TY - JOUR
T1 - Association of aberrant brain network dynamics with gut microbial composition uncovers disrupted brain–gut–microbiome interactions in irritable bowel syndrome
T2 - Preliminary findings
AU - Yang, Lin
AU - Liu, Guangyao
AU - Li, Shan
AU - Yao, Chaofan
AU - Zhao, Ziyang
AU - Chen, Nan
AU - Zhang, Pengfei
AU - Shang, Yingying
AU - Wang, Yin
AU - Zhang, Dekui
AU - Tian, Xiaozhu
AU - Zhang, Jing
AU - Yao, Zhijun
AU - Hu, Bin
N1 - Publisher Copyright:
© 2023 European Academy of Neurology.
PY - 2023/11
Y1 - 2023/11
N2 - Background and purpose: Growing evidence suggests that abnormalities in brain–gut–microbiome (BGM) interactions are involved in the pathogenesis of irritable bowel syndrome (IBS). Our study aimed to explore alterations in dynamic functional connectivity (DFC), the gut microbiome and the bidirectional interaction in the BGM. Methods: Resting-state functional magnetic resonance imaging (rs-fMRI), fecal samples and clinical chacteristics were collected from 33 IBS patients and 32 healthy controls. We performed a systematic DFC analysis on rs-fMRI. The gut microbiome was analyzed by 16S rRNA gene sequencing. Associations between DFC characteristics and microbial alterations were explored. Results: In the DFC analysis, four dynamic functional states were identified. IBS patients exhibited increased mean dwell and fraction time in State 4, and reduced transitions from State 3 to State 1. Aberrant temporal properties in State 4 were only evident when choosing a short window (36 s or 44 s). Decreased functional connectivity (FC) variability was found in State 1 and State 3 in IBS patients, two of which (independent component [IC]51-IC91, IC46-IC11) showed significant correlations with clinical characteristics. Additionally, we identified nine significantly differential abundances in microbial composition. We also found that IBS-related microbiota were associated with aberrant FC variability, although these exploratory results were obtained at an uncorrected threshold of significance. Conclusions: Although future studies are needed to confirm our results, the findings not only provide a new insight into the dysconnectivity hypothesis in IBS from a dynamic perspective, but also establish a possible link between DFC and the gut microbiome, which lays the foundation for future research on disrupted BGM interactions.
AB - Background and purpose: Growing evidence suggests that abnormalities in brain–gut–microbiome (BGM) interactions are involved in the pathogenesis of irritable bowel syndrome (IBS). Our study aimed to explore alterations in dynamic functional connectivity (DFC), the gut microbiome and the bidirectional interaction in the BGM. Methods: Resting-state functional magnetic resonance imaging (rs-fMRI), fecal samples and clinical chacteristics were collected from 33 IBS patients and 32 healthy controls. We performed a systematic DFC analysis on rs-fMRI. The gut microbiome was analyzed by 16S rRNA gene sequencing. Associations between DFC characteristics and microbial alterations were explored. Results: In the DFC analysis, four dynamic functional states were identified. IBS patients exhibited increased mean dwell and fraction time in State 4, and reduced transitions from State 3 to State 1. Aberrant temporal properties in State 4 were only evident when choosing a short window (36 s or 44 s). Decreased functional connectivity (FC) variability was found in State 1 and State 3 in IBS patients, two of which (independent component [IC]51-IC91, IC46-IC11) showed significant correlations with clinical characteristics. Additionally, we identified nine significantly differential abundances in microbial composition. We also found that IBS-related microbiota were associated with aberrant FC variability, although these exploratory results were obtained at an uncorrected threshold of significance. Conclusions: Although future studies are needed to confirm our results, the findings not only provide a new insight into the dysconnectivity hypothesis in IBS from a dynamic perspective, but also establish a possible link between DFC and the gut microbiome, which lays the foundation for future research on disrupted BGM interactions.
KW - brain–gut–microbiome axis
KW - dynamic functional connectivity
KW - gut microbiome
KW - irritable bowel syndrome
KW - resting-state functional MRI
UR - http://www.scopus.com/inward/record.url?scp=85151959491&partnerID=8YFLogxK
U2 - 10.1111/ene.15776
DO - 10.1111/ene.15776
M3 - Article
C2 - 36905309
AN - SCOPUS:85151959491
SN - 1351-5101
VL - 30
SP - 3529
EP - 3539
JO - European Journal of Neurology
JF - European Journal of Neurology
IS - 11
ER -