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Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies

BACKGROUND: The early life stage is critical for the gut microbiota establishment and development. We aimed to investigate the lifelong impact of famine exposure during early life on the adult gut microbial ecosystem and examine the association of famine-induced disturbance in gut microbiota with ty...

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Autores principales: Gou, Wanglong, Wang, Huijun, Tang, Xin-yi, He, Yan, Su, Chang, Zhang, Jiguo, Sun, Ting-yu, Jiang, Zengliang, Miao, Zelei, Fu, Yuanqing, Zhao, Hui, Chen, Yu-ming, Zhang, Bing, Zhou, Hongwei, Zheng, Ju-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619253/
https://www.ncbi.nlm.nih.gov/pubmed/37907866
http://dx.doi.org/10.1186/s12916-023-03123-y
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author Gou, Wanglong
Wang, Huijun
Tang, Xin-yi
He, Yan
Su, Chang
Zhang, Jiguo
Sun, Ting-yu
Jiang, Zengliang
Miao, Zelei
Fu, Yuanqing
Zhao, Hui
Chen, Yu-ming
Zhang, Bing
Zhou, Hongwei
Zheng, Ju-Sheng
author_facet Gou, Wanglong
Wang, Huijun
Tang, Xin-yi
He, Yan
Su, Chang
Zhang, Jiguo
Sun, Ting-yu
Jiang, Zengliang
Miao, Zelei
Fu, Yuanqing
Zhao, Hui
Chen, Yu-ming
Zhang, Bing
Zhou, Hongwei
Zheng, Ju-Sheng
author_sort Gou, Wanglong
collection PubMed
description BACKGROUND: The early life stage is critical for the gut microbiota establishment and development. We aimed to investigate the lifelong impact of famine exposure during early life on the adult gut microbial ecosystem and examine the association of famine-induced disturbance in gut microbiota with type 2 diabetes. METHODS: We profiled the gut microbial composition among 11,513 adults (18–97 years) from three independent cohorts and examined the association of famine exposure during early life with alterations of adult gut microbial diversity and composition. We performed co-abundance network analyses to identify keystone taxa in the three cohorts and constructed an index with the shared keystone taxa across the three cohorts. Among each cohort, we used linear regression to examine the association of famine exposure during early life with the keystone taxa index and assessed the correlation between the keystone taxa index and type 2 diabetes using logistic regression adjusted for potential confounders. We combined the effect estimates from the three cohorts using random-effects meta-analysis. RESULTS: Compared with the no-exposed control group (born during 1962–1964), participants who were exposed to the famine during the first 1000 days of life (born in 1959) had consistently lower gut microbial alpha diversity and alterations in the gut microbial community during adulthood across the three cohorts. Compared with the no-exposed control group, participants who were exposed to famine during the first 1000 days of life were associated with consistently lower levels of keystone taxa index in the three cohorts (pooled beta − 0.29, 95% CI − 0.43, − 0.15). Per 1-standard deviation increment in the keystone taxa index was associated with a 13% lower risk of type 2 diabetes (pooled odds ratio 0.87, 95% CI 0.80, 0.93), with consistent results across three individual cohorts. CONCLUSIONS: These findings reveal a potential role of the gut microbiota in the developmental origins of health and disease (DOHaD) hypothesis, deepening our understanding about the etiology of type 2 diabetes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-03123-y.
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spelling pubmed-106192532023-11-02 Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies Gou, Wanglong Wang, Huijun Tang, Xin-yi He, Yan Su, Chang Zhang, Jiguo Sun, Ting-yu Jiang, Zengliang Miao, Zelei Fu, Yuanqing Zhao, Hui Chen, Yu-ming Zhang, Bing Zhou, Hongwei Zheng, Ju-Sheng BMC Med Research Article BACKGROUND: The early life stage is critical for the gut microbiota establishment and development. We aimed to investigate the lifelong impact of famine exposure during early life on the adult gut microbial ecosystem and examine the association of famine-induced disturbance in gut microbiota with type 2 diabetes. METHODS: We profiled the gut microbial composition among 11,513 adults (18–97 years) from three independent cohorts and examined the association of famine exposure during early life with alterations of adult gut microbial diversity and composition. We performed co-abundance network analyses to identify keystone taxa in the three cohorts and constructed an index with the shared keystone taxa across the three cohorts. Among each cohort, we used linear regression to examine the association of famine exposure during early life with the keystone taxa index and assessed the correlation between the keystone taxa index and type 2 diabetes using logistic regression adjusted for potential confounders. We combined the effect estimates from the three cohorts using random-effects meta-analysis. RESULTS: Compared with the no-exposed control group (born during 1962–1964), participants who were exposed to the famine during the first 1000 days of life (born in 1959) had consistently lower gut microbial alpha diversity and alterations in the gut microbial community during adulthood across the three cohorts. Compared with the no-exposed control group, participants who were exposed to famine during the first 1000 days of life were associated with consistently lower levels of keystone taxa index in the three cohorts (pooled beta − 0.29, 95% CI − 0.43, − 0.15). Per 1-standard deviation increment in the keystone taxa index was associated with a 13% lower risk of type 2 diabetes (pooled odds ratio 0.87, 95% CI 0.80, 0.93), with consistent results across three individual cohorts. CONCLUSIONS: These findings reveal a potential role of the gut microbiota in the developmental origins of health and disease (DOHaD) hypothesis, deepening our understanding about the etiology of type 2 diabetes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-03123-y. BioMed Central 2023-11-01 /pmc/articles/PMC10619253/ /pubmed/37907866 http://dx.doi.org/10.1186/s12916-023-03123-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Gou, Wanglong
Wang, Huijun
Tang, Xin-yi
He, Yan
Su, Chang
Zhang, Jiguo
Sun, Ting-yu
Jiang, Zengliang
Miao, Zelei
Fu, Yuanqing
Zhao, Hui
Chen, Yu-ming
Zhang, Bing
Zhou, Hongwei
Zheng, Ju-Sheng
Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
title Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
title_full Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
title_fullStr Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
title_full_unstemmed Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
title_short Early-life exposure to the Great Chinese Famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
title_sort early-life exposure to the great chinese famine and gut microbiome disruption across adulthood for type 2 diabetes: three population-based cohort studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10619253/
https://www.ncbi.nlm.nih.gov/pubmed/37907866
http://dx.doi.org/10.1186/s12916-023-03123-y
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