Stony Brook University Department of Psychology, Stony Brook, NY, United States of America.
Stony Brook University Department of Psychology, Stony Brook, NY, United States of America.
Schizophr Res. 2021 Dec;238:161-169. doi: 10.1016/j.schres.2021.10.006. Epub 2021 Oct 22.
Mismatch negativity (MMN) amplitude is reliably reduced in psychotic disorders. While several studies have examined this effect in first-degree relatives of individuals with schizophrenia, few have sought to quantify deficits in relatives of individuals with other psychotic disorders. While some conclude that, compared to healthy subjects, first-degree relatives of schizophrenia show reduced MMN, others contradict this finding. Furthermore, though MMN is often shown to be associated with cognitive impairments and clinical symptoms in psychotic disorders, to our knowledge no studies have sought to fully examine these relationships in studies of first-degree relatives. The present study sought to clarify the extent of MMN amplitude reductions in a large sample of siblings of individuals with diverse psychotic disorders (n = 67), compared to probands with psychosis (n = 221) and never psychotic comparison subjects (n = 251). We further examined associations of MMN amplitude with cognition and schizotypal symptoms across these groups. We found that MMN amplitude was intact in siblings compared to probands. MMN amplitude was associated with cognition and schizotypal symptoms dimensionally across levels of familial risk. The present results imply that MMN reductions do not reflect genetic risk for psychotic disorders per se, and instead emerge as a result of, or in conjunction with, clinical features associated with psychosis. Such findings carry important implications for the utility of MMN amplitude as an indicator of inherited risk, and suggest that this component may be best conceptualized as an endophenotype for clinical symptoms and cognitive impairments, rather than risk for psychosis per se.
失匹配负波(MMN)幅度在精神病障碍中可靠降低。虽然有几项研究检查了精神分裂症患者一级亲属的这种影响,但很少有研究试图量化其他精神病障碍患者一级亲属的缺陷。虽然一些研究得出结论,与健康受试者相比,精神分裂症患者的一级亲属的 MMN 减少,但其他研究结果则与此相反。此外,尽管 MMN 通常与精神病障碍中的认知障碍和临床症状相关,但据我们所知,在对一级亲属的研究中,没有研究试图全面检查这些关系。本研究旨在阐明在患有各种精神病障碍的个体的兄弟姐妹(n=67)的大样本中,与精神病患者(n=221)和从未出现精神病的对照受试者(n=251)相比,MMN 幅度降低的程度。我们进一步检查了这些组中 MMN 幅度与认知和精神分裂症样症状的关联。我们发现,与患者相比,兄弟姐妹的 MMN 幅度正常。MMN 幅度与认知和精神分裂症样症状维度相关,与家族风险水平相关。目前的结果表明,MMN 减少并不反映精神病障碍的遗传风险本身,而是作为与精神病相关的临床特征的结果或与其同时出现。这些发现对 MMN 幅度作为遗传风险的指标的实用性具有重要意义,并表明该成分最好被概念化为临床症状和认知障碍的内表型,而不是精神病本身的风险。