Opioid Pharmacogenomics Using a Twin Study Paradigm: Methods and Procedures for Determining Familial Aggregation and Heritability

被引:21
作者
Angst, Martin S. [1 ]
Phillips, Nicholas G. [1 ]
Drover, David R. [1 ]
Tingle, Martha [1 ]
Galinkin, Jeffrey L. [2 ]
Christians, Uwe [2 ]
Swan, Gary E. [3 ]
Lazzeroni, Laura C. [4 ]
Clark, J. David [1 ,5 ]
机构
[1] Stanford Univ, Sch Med, Dept Anesthesia, Stanford, CA 94305 USA
[2] Univ Colorado, Denver Hlth Sci Ctr, Childrens Hosp, Dept Anesthesiol, Aurora, CO USA
[3] SRI Int, Ctr Hlth Sci, Menlo Pk, CA 94025 USA
[4] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci & Pediat, Stanford, CA 94305 USA
[5] Vet Affairs Palo Alto Hlth Care Syst, Dept Anesthesia, Palo Alto, CA USA
关键词
pharmacogenomics; pharmacodynamics; opioid; alfentanil; twin; heritability; familial aggregation; heat pain; cold pressor pain; pain sensitivity; quantitative sensory test; analgesia; respiratory depressior; sedation; nausea; pruritus; liking; positive affective response; POSTOPERATIVE PAIN MANAGEMENT; SLEEP QUALITY INDEX; DANISH TWINS; ENVIRONMENTAL CONTRIBUTIONS; PHARMACODYNAMIC EVALUATION; RHEUMATOID-ARTHRITIS; AGE-DIFFERENCES; BLOOD-PRESSURE; BACK-PAIN; NECK PAIN;
D O I
10.1375/twin.13.5.412
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Opioids are the cornerstone medication for the treatment of moderate to severe pain. However, analgesic opioid requirements and the propensity to suffer from aversive opioid effects, including fatal respiratory depression and addiction, vary widely among patients. The factors underlying the substantial response variance remain largely unknown and need clarification for using opioids more effectively in appropriately selected patients. This ongoing study takes advantage of the twin paradigm to estimate the genetic and environmental contributions to inter-individual differences in opioid responses. Evidence of significant heritability will justify more detailed and extensive genomic studies. The enrollment target is 80 monozygotic and 45 dizygotic twin pairs who undergo a target-controlled infusion of the opioid alfentanil and saline placebo in sequential but randomized order. In a laboratory-type setting, well-defined pharmacodynamic endpoints are measured to quantify pain sensitivity, analgesic opioid effects, and aversive opioid effects including respiratory depression, sedation and reinforcing affective responses. First results obtained in 159 participants provide evidence for the feasibility and utility of this interventional study paradigm to estimate familial aggregation and heritability components of relevant drug effects. Areas highlighted in this report include recruitment strategies, required infrastructure and personnel, selection of relevant outcome measures, drug infusion algorithm minimizing pharmacokinetic variability, and considerations for optimizing data quality and quantity without hampering feasibility. Applying the twin paradigm to complex and potentially harmful studies comprehensively characterizing pharmacological response profiles is without much precedent. Methods and first results including heritability estimates for heat and cold pain sensitivity should be of interest to investigators considering similar studies.
引用
收藏
页码:412 / 425
页数:14
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