Miyano Takuya, Mikkaichi Tsuyoshi, Nakamura Kouichi, Yoshigae Yasushi, Abernathy Kelly, Ogura Yuji, Kiyosawa Naoki
Translational Science Department II, Daiichi Sankyo Co., Ltd., 1-2-58 Hiromachi, Shinagawa, Tokyo 140-8710, Japan.
Clinical Research Department, Sirtsei Pharmaceuticals, Inc., 3000 RDU Center Drive, Suite 130, Morrisville, NC 27560, USA.
Int J Mol Sci. 2024 Apr 12;25(8):4291. doi: 10.3390/ijms25084291.
Schizophrenia is a complex and heterogenous psychiatric disorder. This study aimed to demonstrate the potential of circulating microRNAs (miRNAs) as a clinical biomarker to stratify schizophrenia patients and to enhance understandings of their heterogenous pathophysiology. We measured levels of 179 miRNA and 378 proteins in plasma samples of schizophrenia patients experiencing acute psychosis and obtained their Positive and Negative Syndrome Scale (PANSS) scores. The plasma miRNA profile revealed three subgroups of schizophrenia patients, where one subgroup tended to have higher scores of all the PANSS subscales compared to the other subgroups. The subgroup with high PANSS scores had four distinctively downregulated miRNAs, which enriched 'Immune Response' according to miRNA set enrichment analysis and were reported to negatively regulate IL-1β, IL-6, and TNFα. The same subgroup had 22 distinctively upregulated proteins, which enriched 'Cytokine-cytokine receptor interaction' according to protein set enrichment analysis, and all the mapped proteins were pro-inflammatory cytokines. Hence, the subgroup is inferred to have comparatively high inflammation within schizophrenia. In conclusion, miRNAs are a potential biomarker that reflects both disease symptoms and molecular pathophysiology, and identify a patient subgroup with high inflammation. These findings provide insights for the precision medicinal strategies for anti-inflammatory treatments in the high-inflammation subgroup of schizophrenia.
精神分裂症是一种复杂的异质性精神疾病。本研究旨在证明循环微RNA(miRNA)作为一种临床生物标志物在对精神分裂症患者进行分层以及增进对其异质性病理生理学理解方面的潜力。我们测量了处于急性精神病发作期的精神分裂症患者血浆样本中179种miRNA和378种蛋白质的水平,并获取了他们的阳性和阴性症状量表(PANSS)评分。血浆miRNA谱揭示了精神分裂症患者的三个亚组,其中一个亚组与其他亚组相比,所有PANSS分量表的得分往往更高。PANSS评分高的亚组有四种明显下调的miRNA,根据miRNA集富集分析,这些miRNA富集于“免疫反应”,并且据报道它们对白细胞介素-1β、白细胞介素-6和肿瘤坏死因子α具有负调控作用。同一亚组有22种明显上调的蛋白质,根据蛋白质集富集分析,这些蛋白质富集于“细胞因子-细胞因子受体相互作用”,并且所有映射的蛋白质都是促炎细胞因子。因此,推断该亚组在精神分裂症中具有相对较高的炎症水平。总之,miRNA是一种潜在的生物标志物,可反映疾病症状和分子病理生理学,并识别出炎症水平高的患者亚组。这些发现为精神分裂症高炎症亚组的抗炎治疗精准医学策略提供了见解。