Endocrine Senescence Markers are quantifiable biochemical indicators reflecting the age-related decline or dysfunction within the hormonal system, independent of chronological age. These markers include altered steroid hormone profiles, reduced sensitivity of pituitary receptors, or changes in circulating growth factors like IGF-1. Identifying these specific biomarkers allows for a more accurate assessment of biological endocrine age versus chronological age. Recognizing these shifts is key to proactive longevity strategies.
Origin
The term fuses endocrinology with the biology of aging, where specific molecular signatures are used to gauge systemic decline. “Markers” implies measurable substances used for diagnostic or prognostic purposes within the hormonal milieu. This lexicon entry reflects the convergence of aging research and hormone replacement therapy optimization.
Mechanism
These markers function as downstream readouts of cumulative cellular stress and telomere attrition within endocrine tissues. For example, reduced DHEA-S levels or impaired TSH response often correlate with decreased tissue resilience and function across the HPA or HPT axes. Monitoring these specific molecules provides clinical leverage to identify and potentially reverse age-associated hormonal deficits.
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