Department of Psychology, Laboratory of Neurogenetics, University of Bonn, Bonn, Germany.
Department of Psychology, Laboratory of Neurogenetics, University of Bonn, Bonn, Germany,
Neuropsychobiology. 2020;79(2):150-160. doi: 10.1159/000504227. Epub 2019 Dec 5.
The hypothalamus-pituitary-adrenal (HPA) axis, the biological substrate of stress reactivity, and related genetic variations play a crucial role in the initiation and maintenance of drug addiction. On the behavioral level, substance abusers are characterized by impulsivity and the inability to pursue long-term goals. The neural substrate of these behaviors is assumed to be related to the ventromedial prefrontal cortex (VMPFC). One of the most established paradigms to assess VMPFC deficiency is the IOWA gambling task (IGT).
The aim of this study was to investigate the interplay between the HPA axis-related genetic variation on corticotropin-releasing hormone (CRH; secreted from the hypothalamus and constituting the starting point of the HPA axis) gene and opioid addiction, with respect to IGT performance. There is some evidence that stress and pathological HPA axis hyperactivity, in the same way as drug addiction, is related to a poorer IGT performance.
In total, 138 long-term opioid addicts (mean age 38.63 years [SD 9.15]) and 160 healthy controls (mean age 22.57 years [SD 5.86]) performed the IGT and were genotyped for 6 SNPs covering the CRH gene and adjacent regions (rs3176921, rs6999780, rs7816410, rs1870393, rs1814583, and rs11996294). The first 5 of these 6 SNPs build a haplotype block spanning 15 kb on the CRH gene.
We found a significant group difference in the total IGT score, with higher scores in controls than in opioids. Most interestingly, there was a 3-way interaction, group × haplotype × block. Carriers homozygous for the TGTAA-haplotype differed in IGT performance dependent on group. In the control group, carriers homozygous for the TGTAA-haplotype showed a linear learning curve across blocks of trials, which was not observed in participants without this homozygosity. There were diametric effects in opioid addicts. Controlling for age and gender did not change the findings.
This study provides genetic evidence for the interplay between stress, decision-making, and opioid addiction.
下丘脑-垂体-肾上腺(HPA)轴是应激反应的生物学基础,相关的遗传变异在药物成瘾的发生和维持中起着关键作用。在行为层面上,物质滥用者的特点是冲动和无法追求长期目标。这些行为的神经基础被认为与腹内侧前额叶皮层(VMPFC)有关。评估 VMPFC 缺陷的最成熟的范式之一是爱荷华赌博任务(IGT)。
本研究旨在探讨 HPA 轴相关的促肾上腺皮质激素释放激素(CRH;从下丘脑分泌,构成 HPA 轴的起点)基因的遗传变异与阿片类药物成瘾之间的相互作用,以及与 IGT 表现的关系。有证据表明,应激和病理性 HPA 轴过度活跃,与药物成瘾一样,与较差的 IGT 表现有关。
共有 138 名长期阿片类药物成瘾者(平均年龄 38.63 岁[标准差 9.15])和 160 名健康对照者(平均年龄 22.57 岁[标准差 5.86])完成了 IGT,并对覆盖 CRH 基因和相邻区域的 6 个 SNP(rs3176921、rs6999780、rs7816410、rs1870393、rs1814583 和 rs11996294)进行了基因分型。这 6 个 SNP 中的前 5 个构成了跨越 CRH 基因 15kb 的单倍型块。
我们发现总 IGT 评分存在显著的组间差异,对照组的得分高于阿片类药物组。最有趣的是,存在一个 3 路相互作用,即组×单倍型×块。在 TGTAA-单倍型纯合子中,TGTAA-单倍型携带者的 IGT 表现因组而异。在对照组中,TGTAA-单倍型携带者在整个试验块中表现出线性学习曲线,而没有这种纯合性的参与者则没有表现出这种曲线。阿片类药物成瘾者则出现了相反的效果。控制年龄和性别并不能改变这些发现。
本研究提供了遗传证据,证明了应激、决策和阿片类药物成瘾之间的相互作用。