Background <p> Host–microbiome interactions play essential roles in the development of Alzheimer’s disease (AD), yet&#xa0;the host genetic impacts on gut microbial alterations in AD remain poorly understood.</p> Results <p>Here, we simultaneously profiled host genotype and gut microbiome in 252 Chinese individuals with varying degrees of cognitive disability. Using the latent Dirichlet allocation topic model, we identified the <i>Anaerostipes</i>-enriched enterosignature (ES-Ana) at the microbial subgroup level as significantly negatively associated with cognitive disability, which could be recapitulated in external cohorts. With the whole-genome sequencing data, we performed microbiome genome-wide association studies for the ES-Ana relative abundance. We prioritized 41 lead genetic variants and confirmed that the high ES-Ana relative abundance showed a negative correlation with the polygenic risk score of AD, indicating&#xa0;its protective effect against AD. Furthermore, we identified 174 ES-Ana-associated genes, which&#xa0;are&#xa0;enriched in AD-related biological functions and phenotypes, and exhibite pervasive underexpression in glial cells during brain aging.</p> Conclusions <p>In summary, our study reveals the complex genetic effects on the gut microbiota in AD, and provides novel evidence for the roles of the gut–brain axis in AD.</p> <p><MediaObject ID="MOESM3"> <VideoObject FileRef="MediaObjects/40168_2026_2342_MOESM3_ESM.mp4" VideoID="19Mdqa4SQc5WgL3ys2ad99"> <Caption Language="En" xml:lang="en"> <CaptionContent> <p>Video Abstract</p> </CaptionContent> </Caption> </VideoObject> </MediaObject></p>

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Impacts of host genetics on gut microbiome composition in Alzheimer’s disease

  • Jinxin Liu,
  • Jixin Cao,
  • Longhao Jia,
  • Ziquan Gan,
  • Xingzhong Zhao,
  • Anyi Yang,
  • Senying Lai,
  • Feng Chen,
  • Yucheng T. Yang,
  • Xing-Ming Zhao

摘要

Background

Host–microbiome interactions play essential roles in the development of Alzheimer’s disease (AD), yet the host genetic impacts on gut microbial alterations in AD remain poorly understood.

Results

Here, we simultaneously profiled host genotype and gut microbiome in 252 Chinese individuals with varying degrees of cognitive disability. Using the latent Dirichlet allocation topic model, we identified the Anaerostipes-enriched enterosignature (ES-Ana) at the microbial subgroup level as significantly negatively associated with cognitive disability, which could be recapitulated in external cohorts. With the whole-genome sequencing data, we performed microbiome genome-wide association studies for the ES-Ana relative abundance. We prioritized 41 lead genetic variants and confirmed that the high ES-Ana relative abundance showed a negative correlation with the polygenic risk score of AD, indicating its protective effect against AD. Furthermore, we identified 174 ES-Ana-associated genes, which are enriched in AD-related biological functions and phenotypes, and exhibite pervasive underexpression in glial cells during brain aging.

Conclusions

In summary, our study reveals the complex genetic effects on the gut microbiota in AD, and provides novel evidence for the roles of the gut–brain axis in AD.

Video Abstract