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Allostatic Load is a construct used To quantify the cumulative burden of exposure to stress that, over the course of an individual�s
life, exert a toll on the body�s physiological functions, predisposing to the development of various chronic ailments and conditions.
The systemic physiological dysregulation resulting from increasing allostatic load can be quantified through chemical imbalances in
various organ systems. Many studies have attempted to do this by combining multiple clinical parameters (e.g. albumin, C-reactive
protein, cholesterol, etc.) to produce univariate indices that serve as measures of allostatic load. The general validity of these indices
has been confirmed through studies showing they are good predictors of adverse health outcomes, mortality, hospital utilization and
age-related pathologies. They have also used to demonstrate the existence of socioeconomic and demographic health disparities.
In this study, we show the value of including red blood cell distribution width (RDW) among the panel of clinical parameters used
to calculate allostatic load. RDW quantifies the degree of heterogeneity in erythrocyte volume and has shown strong correlations
with mortality and a broad spectrum of diseases. A review of the existing literature on allostatic load reveals its underutilization
in this area, despite being a standard component of blood count panels. Using Cox Proportional Hazards regression and Adaptive
Index models, we show that calculating allostatic load using RDW (in addition to the common set of clinical parameters typically
used in most studies) yields a significantly improved index. It demonstrates a superior ability to predict mortality, health status and
comorbidities than the standard version currently in use.
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