Abstract

Post-stroke cognitive impairment (PSCI) is a common neuropsychiatric complication of stroke. Mounting evidence has demonstrated a connection between gut microbiota (GM) and neuropsychiatric disease. Our previous study revealed the changes in the GM in a mouse model of vascular dementia. However, the characteristic GM of PSCI remains unclear. This study aimed to characterize the GM of PSCI and explored the potential of GM as PSCI biomarkers. A total of 93 patients with ischemic stroke were enrolled in this study. The patients were divided into two groups according to their MoCA scores 3 months after stroke onset. Clinical data and biological variables were recorded. GM composition was analyzed using 16S ribosomal RNA sequencing, and the characteristic GM was identified by linear discriminant analysis Effect Size (Lefse). Our results showed that Proteobacteria was highly increased in the PSCI group compared with the post-stroke non-cognitive impairment (PSNCI) group, the similar alterations were also observed at the class, order, family, and genus levels of Proteobacteria. After age adjustments, the abundance of Firmicutes, and its members, including Clostridia, Clostridiales, Lachnospiraceae, and Lachnospiraceae_other, were significantly decreased in the age-matched PSCI group compared with the PSNCI group. Besides, the GM was closely associated with MoCA scores and the risk factors for PSCI, including higher baseline National Institute of Health Stroke Scale score, higher homocysteine (Hcy) level, higher prevalence of stroke recurrence, leukoaraiosis, and brain atrophy. The KEGG results showed the enriched module for folding, sorting and degradation (chaperones and folding catalysts) and the decreased modules related to metabolisms of cofactors and vitamins, amino acid, and lipid in PSCI patients. A significant correlation was observed between PSCI and the abundance of Enterobacteriaceae after adjustments (P = 0.035). Moreover, the receiver operating characteristic (ROC) models based on the characteristic GM and Enterobacteriaceae could distinguish PSCI patients from PSNCI patients [area under the curve (AUC) = 0.840, 0.629, respectively]. Our findings demonstrated that the characteristic GM, especially Enterobacteriaceae, might have the ability to predict PSCI in post-stroke patients, which are expected to be used as clinical biomarkers of PSCI.

Highlights

  • Ischemic stroke is a major risk factor for cognitive impairment (Vijayan and Reddy, 2016b)

  • gut microbiota (GM)’s bacterial diversity in Post-stroke cognitive impairment (PSCI) patients was similar to that of post-stroke non-cognitive impairment (PSNCI) patients, the microbial composition was distinct between the two groups

  • The abundance of Firmicutes, and its members, including Clostridia, Clostridiales, Lachnospiraceae, and Lachnospiraceae_other, were significantly decreased in the age-matched PSCI group compared with the PSNCI group

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Summary

Introduction

Ischemic stroke is a major risk factor for cognitive impairment (Vijayan and Reddy, 2016b). Stroke and cognitive impairment share similar risk factors such as hypertension and diabetes mellitus, which contribute to cognitive impairment after stroke (Sun et al, 2014). Ischemic stroke is closely correlated with cognitive impairment. Post-stroke cognitive impairment (PSCI) is a common complication of stroke. In China, the prevalence of cognitive impairment 3 months after stroke ranges from 18 to 41.8% (Tang et al, 2006; Tu et al, 2014). PSCI is associated with poor clinical outcomes such as increased hospitalization, disability, and burden of care (Crichton et al, 2016), and functional impairment is more significant in stroke survivors with cognitive impairment. Given that there is a prodromal period after stroke onset of 3 months or more before the development of PSCI (Ballard et al, 2003), it is of considerable significance to identify useful PSCI biomarkers

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