Department of Psychiatry, University of Muenster, Muenster, Germany.
Mol Psychiatry. 2011 Sep;16(9):938-48. doi: 10.1038/mp.2010.81. Epub 2010 Jul 6.
Animal studies have suggested neuropeptide S (NPS) and its receptor (NPSR) to be involved in the pathogenesis of anxiety-related behavior. In this study, a multilevel approach was applied to further elucidate the role of NPS in the etiology of human anxiety. The functional NPSR A/T (Asn¹⁰⁷Ile) variant (rs324981) was investigated for association with (1) panic disorder with and without agoraphobia in two large, independent case-control studies, (2) dimensional anxiety traits, (3) autonomic arousal level during a behavioral avoidance test and (4) brain activation correlates of anxiety-related emotional processing in panic disorder. The more active NPSR rs324981 T allele was found to be associated with panic disorder in the female subgroup of patients in both samples as well as in a meta-analytic approach. The T risk allele was further related to elevated anxiety sensitivity, increased heart rate and higher symptom reports during a behavioral avoidance test as well as decreased activity in the dorsolateral prefrontal, lateral orbitofrontal and anterior cingulate cortex during processing of fearful faces in patients with panic disorder. The present results provide converging evidence for a female-dominant role of NPSR gene variation in panic disorder potentially through heightened autonomic arousal and distorted processing of anxiety-relevant emotional stimuli.
动物研究表明神经肽 S(NPS)及其受体(NPSR)参与了焦虑相关行为的发病机制。在这项研究中,采用了多层次的方法来进一步阐明 NPS 在人类焦虑症病因中的作用。研究了功能性 NPSR A/T(Asn¹⁰⁷Ile)变体(rs324981)与(1)伴或不伴广场恐怖症的惊恐障碍、(2)多维焦虑特征、(3)行为回避测试期间的自主唤醒水平以及(4)惊恐障碍相关的焦虑情绪处理的大脑激活相关性之间的关联。发现更活跃的 NPSR rs324981 T 等位基因与两个样本中患者的女性亚组中的惊恐障碍有关,并且在荟萃分析中也是如此。T 风险等位基因与焦虑敏感性升高、心率增加以及行为回避测试期间的症状报告增加有关,并且与惊恐障碍患者处理恐惧面孔时背外侧前额叶、外侧眶额皮质和前扣带皮质的活动减少有关。这些结果提供了一致的证据,表明 NPSR 基因变异在惊恐障碍中可能具有女性优势,其作用机制可能是通过增强自主唤醒和扭曲处理与焦虑相关的情绪刺激。