Institute for Translational Psychiatry, University of Münster, Münster 48149, Germany.
Institute for Clinical Psychology, University of Siegen, Siegen 57072, Germany.
Soc Cogn Affect Neurosci. 2024 Sep 19;19(1). doi: 10.1093/scan/nsae054.
The functional neuropeptide S receptor 1 (NPSR1) gene A/T variant (rs324981) is associated with fear processing. We investigated the impact of NPSR1 genotype on fear processing and on symptom reduction following treatment in individuals with spider phobia. A replication approach was applied [discovery sample: Münster (MS) nMS = 104; replication sample Würzburg (WZ) nWZ = 81]. Participants were genotyped for NPSR1 rs324981 [T-allele carriers (risk) versus AA homozygotes (no-risk)]. A sustained and phasic fear paradigm was applied during functional magnetic resonance imaging. A one-session virtual reality exposure treatment was conducted. Change of symptom severity from pre to post treatment and within session fear reduction were assessed. T-allele carriers in the discovery sample displayed lower anterior cingulate cortex (ACC) activation compared to AA homozygotes independent of condition. For sustained fear, this effect was replicated within a small cluster and medium effect size. No association with symptom reduction was found. Within-session fear reduction was negatively associated with ACC activation in T-allele carriers in the discovery sample. NPSR1 rs324981 genotype might be associated with fear processing in the ACC in spider phobia. Interpretation as potential risk-increasing function of the NPSR1 rs324981 T-allele via impaired top-down control of limbic structures remains speculative. Potential association with symptom reduction warrants further research.
功能性神经肽 S 受体 1(NPSR1)基因 A/T 变体(rs324981)与恐惧处理有关。我们研究了 NPSR1 基因型对蜘蛛恐惧症患者恐惧处理以及治疗后症状减轻的影响。采用了复制方法[发现样本:明斯特(MS)nMS=104;复制样本维尔茨堡(WZ)nWZ=81]。对 NPSR1 rs324981 进行基因分型[T-等位基因携带者(风险)与 AA 纯合子(无风险)]。应用功能磁共振成像进行持续和阶段性恐惧范式。进行了一次虚拟现实暴露治疗。评估了从治疗前到治疗后的症状严重程度变化以及治疗过程中的恐惧减轻。发现样本中的 T 等位基因携带者与 AA 纯合子相比,无论条件如何,其前扣带皮层(ACC)的激活都较低。对于持续恐惧,该效应在一个小簇和中等效应大小内得到了复制。与症状减轻没有关联。发现样本中 T 等位基因携带者的治疗过程中的恐惧减轻与 ACC 激活呈负相关。NPSR1 rs324981 基因型可能与蜘蛛恐惧症中 ACC 的恐惧处理有关。NPSR1 rs324981 T 等位基因通过对边缘结构的自上而下控制受损而可能增加风险的功能仍存在推测性。与症状减轻的潜在关联需要进一步研究。