Department of Psychological Sciences, University of Missouri, Columbia, Missouri.
Institute for Interdisciplinary Salivary Bioscience Research, University of California at Irvine, Irvine, California.
Alcohol Clin Exp Res. 2017 Nov;41(11):1831-1848. doi: 10.1111/acer.13491. Epub 2017 Oct 19.
Alcohol use disorder (AUD) is highly comorbid with chronic pain (CP). Evidence has suggested that neuroadaptive processes characterized by reward deficit and stress surfeit are involved in the development of AUD and pain chronification. Neurological data suggest that shared genetic architecture associated with the reward and stress systems may contribute to the comorbidity of AUD and CP. This monograph first delineates the prevailing theories of the development of AUD and pain chronification focusing on the reward and stress systems. It then provides a brief summary of relevant neurological findings followed by an evaluation of evidence documented by molecular genetic studies. Candidate gene association studies have provided some initial support for the genetic overlap between AUD and CP; however, these results must be interpreted with caution until studies with sufficient statistical power are conducted and replications obtained. Genomewide association studies have suggested a number of genes (e.g., TBX19, HTR7, and ADRA1A) that are either directly or indirectly related to the reward and stress systems in the AUD and CP literature. Evidence reviewed in this monograph suggests that shared genetic liability underlying the comorbidity between AUD and CP, if present, is likely to be complex. As the advancement in molecular genetic methods continues, future studies may show broader central nervous system involvement in AUD-CP comorbidity.
酒精使用障碍(AUD)与慢性疼痛(CP)高度共病。有证据表明,以奖励缺陷和应激过剩为特征的神经适应性过程参与了 AUD 和疼痛慢性化的发展。神经学数据表明,与奖励和应激系统相关的共同遗传结构可能导致 AUD 和 CP 的共病。本专论首先描述了 AUD 和疼痛慢性化发展的现行理论,重点关注奖励和应激系统。然后提供了相关神经学发现的简要总结,随后对分子遗传学研究记录的证据进行了评估。候选基因关联研究为 AUD 和 CP 之间的遗传重叠提供了一些初步支持;然而,在进行具有足够统计能力的研究并获得复制结果之前,必须谨慎解释这些结果。全基因组关联研究表明,一些基因(例如 TBX19、HTR7 和 ADRA1A)与 AUD 和 CP 文献中的奖励和应激系统直接或间接相关。本专论中回顾的证据表明,如果 AUD 和 CP 共病存在共同的遗传易感性,那么这种易感性很可能是复杂的。随着分子遗传学方法的不断进步,未来的研究可能会显示更广泛的中枢神经系统参与 AUD-CP 共病。