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DOI 10.3389/fragi.2026.1837722

Медицинская библиотека · Frontiers in aging · 2026

Physiological amplitude: a systems-level framework for adaptive capacity in aging and metabolism.

Sepczynska Grazyna

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Аннотация

BACKGROUND

Aging is characterized by progressive loss of physiological complexity, inter-system coordination, and adaptive capacity. While mitochondrial dysfunction, metabolic inflexibility, impaired stress responses, and circadian dysregulation are well established, an integrative systems-level construct linking these processes remains lacking.

OBJECTIVE

To introduce physiological amplitude as a unifying framework describing the bounded dynamic range of coordinated variability across interacting physiological systems.

METHODS

We develop a conceptual, hypothesis-generating framework grounded in network physiology and systems biology, integrating mitochondrial function, metabolic flexibility, hormetic stress responses, and circadian regulation into a unified architecture of system-level adaptation.

RESULTS

Physiological amplitude is defined as the bounded dynamic range within which coordinated multiscale physiological dynamics are maintained. Aging is conceptualized as a progressive contraction of this accessible range across interconnected biological networks. This framework distinguishes physiological amplitude from variability and resilience by positioning it as a higher-order property emerging from constraint-defined interactions across physiological systems.

CONCLUSION

Physiological amplitude provides an integrative framework for interpreting multiscale physiological dynamics and generates testable hypotheses for quantification using continuous monitoring and network-based analysis. As a candidate systems-level descriptor, it may support the development of integrative biomarkers of aging and metabolic decline, pending empirical validation.

Для цитирования: Sepczynska Grazyna. Physiological amplitude: a systems-level framework for adaptive capacity in aging and metabolism.. Frontiers in aging. 2026. DOI: 10.3389/fragi.2026.1837722.
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