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. Author manuscript; available in PMC: 2011 Aug 1.
Published in final edited form as: Clin Geriatr Med. 2010 Aug;26(3):371–386. doi: 10.1016/j.cger.2010.03.002

Table 1.

Aging Changes in Joint Tissues and the Contribution of Aging to the Development of OA.

Aging Change Contribution to OA
Accumulation of cells exhibiting the senescent secretory phenotype Increased cytokine and MMP production stimulates matrix degradation
Oxidative stress/damage Increased susceptibility to cell death and reduced matrix synthesis
Decreased levels of growth factors and decreased growth factor responsiveness Reduced matrix synthesis and repair
Increased AGE formation Brittle tissue with increased fatigue failure
Reduced aggrecan size and cartilage hydration and increased collagen cleavage Reduced resiliency and tensile strength
Increased matrix calcification Altered mechanical properties and potential activation of inflammatory signaling

MMP=Matrix Metalloproteinases; AGE=Advanced Glycation End-products. Reproduced with permission from Anderson, AS and Loeser, RF, Best Pract. Res. Clin. Rheumatol . 2010; 24:15-26.