ArticleAging cell2026
Acid-Base Dysregulation Links Aging Metabolism to Frailty.
Article in Aging cell, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Authors and funding
3 authors.
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Abstract
Frailty denotes a state of high vulnerability and, as proposed by Fried and colleagues, arises from "energetic collapse" across multiple physiological systems, in which altered energy metabolism undermines resilience. We suggest that dysregulation of acid-base balance represents a critical yet underappreciated mechanism driving this collapse. With aging, cumulative stress burden diminishes the capacity for intracellular and extracellular acid buffering, renal acid excretion and ventilatory reserve, leading to impaired pH homeostasis, reduced mitochondrial ATP production, and declining cellular and organismal efficiency. Skeletal muscle, bone, liver, and kidney cooperate to mobilize the base reserves and redirect amino acid metabolism to enhance renal acid elimination. But this adaptation occurs at the expense of musculoskeletal integrity-a hallmark of aging. The shrinking iceberg metaphor illustrates frailty progression. Repeated stressors erode the acid buffer and energy reserve. Incorporating acid-base dysregulation into frailty models highlights new therapeutic targets-including diet, exercise and buffering strategies to preserve reserve and delay frailty progression.
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