Department of Psychiatry, National Clinical Research Center for Mental Disorders, and National Center for Mental Disorders, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, China; China National Technology Institute on Mental Disorders, Hunan Key Laboratory of Psychiatry and Mental Health, Institute of Mental Health, and Hunan Medical Center for Mental Health, Changsha, Hunan 410011, China.
Clinical Research Center for Mental Disorders, Shanghai Pudong New Area Mental Health Center, School of Medicine, Tongji University, Shanghai 200122, China; Laboratory for Molecular Mechanisms of Brain Development, Center for Brain Science (CBS), RIKEN, Wako, Saitama, Japan.
Prog Neuropsychopharmacol Biol Psychiatry. 2024 Jul 13;133:111035. doi: 10.1016/j.pnpbp.2024.111035. Epub 2024 May 23.
Patients with psychotic diseases have been reported to exhibit abnormalities in their olfactory discrimination. These alterations have also been identified in people at high genetic or clinical risk for psychosis, suggesting olfactory discrimination dysfunction may be a potential risk factor for developing psychosis. Thus, the purpose of our study is to explore the difference in olfactory discrimination ability in the prosal stage and early stage of psychosis and to explore the potential risk factor of developed psychosis.
We compared olfactory identification and cognitive function in 89 ultra-high-risk (UHR) individuals, 103 individuals with Drug-naïve first-episode schizophrenia (FES), 81 genetic high-risk (GHR) individuals, and 97 healthy controls (HC). Additionally, we compared olfactory identification and cognitive function between two groups; UHR individuals who later transitioned to psychosis (UHR-T; n = 33) and those who did not transition (UHR-NT; n = 42)). Furthermore, we analyzed the correlations between olfactory discrimination ability and cognitive function and symptoms and compared the olfactory function between men and women.
Patients with first-episode schizophrenia (FES) and those at ultra-high risk (UHR) for psychosis exhibited more significant deficits in olfactory identification than healthy controls (HC), while no differences in olfactory identification dysfunction were observed between the genetic high risk (GHR) and HC groups. Notably, individuals in the UHR group who later developed psyhchosis displayed a steeper marked decline in their baseline olfactory identification ability than that of those in the UHR group who did not develop psychosis. Cognitive dysfunction is widely observed in both the FES and UHR groups, with a distinct correlation identified between olfactory discrimination function and cognitive performance. Finally, overall, women exhibit significantly superior olfactory function than men.
In conclusion, these findings suggest that impairment of olfactory identification exists in the early stage of psychosis. Olfactory identification dysfunction may therefore be a potential marker of predicting the transition to schizophrenia.
有报道称,精神病患者的嗅觉辨别能力存在异常。这些改变也在处于精神病高遗传或临床风险的人群中被发现,这表明嗅觉辨别功能障碍可能是发展为精神病的潜在风险因素。因此,我们的研究目的是探讨精神病前驱期和早期阶段嗅觉辨别能力的差异,并探讨发展为精神病的潜在风险因素。
我们比较了 89 名超高危(UHR)个体、103 名初发未用药精神分裂症(FES)个体、81 名遗传高风险(GHR)个体和 97 名健康对照者(HC)的嗅觉识别和认知功能。此外,我们还比较了两组之间的嗅觉识别和认知功能;后来发展为精神病的 UHR 个体(UHR-T;n=33)和未发展为精神病的 UHR 个体(UHR-NT;n=42)。此外,我们分析了嗅觉辨别能力与认知功能和症状之间的相关性,并比较了男女之间的嗅觉功能。
首发精神分裂症(FES)患者和精神病超高危(UHR)患者的嗅觉识别能力较健康对照组(HC)明显下降,而遗传高风险(GHR)组与 HC 组之间嗅觉识别功能障碍无差异。值得注意的是,UHR 组中后来发展为精神病的个体的基础嗅觉识别能力下降幅度明显大于 UHR 组中未发展为精神病的个体。认知功能障碍在 FES 和 UHR 组中均广泛存在,嗅觉辨别功能与认知表现之间存在明显相关性。最后,总体而言,女性的嗅觉功能明显优于男性。
综上所述,这些发现表明嗅觉识别障碍存在于精神病的早期阶段。嗅觉识别功能障碍可能是预测向精神分裂症转化的潜在标志物。