Lledós Miquel, Prats-Sánchez Luís, Muiño Elena, Cullell Natalia, Llucià-Carol Laia, Cárcel-Márquez Jara, Gallego-Fabrega Cristina, Martín-Campos Jesús M, Marín Rebeca, Aguilera-Simón Ana, Guasch-Jiménez Marina, Ezcurra-Díaz Garbiñe, Camps-Renom Pol, Del Mar Freijo María, Martí-Fàbregas Joan, Fernández-Cadenas Israel
Stroke Pharmacogenomics and Genetics Laboratory, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Genetics, Microbiology and Statistics Department, Universitat de Barcelona, Barcelona, Spain.
Eur J Neurol. 2025 Jul;32(7):e70265. doi: 10.1111/ene.70265.
Functional recovery from ischemic stroke (IS), the main cause of adult disability worldwide, is influenced by many factors, and a portion of interindividual variability remains unexplained.
Observational study in a tertiary stroke centre of patients with IS analyzed using shotgun metagenomic sequencing (January 2020-March 2022). Functional outcomes were assessed according to modified Rankin Scale (mRS) scores 3-months post-IS, considering 0-2 favorable and 3-6 unfavorable. The causal relationship between several bacteria and post-IS outcomes was explored via two-sample Mendelian randomization (MR) analyses using Genome-Wide Association Analysis (GWAS) summary statistics.
Comparing 128 patients with favorable and unfavorable post-IS functional outcomes, β-diversity analysis showed a separation in microbial structure, and α-diversity measures revealed greater bacterial richness in the favorable outcomes group. Taxonomic profiling of the samples showed that a greater abundance of pathogenic bacteria (e.g., Pseudomonas, Finegoldia, Porphyromonas) was associated with an unfavorable outcome. Functional profiling of the samples revealed differences in the ethylbenzene degradation pathway and in 16S rRNA (uracil1498-N3)-methyltransferase. MR confirmed increased pyruvate levels to be causally associated with post-IS favorable outcomes (β = -0.50, 95% CI: -0.91, -0.10).
Our study points to gut microbiota differences in patients with unfavorable versus favorable 3-month post-IS outcomes. Patients with unfavorable outcomes presented gut microbiota dysbiosis and alterations in multiple metabolic pathways.
This study was registered on 3 October 2021 with https://clinicaltrials.gov. Access number: NCT04795687.
缺血性中风(IS)是全球成人残疾的主要原因,其功能恢复受多种因素影响,部分个体间差异仍无法解释。
在一家三级中风中心对IS患者进行观察性研究,采用鸟枪法宏基因组测序分析(2020年1月至2022年3月)。根据IS后3个月的改良Rankin量表(mRS)评分评估功能结局,将0 - 2分视为良好,3 - 6分视为不良。使用全基因组关联分析(GWAS)汇总统计数据,通过两样本孟德尔随机化(MR)分析探索几种细菌与IS后结局之间的因果关系。
比较128例IS后功能结局良好和不良的患者,β多样性分析显示微生物结构存在差异,α多样性测量显示良好结局组的细菌丰富度更高。样本的分类学分析表明,大量致病细菌(如假单胞菌、纤细杆菌、卟啉单胞菌)与不良结局相关。样本的功能分析揭示了乙苯降解途径和16S rRNA(尿嘧啶1498 - N3)甲基转移酶的差异。MR证实丙酮酸水平升高与IS后良好结局存在因果关系(β = -0.50,95%CI:-0.91,-0.10)。
我们的研究指出了IS后3个月结局不良与良好的患者之间肠道微生物群的差异。结局不良的患者存在肠道微生物群失调和多种代谢途径的改变。
本研究于2021年10月3日在https://clinicaltrials.gov注册。注册号:NCT04795687。