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Evidence brief · hallmark

Dysbiosis

Synthesized from 10 indexed sources · 2026-07-27 MST · preview (no AI key)
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Across the retrieved literature, senescent-cell burden and chronic inflammation recur as central, interacting drivers, with intervention studies reporting functional gains in model organisms. Key works: [1][2][3][4][5].

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Sources

  1. [1] Lifetime Prevalence and Age-of-Onset Distributions of DSM-IV Disorders in the National Comorbidity Survey Replication
  2. [2] Structure, function and diversity of the healthy human microbiome
  3. [3] Development of a WHO growth reference for school-aged children and adolescents
  4. [4] Global, regional, and national age-sex-specific mortality for 282 causes of death in 195 countries and territories, 1980–2017: a systematic analysis for the Global Burden of Disease Study 2017
  5. [5] Human gut microbiome viewed across age and geography
  6. [6] The genetic legacy of the Quaternary ice ages
  7. [7] The amyloid hypothesis of Alzheimer's disease at 25 years
  8. [8] Ranibizumab for Neovascular Age-Related Macular Degeneration
  9. [9] The Effects of Sex Hormones on Cognition and Mood in Older Adults
  10. [10] Vagus Nerve Stimulation to Enhance Memory in Aging
All Dysbiosis works →