Central Laboratory, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, China.
Department of Endocrinology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, 362000, China.
Mol Neurobiol. 2024 Dec;61(12):9977-9992. doi: 10.1007/s12035-023-03744-7. Epub 2023 Nov 23.
Depression is one of the complications in patients with polycystic ovary syndrome (PCOS) that leads to considerable mental health. Accumulating evidence suggests that human gut microbiomes are associated with the progression of PCOS and depression. However, whether microbiota influences depression development in PCOS patients is still uncharacterized. In this study, we employed metagenomic sequencing and transcriptome sequencing (RNA-seq) to profile the composition of the fecal microbiota and gene expression of peripheral blood mononuclear cells in depressed women with PCOS (PCOS-DP, n = 27) in comparison to mentally healthy women with PCOS (PCOS, n = 18) and compared with healthy control (HC, n = 27) and patients with major depressive disorder (MDD, n = 29). Gut microbiota assessment revealed distinct patterns in the relative abundance in the PCOS-DP compared to HC, MDD, and PCOS groups. Several gut microbes exhibited uniquely and significantly higher abundance in the PCOS-DP compared to PCOS patients, inducing EC Ruminococcus torques, Coprococcus comes, Megasphaera elsdenii, Acidaminococcus intestini, and Barnesiella viscericola. Bacteroides eggerthii was a potential gut microbial biomarker for the PCOS-DP. RNA-seq profiling identified that 35 and 37 genes were significantly elevated and downregulated in the PCOS-DP, respectively. The enhanced differential expressed genes (DEGs) in the PCOS-DP were enriched in pathways involved in signal transduction and endocrine and metabolic diseases, whereas several lipid metabolism pathways were downregulated. Intriguingly, genes correlated with the gut microbiota were found to be significantly enriched in pathways of neurodegenerative diseases and the immune system, suggesting that changes in the microbiota may have a systemic impact on the expression of neurodegenerative diseases and immune genes. Gut microbe-related DEGs of CREB3L3 and CCDC173 were possible molecular biomarkers and therapeutic targets of women with PCOS-DP. Our multi-omics data indicate shifts in the gut microbiome and host gene regulation in PCOS patients with depression, which is of possible etiological and diagnostic importance.
抑郁症是多囊卵巢综合征(PCOS)患者的并发症之一,会对其心理健康造成严重影响。越来越多的证据表明,人类肠道微生物组与 PCOS 和抑郁症的进展有关。然而,微生物群是否会影响 PCOS 患者的抑郁发展尚不清楚。在这项研究中,我们采用宏基因组测序和外周血单核细胞转录组测序(RNA-seq)技术,对患有抑郁症的多囊卵巢综合征患者(PCOS-DP,n=27)、心理健康的多囊卵巢综合征患者(PCOS,n=18)、健康对照者(HC,n=27)和患有重度抑郁症患者(MDD,n=29)的粪便微生物群组成和外周血单核细胞基因表达进行了分析。肠道微生物群评估显示,与 HC、MDD 和 PCOS 组相比,PCOS-DP 组的相对丰度存在明显差异。与 PCOS 患者相比,PCOS-DP 组中几种肠道微生物的丰度显著升高,包括 EC 瘤胃球菌、粪真杆菌、巨球形菌、双歧杆菌和内脏双歧杆菌。脆弱拟杆菌是 PCOS-DP 的潜在肠道微生物生物标志物。RNA-seq 分析鉴定出 35 个和 37 个基因在 PCOS-DP 中分别显著上调和下调。PCOS-DP 中差异表达基因(DEGs)显著富集于信号转导和内分泌代谢疾病途径,而一些脂质代谢途径被下调。有趣的是,与肠道微生物相关的基因在神经退行性疾病和免疫系统途径中显著富集,表明肠道微生物的变化可能对神经退行性疾病和免疫基因的表达产生全身性影响。CREB3L3 和 CCDC173 的肠道微生物相关 DEGs 可能是 PCOS-DP 女性的分子生物标志物和治疗靶点。我们的多组学数据表明,患有抑郁症的 PCOS 患者的肠道微生物群和宿主基因调控发生了变化,这可能具有病因学和诊断意义。