Inflammatory Cytokine Burden quantifies the total systemic load of pro-inflammatory signaling molecules, such as IL-6 and TNF-alpha, circulating within the body, often indicative of chronic, low-grade immune activation. Elevated burden is strongly associated with endocrine disruption, as inflammatory states interfere with insulin sensitivity, steroidogenesis, and thyroid hormone metabolism. We view this burden as a key driver of metabolic and hormonal resistance states.
Origin
This terminology originates from immunology and systems pathology, combining ‘Inflammatory’ to denote immune response, ‘Cytokine’ as the signaling protein class, and ‘Burden’ to express the cumulative load. In the domain of hormonal health, its relevance escalated with the understanding of immunometabolism. It represents the chronic stressor imposed by dysregulated immune signaling on the endocrine system.
Mechanism
The mechanism involves these cytokines competitively inhibiting hormone binding to receptors or directly promoting the catabolism of essential hormones within the liver. High cytokine levels often trigger the stress response, leading to chronic activation of the HPA axis and subsequent cortisol dysregulation, which suppresses sex hormone production via negative feedback. Reducing this burden is therefore a prerequisite for restoring sensitive and efficient endocrine signaling throughout the body.
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