :317-324
[9]   Trait anger expressiveness and pain-induced beta-endorphin release: Support for the oploid dysfunction hypothesis [J].
Bruehl, Stephen ;
Chung, Ok Y. ;
Burns, John W. ;
Diedrich, Laura .
PAIN, 2007, 130 (03) :208-215
[10]   Anger management style and endogenous opioid function: Is gender a moderator? [J].
Bruehl, Stephen ;
al'Absi, Mustafa ;
France, Christopher R. ;
France, Janis ;
Harju, Angie ;
Burns, John W. ;
Chung, Ok Y. .
JOURNAL OF BEHAVIORAL MEDICINE, 2007, 30 (03) :209-219