Evidence map›Paper›PMID 42423536›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Frequent Sweetened Beverage Consumption Is Associated With Accelerated Biological Aging: Evidence From a Population-Based Study and Gut Microbiota Analysis.

Yuwei Shi, Xinmei Li, Yufan Hao, Qiaoyu Wu, Yuji Yu, Siyu Li, Nuo Xu, Yi-Hsuan Wu, Eunhye Lee, Chi Chang and 5 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Yuwei ShiDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Xinmei LiDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Yufan HaoDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Qiaoyu WuDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Yuji YuDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Siyu LiDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Nuo XuDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Yi-Hsuan WuStanford Prevention Research Center, Department of Medicine, Stanford School of Medicine, Stanford University, Stanford, California, USA.
Eunhye LeeStanford Prevention Research Center, Department of Medicine, Stanford School of Medicine, Stanford University, Stanford, California, USA.
Chi ChangOffice of Medical Education Research and Development, College of Medicine, Michigan State University, East Lansing, Michigan, USA.
Emily HuStanford Prevention Research Center, Department of Medicine, Stanford School of Medicine, Stanford University, Stanford, California, USA.
Ying LuDepartment of Biomedical Data Science, Stanford School of Medicine, Stanford University, Stanford, California, USA.ORCID https://orcid.org/0000-0002-7698-8962
Elizabeth DelzellStanford Prevention Research Center, Department of Medicine, Stanford School of Medicine, Stanford University, Stanford, California, USA.
Ann W HsingStanford Prevention Research Center, Department of Medicine, Stanford School of Medicine, Stanford University, Stanford, California, USA.
Shankuan ZhuDepartment of Endocrinology of the Second Affiliated Hospital of Zhejiang University School of Medicine, Chronic Disease Research Institute, School of Public Health, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.ORCID https://orcid.org/0000-0002-9509-7364

Funding

China Medical Board (CMB)Chou Fund of Zhejiang University Education Foundation 419600-11107Cyrus Tang Foundation 419600-11102
6 · The paper itself

Abstract

Although substantial evidence links sweetened beverage (SB) intake to chronic diseases, its association with biological aging and underlying mechanisms remains unclear. This population-based study included 9104 adults aged 18-80 years from the WELL-China cohort. SB consumption was assessed using a validated food frequency questionnaire. Biological age and biological age acceleration (BAacc) were estimated using the Klemera and Doubal method (KDM). After multivariable adjustment, frequent SB consumption was significantly associated with accelerated KDM-derived BAacc, compared with non-consumers (β = 0.29 years, 95% CI: 0.06-0.52). This association was stronger among participants younger than 55 years (P for interaction < 0.05). Gut microbiota was profiled using 16S rRNA gene sequencing. We identified 10 genera significantly associated with the frequent SB consumption, and 56 genera significantly associated with BAacc. Notably, five genera (Allisonella, Lactobacillus, Weissella, Lactococcus, and Bacilli_unclassified) were shared between the two analyses and enriched in both frequent SB consumers and individuals with higher BAacc. Frequent SB consumption is associated with accelerated biological aging, especially among adults younger than 55 years. Shared gut microbial signatures associated with both SB intake and BAacc suggest a potential microbiota-related pathway. These findings support reducing SB consumption as a potential strategy for promoting healthy aging.

Indexed as

AgingBeveragesGastrointestinal MicrobiomeSugar-Sweetened BeveragesAdolescentAdultAgedAged, 80 and overChinaCohort StudiesFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16SYoung AdultRNA, Ribosomal, 16Sagingbiological age accelerationgut microbiotasweetened beverage

Identifiers

PMID42423536
PMCPMC13348652

What Socratic holds

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LicenceCC BY
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Registered trials

None linked

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.