Inflammation Burden Reduction is the deliberate lowering of chronic, subclinical systemic inflammation, often quantified by markers like high-sensitivity C-Reactive Protein (hs-CRP) and specific cytokine levels. This reduction is essential because persistent inflammation interferes with insulin signaling and disrupts healthy steroidogenesis. We aim to decrease the background noise of cellular distress.
Origin
This clinical focus stems from the recognition that chronic, non-resolving inflammation is a core component of most age-related endocrine dysfunctions. It represents a shift from treating acute inflammatory episodes to managing systemic inflammatory tone.
Mechanism
The mechanism involves modulating immune cell activation and shifting the balance of eicosanoids toward anti-inflammatory profiles, often through optimizing fatty acid intake and enhancing cellular detoxification. Furthermore, reducing visceral adiposity lessens the production of pro-inflammatory adipokines, thereby improving insulin receptor signaling and reducing the systemic load on the HPA axis.
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