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Combined analysis of circulating β-endorphin with gene polymorphisms in OPRM1, CACNAD2 and ABCB1 reveals correlation with pain, opioid sensitivity and opioid-related side effects.
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The treatment of moderate to severe pain is largely dependent on the use of opioids [1]. Opioids have a narrow therapeutic index with wide variations in individual response [2]. Significant individual differences in sensitivity to these drugs can impair effective pain treatment and increase side effects. It is assumed that individual differences in opioid sensitivity may be due in part to genetic differences in the molecular elements involved in the pharmacokinetics and pharmacodynamics of opioids. Thus, genetic variability such as polymorphisms in the genes coding for opioid-metabolizing enzymes, transporter proteins, and the μ-opioid receptor could partly explain the observed inter-individual variations in response to opioids [3-5].