Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden; Center for Molecular Medicine, Karolinska University Hospital Solna, Stockholm, Sweden.
Centre for Translational Microbiome Research (CTMR), Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.
Brain Behav Immun. 2024 Mar;117:298-309. doi: 10.1016/j.bbi.2024.01.218. Epub 2024 Jan 26.
While an association between the gut microbiome and schizophrenia spectrum disorders (SSD) has been suggested, the existing evidence is still inconclusive. To this end, we analyzed bacteria and bacterial genes in feces from 52 young adult SSD patients and 52 controls using fecal shotgun metagenomic sequencing. Compared to controls, young SSD patients were found to have significantly lower α-diversity and different β-diversity both regarding bacterial species (i.e., taxonomic diversity) and bacterial genes (i.e., functional diversity). Furthermore, the α-diversity measures 'Pielou's evenness' and 'Shannon' were significantly higher for both bacterial species, bacterial genes encoding enzymes and gut brain modules in young SSD patients on antipsychotic treatment (young SSD not on antipsychotics=9 patients, young SSD on antipsychotics=43 patients). We also applied machine learning classifiers to distinguish between young SSD patients and healthy controls based on their gut microbiome. Results showed that taxonomic and functional data classified young SSD individuals with an accuracy of ≥ 70% and with an area under the receiver operating characteristic curve (AUROC) of ≥ 0.75. Differential abundance analysis on the most important features in the classifier models revealed that most of the species with higher abundance in young SSD patients had their natural habitat in the oral cavity. In addition, many of the modules with higher abundance in young SSD patients were amino acid biosynthesis modules. Moreover, the abundances of gut-brain modules of butyrate synthesis and acetate degradation were lower in the SSD patients compared to controls. Collectively, our findings continue to support the presence of gut microbiome alterations in SSD and provide support for the use of machine learning algorithms to distinguish patients from controls based on gut microbiome profiles.
虽然肠道微生物群与精神分裂症谱系障碍(SSD)之间存在关联,但现有证据仍不确定。为此,我们使用粪便宏基因组测序分析了 52 名年轻 SSD 患者和 52 名对照的粪便中的细菌和细菌基因。与对照组相比,年轻 SSD 患者的细菌种类(即分类多样性)和细菌基因(即功能多样性)的 α 多样性和 β 多样性均显著降低。此外,对于接受抗精神病药物治疗的年轻 SSD 患者(未接受抗精神病药物治疗的年轻 SSD=9 例,接受抗精神病药物治疗的年轻 SSD=43 例),细菌种类、编码酶的细菌基因和肠道-大脑模块的 α 多样性测量值“Pielou 均匀度”和“Shannon”显著更高。我们还应用机器学习分类器基于肠道微生物组来区分年轻 SSD 患者和健康对照。结果表明,基于分类和功能数据,年轻 SSD 患者的分类准确率≥70%,接受者操作特征曲线下的面积(AUROC)≥0.75。分类器模型中最重要特征的差异丰度分析表明,年轻 SSD 患者中丰度较高的大多数物种的自然栖息地在口腔中。此外,年轻 SSD 患者中丰度较高的许多模块是氨基酸生物合成模块。此外,与对照组相比,SSD 患者的丁酸合成和乙酸降解肠道-大脑模块的丰度较低。总之,我们的研究结果继续支持 SSD 中存在肠道微生物群改变,并为使用机器学习算法根据肠道微生物组谱区分患者和对照提供了支持。