4.6

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2.2

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  • ISSN 1674-8301
  • CN 32-1810/R
Zhenxiang Gong, Li Ba, Jiahui Tang, Yuan Yang, Zehui Li, Mao Liu, Chun Yang, Fengfei Ding, Min Zhang. Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study[J]. The Journal of Biomedical Research, 2023, 37(2): 125-137. DOI: 10.7555/JBR.36.20220198
Citation: Zhenxiang Gong, Li Ba, Jiahui Tang, Yuan Yang, Zehui Li, Mao Liu, Chun Yang, Fengfei Ding, Min Zhang. Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study[J]. The Journal of Biomedical Research, 2023, 37(2): 125-137. DOI: 10.7555/JBR.36.20220198

Gut microbiota links with cognitive impairment in amyotrophic lateral sclerosis: A multi-omics study

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  • Corresponding author:

    Fengfei Ding, Department of Pharmacology, School of Basic Medical Sciences; State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Shanghai Medical College, Fudan University, 130 Dong'an Road, Xuhui District, Shanghai 200032, China. Tel: +86-21-54237900, E-mail: fengfei_ding@fudan.edu.cn

    Min Zhang, Department of Neurology and Psychiatry, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1095 Jiefang Road, Qiaokou District, Wuhan, Hubei 430030, China. Tel: +86-27-83663895, E-mail: zhang_min_3464@126.com

  • Received Date: September 06, 2022
  • Revised Date: November 04, 2022
  • Accepted Date: November 21, 2022
  • Available Online: December 27, 2022
  • Recently, cognitive impairments (CI) and behavioral abnormalities in patients with amyotrophic lateral sclerosis (ALS) have been reported. However, the underlying mechanisms have been poorly understood. In the current study, we explored the role of gut microbiota in CI of ALS patients. We collected fecal samples from 35 ALS patients and 35 healthy controls. The cognitive function of the ALS patients was evaluated using the Edinburgh Cognitive and Behavioral ALS Screen. We analyzed these samples by using 16S rRNA gene sequencing as well as both untargeted and targeted (bile acids) metabolite mapping between patients with CI and patients with normal cognition (CN). We found altered gut microbial communities and a lower ratio of Firmicutes/Bacteroidetes in the CI group, compared with the CN group. In addition, the untargeted metabolite mapping revealed that 26 and 17 metabolites significantly increased and decreased, respectively, in the CI group, compared with the CN group. These metabolites were mapped to the metabolic pathways associated with bile acids. We further found that cholic acid and chenodeoxycholic acid were significantly lower in the CI group than in the CN group. In conclusion, we found that the gut microbiota and its metabolome profile differed between ALS patients with and without CI and that the altered bile acid profile in fecal samples was significantly associated with CI in ALS patients. These results need to be replicated in larger studies in the future.
  • CLC number: R744.8, Document code: A

    The authors reported no conflict of interests.

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