Age-dependent changes in the gut microbiota and serum metabolome correlate with renal function and human aging

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  • Liang Sun
  • Zhiming Li
  • Caiyou Hu
  • Jiahong Ding
  • Qi Zhou
  • Guofang Pang
  • Zhu Wu
  • Ruiyue Yang
  • Shenghui Li
  • Jian Li
  • Jianping Cai
  • Yuzhe Sun
  • Rui Li
  • Hefu Zhen
  • Shuqin Sun
  • Jianmin Zhang
  • Mingyan Fang
  • Zhihua Chen
  • Yuan Lv
  • Qizhi Cao
  • Yanan Sun
  • Ranhui Gong
  • Zezhi Huang
  • Yong Duan
  • Hengshuo Liu
  • Jun Dong
  • Junchun Li
  • Jie Ruan
  • Haorong Lu
  • Benjin He
  • Ninghu Li
  • Tao Li
  • Wenbin Xue
  • Yan Li
  • Juan Shen
  • Fan Yang
  • Cheng Zhao
  • Qinghua Liang
  • Mingrong Zhang
  • Chen Chen
  • Huan Gong
  • Yong Hou
  • Jian Wang
  • Ying Zhang
  • Huanming Yang
  • Shida Zhu
  • Liang Xiao
  • Zhen Jin
  • Haiyun Guo
  • Peng Zhao
  • Susanne Brix
  • Xun Xu
  • Huijue Jia
  • Ze Yang
  • Chao Nie
Human aging is invariably accompanied by a decline in renal function, a process potentially exacerbated by uremic toxins originating from gut microbes. Based on a registered household Chinese Guangxi longevity cohort (n = 151), we conducted comprehensive profiling of the gut microbiota and serum metabolome of individuals from 22 to 111 years of age and validated the findings in two independent East Asian aging cohorts (Japan aging cohort n = 330, Yunnan aging cohort n = 80), identifying unique age-dependent differences in the microbiota and serum metabolome. We discovered that the influence of the gut microbiota on serum metabolites intensifies with advancing age. Furthermore, mediation analyses unveiled putative causal relationships between the gut microbiota (Escherichia coli, Odoribacter splanchnicus, and Desulfovibrio piger) and serum metabolite markers related to impaired renal function (p-cresol, N-phenylacetylglutamine, 2-oxindole, and 4-aminohippuric acid) and aging. The fecal microbiota transplantation experiment demonstrated that the feces of elderly individuals could influence markers related to impaired renal function in the serum. Our findings reveal novel links between age-dependent alterations in the gut microbiota and serum metabolite markers of impaired renal function, providing novel insights into the effects of microbiota-metabolite interplay on renal function and healthy aging.
OriginalsprogEngelsk
Artikelnummere14028
TidsskriftAging Cell
Vol/bind22
Udgave nummer12
Antal sider20
ISSN1474-9718
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
This work was financially supported by the National Scientific Foundation of P. R. China (U23A20470, 82260289, 91849132, and 81571385), the CAMS Innovation Fund for Medical Sciences (2021‐I2M‐1‐050), the National Key Research and Development Program of China (2021YFE0111800, 2023YFC3603300 and 2018YFC2000400), National High Level Hospital Clinical Research Funding (BJ‐2023‐168 and BJ‐2023‐075), the Science and Technology Innovation 2030 Major Projects (2022ZD0211600), the Priority Union Foundation of Yunnan Provincial Science and Technology Department (202001AY070001‐011), and the Beijing Hospital Nova Project (BJ‐2018‐139).

Publisher Copyright:
© 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd.

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