Yang Zhiyong, Wang Guanghui, Luo Nan, Tsang Chi Kwan, Huang Li'an
Clinical Neuroscience Institute, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Department of Neurology, The First Clinical Medical School of Jinan University, Guangzhou, China.
Front Neurol. 2022 Aug 5;13:937501. doi: 10.3389/fneur.2022.937501. eCollection 2022.
Acute ischemic stroke (AIS) is a primary cause of mortality and morbidity worldwide. Currently, no clinically approved immune intervention is available for AIS treatment, partly due to the lack of relevant patient classification based on the peripheral immunity status of patients with AIS. In this study, we adopted the consensus clustering approach to classify patients with AIS into molecular subgroups based on the transcriptomic profiles of peripheral blood, and we identified three distinct AIS molecular subgroups and 8 modules in each subgroup by the weighted gene co-expression network analysis. Remarkably, the pre-ranked gene set enrichment analysis revealed that the co-expression modules with subgroup I-specific signature genes significantly overlapped with the differentially expressed genes in AIS patients with hemorrhagic transformation (HT). With respect to subgroup II, exclusively male patients with decreased proteasome activity were identified. Intriguingly, the majority of subgroup III was composed of female patients who showed a comparatively lower level of AIS-induced immunosuppression (AIIS). In addition, we discovered a non-linear relationship between female age and subgroup-specific gene expression, suggesting a gender- and age-dependent alteration of peripheral immunity. Taken together, our novel AIS classification approach could facilitate immunomodulatory therapies, including the administration of gender-specific therapeutics, and attenuation of the risk of HT and AIIS after ischemic stroke.
急性缺血性卒中(AIS)是全球范围内导致死亡和发病的主要原因。目前,尚无临床批准的免疫干预措施可用于AIS治疗,部分原因是缺乏基于AIS患者外周免疫状态的相关患者分类。在本研究中,我们采用共识聚类方法,根据外周血转录组谱将AIS患者分类为分子亚组,并通过加权基因共表达网络分析在每个亚组中鉴定出三个不同的AIS分子亚组和8个模块。值得注意的是,预排序基因集富集分析显示,具有亚组I特异性特征基因的共表达模块与发生出血性转化(HT)的AIS患者中的差异表达基因显著重叠。对于亚组II,鉴定出蛋白酶体活性降低的男性患者。有趣的是,亚组III主要由女性患者组成,这些女性患者表现出相对较低水平的AIS诱导的免疫抑制(AIIS)。此外,我们发现女性年龄与亚组特异性基因表达之间存在非线性关系,表明外周免疫存在性别和年龄依赖性改变。综上所述,我们新颖的AIS分类方法可促进免疫调节治疗,包括给予性别特异性治疗药物,以及降低缺血性卒中后HT和AIIS的风险。