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Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging
Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging
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Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging
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Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging
Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging

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Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging
Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging
Journal Article

Sex‐Specific Aging Patterns of Gut Microbiota in Urban Chinese Adults: Guild‐Based Analysis and Implications for Healthy Aging

2025
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Overview
Gut microbial stability typically decreases with physiological aging. This decline may vary between sexes and can potentially be mitigated by adopting a healthy lifestyle. Microbial guilds, defined as functionally coherent groups of bacteria, may serve as meaningful ecological indicators of aging. This study included 2944 participants aged 51–89 years from the Shanghai Men's and Women's Health Studies. Using 16S rRNA gene sequencing and a guild‐based approach, we evaluated the associations between gut microbiota and age in 1353 relatively healthy individuals. We found that women demonstrated a decline in the Chao1 index, an increase in Pielou evenness, and a remarkable shift in Bray–Curtis distance, whereas men exhibited an increase in Bray–Curtis uniqueness. Of the 45 age‐related guilds identified, 16 (8 in men and 10 in women) were considered potential aging biomarkers (pFDR < 0.05), with Guild_6 (Bifidobacterium sp. dominated) and Guild_118 (Veillonella dispar dominated) being common to both sexes. These guilds were associated with consistent predicted functions, particularly 1,4‐dihydroxy‐2‐naphthoate biosynthesis. We estimated sex‐specific microbial age using random forest models and found that women and individuals with major chronic diseases had higher microbial ages. Prospective analysis revealed that an “old” microbial age was associated with a higher risk of type 2 diabetes (HR = 2.0, 95% CI: 1.1, 3.7). Individuals with healthier lifestyles had a 0.43‐year lower microbial age (95% CI: −0.85, −0.01). Our findings elucidate the sex‐differentiated aging patterns of gut microbiota in Chinese adults and imply the potential benefits of healthy lifestyle behaviors in slowing down microbiome aging. This study employed a guild‐based approach to identify sex‐specific age‐related gut microbiota in two large cohorts of Chinese adults. The microbial age, derived from the significant guilds identified, was higher in women and less healthy individuals, was associated with an increased risk of type 2 diabetes, and could be slowed by healthy lifestyles. These findings highlight the role of multiple major noncommunicable diseases in accelerating aging and underscore the importance of a healthy lifestyle in promoting healthy aging.