Evidence map›Paper›PMID 36991009›Full record

ArticleScientific reports2023

Mendelian randomization analyses reveal causal relationships between the human microbiome and longevity.

Xiaomin Liu, Leying Zou, Chao Nie, Youwen Qin, Xin Tong, Jian Wang, Huanming Yang, Xun Xu, Xin Jin, Liang Xiao and 5 more

Abstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Bridging the gap:Gut microbes · 2026
    Review
  2. Article
  3. Review
  4. The Great Bustard (Ecology and evolution · 2026
    Article
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  6. Article
  7. Review
  8. Article
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  10. Review
  11. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Xiaomin Liu *College of Life Sciences, University of Chinese Academy of Sciences, Beijing, 100049, China.
Leying Zou *BGI-Shenzhen, Shenzhen, 518083, China.
Chao Nie *BGI-Shenzhen, Shenzhen, 518083, China.
Youwen QinBGI-Shenzhen, Shenzhen, 518083, China.
Xin TongBGI-Shenzhen, Shenzhen, 518083, China.
Jian WangBGI-Shenzhen, Shenzhen, 518083, China.
Huanming YangBGI-Shenzhen, Shenzhen, 518083, China.
Xun XuBGI-Shenzhen, Shenzhen, 518083, China.
Xin JinBGI-Shenzhen, Shenzhen, 518083, China.
Liang XiaoBGI-Shenzhen, Shenzhen, 518083, China.
Tao ZhangBGI-Shenzhen, Shenzhen, 518083, China.
Junxia MinSchool of Medicine, The First Affiliated Hospital, Institute of Translational Medicine, Zhejiang University, Hangzhou, China. junxiamin@zju.edu.cn.
Yi ZengCenter for Healthy Aging and Development Studies, National School of Development, Raissun Institute for Advanced Studies, Peking University, Beijing, China. zengyi@nsd.pku.edu.cn.
Huijue JiaGreater Bay Area Institute of Precision Medicine (Guangzhou), Fudan University, Shanghai, China. jiahuijue@genomics.cn.
Yong HouBGI-Shenzhen, Shenzhen, 518083, China. houyong@genomics.cn.

Funding

THE RANGE OF MALE-FEMALE MORTALITY DIFFERENCESP01AG031719 · NIA · DUKE UNIVERSITY · PI CHRISTENSEN, KAARE · 2009 to 2020
$10.2M
NIA NIH HHS P01 AG031719
6 · The paper itself

Abstract

Although recent studies have revealed the association between the human microbiome especially gut microbiota and longevity, their causality remains unclear. Here, we assess the causal relationships between the human microbiome (gut and oral microbiota) and longevity, by leveraging bidirectional two-sample Mendelian randomization (MR) analyses based on genome-wide association studies (GWAS) summary statistics of the gut and oral microbiome from the 4D-SZ cohort and longevity from the CLHLS cohort. We found that some disease-protected gut microbiota such as Coriobacteriaceae and Oxalobacter as well as the probiotic Lactobacillus amylovorus were related to increased odds of longevity, whereas the other gut microbiota such as colorectal cancer pathogen Fusobacterium nucleatum, Coprococcus, Streptococcus, Lactobacillus, and Neisseria were negatively associated with longevity. The reverse MR analysis further revealed genetically longevous individuals tended to have higher abundances of Prevotella and Paraprevotella but lower abundances of Bacteroides and Fusobacterium species. Few overlaps of gut microbiota-longevity interactions were identified across different populations. We also identified abundant links between the oral microbiome and longevity. The additional analysis suggested that centenarians genetically had a lower gut microbial diversity, but no difference in oral microbiota. Our findings strongly implicate these bacteria to play a role in human longevity and underscore the relocation of commensal microbes among different body sites that would need to be monitored for long and healthy life.

Indexed as

LongevityMicrobiotaAged, 80 and overGenome-Wide Association StudyHumansLactobacillus acidophilusMendelian Randomization Analysis

Identifiers

PMID36991009
PMCPMC10052271

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.