Evidence map›Paper›PMID 41922969›Full record

ArticleBMC microbiology2026

Cold environment is associated with worse outcomes in ischemic stroke patients and the underlying gut microbial mechanism.

Chanjuan Wei, Xiao Zhou, Xiaoshuang Xia, Wenjun Feng, Lin Wang, Xin Li

Abstract read
In one paragraph

Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Chanjuan WeiDepartment of Neurology, The Second Hospital of Tianjin Medical University, No.23, PingJiang Road, Tianjin, 300211, China.
Xiao ZhouDepartment of Neurology, The Second Hospital of Tianjin Medical University, No.23, PingJiang Road, Tianjin, 300211, China.
Xiaoshuang XiaDepartment of Neurology, The Second Hospital of Tianjin Medical University, No.23, PingJiang Road, Tianjin, 300211, China.
Wenjun FengDepartment of Neurology, The Second Hospital of Tianjin Medical University, No.23, PingJiang Road, Tianjin, 300211, China.
Lin WangDepartment of Geriatrics, The Second Hospital of Tianjin Medical University, No.23, PingJiang Road, Tianjin, 300211, China.
Xin LiDepartment of Neurology, The Second Hospital of Tianjin Medical University, No.23, PingJiang Road, Tianjin, 300211, China. lixinsci@126.com.

Funding

Asian Development Bank Technical Assistance Project TA-10207 PRCKey Projects of Tianjin Municipal Health Commission TJWJ2023XK007National Natural Science Foundation of China 42275197Tianjin Key Medical Discipline (Specialty) Construction Project TJYXZDXK-3-017C
6 · The paper itself

Abstract

backgroundIncreasing evidence suggests that cold environment is a potential risk factor for acute ischemic stroke (AIS) and is associated with poor prognosis, however, its underlying mechanisms remain unclear. Since gut dysbiosis and AIS are causally related and cold environment can induce changes in the gut microbiota, we wondered whether cold-season-related gut dysbiosis aggravates stroke progression.

methodsIn total, 101 patients with AIS were enrolled and divided into two groups: cold-season onset ischemic stroke (CIS) and non-cold-season onset ischemic stroke (NCIS). Gut microbiota composition was analyzed using 16 S rRNA gene sequencing, and signature taxa were identified via linear discriminant analysis effect size (LEfSe). Correlations between key microbial taxa and clinical parameters were assessed using Spearman rank analysis. To evaluate the potential causal role of gut microbiota in cold season stroke, fecal microbiota transplantation (FMT) was performed in mice, followed by middle cerebral artery occlusion (MCAO).

resultsThe composition of gut microbiota in the CIS group significantly differed from the NCIS group. The characteristic microbiota of the CIS group was distinguished by an elevated relative abundance of Escherichia-Shigella and Enterococcus, coupled with a decreased percentage of Blautia, Eubacterium_hallii_group, Subdoligranulum, Dorea, Faecalibacterium, Ruminococcus, and Collinsella. Furthermore, Escherichia-Shigella, Enterococcus, Blautia, Eubacterium_hallii_group and Faecalibacterium showed predictive value for 3-month poor prognosis in patients. Compared with mice inoculated with the NCIS gut microbiota, mice inoculated with the CIS gut microbiota showed more severe brain damage, impaired intestinal barrier function, and higher levels of inflammatory factors after the stroke model was established.

conclusionsOur study indicates that cold-season-related gut dysbiosis may be linked to stroke severity and poor prognosis in AIS patients, suggesting that modulation of gut microbiota could represent a potential avenue for therapeutic intervention.

Indexed as

BacteriaCold TemperatureDysbiosisGastrointestinal MicrobiomeIschemic StrokeStrokeAgedAnimalsFecal Microbiota TransplantationFecesFemaleHumansMaleMiceMice, Inbred C57BLMiddle AgedRNA, Ribosomal, 16SCold environmentGut microbiotaIschemic strokeMicrobiota‒gut‒brain axisPrognosis

Identifiers

PMID41922969
PMCPMC13181897

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.