Category

Cellular and Mitochondrial Health

8 evidence-based articles

Aging is not one process. A 2023 review in Cell groups its drivers into twelve interconnected hallmarks, including genomic instability, mitochondrial dysfunction, cellular senescence, stem cell exhaustion and chronic inflammation. Each one appears with age, speeds aging when it is made worse in experiments, and offers a chance to slow aging when it is targeted.1

Two hallmarks have been studied closely. In 146 healthy adults aged 18 to 89, mitochondrial DNA, mitochondrial RNA and mitochondrial ATP production in muscle all declined with age, and ATP production tracked aerobic capacity and glucose tolerance.2 Senescent cells, which stop dividing and release inflammatory signals, build up in tissues over time; clearing them extended median lifespan in mice and slowed age-related decline in their kidneys, hearts and fat.3 That result is in mice. In people the evidence is early: a pilot trial in nine adults with diabetic kidney disease found that three days of dasatinib plus quercetin reduced senescent-cell markers in fat and skin, but it measured markers, not health outcomes.4

The articles below take each process in turn and separate what has been shown in people from what has only been shown in cells and animals.

Reading path

Read in this order: the essentials first, then the detail, then the reviews that test popular claims.

Sources

  1. 1López-Otín C, et al. "Hallmarks of aging: An expanding universe." Cell. 2023;186(2):243-278. PubMed · DOI
  2. 2Short KR, et al. "Decline in skeletal muscle mitochondrial function with aging in humans." Proc Natl Acad Sci U S A. 2005;102(15):5618-23. PubMed · DOI
  3. 3Baker DJ, et al. "Naturally occurring p16(Ink4a)-positive cells shorten healthy lifespan." Nature. 2016;530(7589):184-9. PubMed · DOI
  4. 4Hickson LJ, et al. "Senolytics decrease senescent cells in humans: Preliminary report from a clinical trial of Dasatinib plus Quercetin in individuals with diabetic kidney disease." EBioMedicine. 2019;47:446-456. PubMed · DOI
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