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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

Overview
Journal BMC Med
Publisher Biomed Central
Specialty General Medicine
Date 2023 Nov 1
PMID 37907866
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Abstract

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.

Citing Articles

Exposure to Chinese famine in early life and the risk of multimorbidity in adulthood.

Zhang J, Zhang L, Wu W, Zheng X BMC Public Health. 2025; 25(1):109.

PMID: 39789571 PMC: 11720307. DOI: 10.1186/s12889-025-21316-3.


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Li J, Cai H, Zhang Y, Li J, Wang D, Li H Medicine (Baltimore). 2024; 103(39):e39814.

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References
1.
Ruuskanen M, Erawijantari P, Havulinna A, Liu Y, Meric G, Tuomilehto J . Gut Microbiome Composition Is Predictive of Incident Type 2 Diabetes in a Population Cohort of 5,572 Finnish Adults. Diabetes Care. 2022; 45(4):811-818. PMC: 9016732. DOI: 10.2337/dc21-2358. View

2.
Peschel S, Muller C, von Mutius E, Boulesteix A, Depner M . NetCoMi: network construction and comparison for microbiome data in R. Brief Bioinform. 2020; 22(4). PMC: 8293835. DOI: 10.1093/bib/bbaa290. View

3.
Zmora N, Suez J, Elinav E . You are what you eat: diet, health and the gut microbiota. Nat Rev Gastroenterol Hepatol. 2018; 16(1):35-56. DOI: 10.1038/s41575-018-0061-2. View

4.
Liang S, Sin Z, Yu J, Zhao S, Xi Z, Bruzzone R . Multi-cohort analysis of depression-associated gut bacteria sheds insight on bacterial biomarkers across populations. Cell Mol Life Sci. 2022; 80(1):9. PMC: 11072413. DOI: 10.1007/s00018-022-04650-2. View

5.
Atzeni A, Bastiaanssen T, Cryan J, Tinahones F, Vioque J, Corella D . Taxonomic and Functional Fecal Microbiota Signatures Associated With Insulin Resistance in Non-Diabetic Subjects With Overweight/Obesity Within the Frame of the PREDIMED-Plus Study. Front Endocrinol (Lausanne). 2022; 13:804455. PMC: 9097279. DOI: 10.3389/fendo.2022.804455. View