Key result
Ventricular wall composition explains high patient variability in ECG responses to potassium and calcium changes.
Why the study?
ECG markers correlating with serum potassium and calcium concentrations show high inter-patient variability, which may stem from differences in cell type distribution across the ventricular wall.
Observational (n=29)
No
Inter-patient variability in ECG responses to potassium and calcium variations can be partly explained by differences in ventricular wall cellular composition, which may improve non-invasive electrolyte monitoring in ESRD patients.
Answers are grounded in this paper and cite their sources.
Wall composition may underlie ECG electrolyte variability; animal data leave open translation to clinical monitoring.
Objective: Chronic kidney disease patients have a decreased ability to maintain normal electrolyte concentrations in their blood, which increases the risk for ventricular arrhythmias and sudden cardiac death. Non-invasive monitoring of serum potassium and calcium concentration, [K + ] and [Ca 2+ ], can help to prevent arrhythmias in these patients. Electrocardiogram (ECG) markers that significantly correlate with [K + ] and [Ca 2+ ] have been proposed, but these relations are highly variable between patients. We hypothesized that inter-individual differences in cell type distribution across the ventricular wall can help to explain this variability. Methods: A population of human heart-torso models were built with different proportions of endocardial, midmyocardial and epicardial cells. Propagation of ventricular electrical activity was described by a reaction-diffusion model, with modified Ten Tusscher-Panfilov dynamics. [K + ] and [Ca 2+ ] were varied individually and in combination. Twelve-lead ECGs were simulated and the width, amplitude and morphological variability of T waves and QRS complexes were quantified. Results were compared to measurements from 29 end-stage renal disease (ESRD) patients undergoing hemodialysis (HD). Results: Both simulations and patients data showed that most of the analyzed T wave and QRS complex markers correlated strongly with [K + ] (absolute median Pearson correlation coefficients, r , ranging from 0.68 to 0.98) and [Ca 2+ ] (ranging from 0.70 to 0.98). The same sign and similar magnitude of median r was observed in the simulations and the patients. Different cell type distributions in the ventricular wall led to variability in ECG markers that was accentuated at high [K + ] and low [Ca 2+ ], in agreement with the larger variability between patients measured at the onset of HD. The simulated ECG variability explained part of the measured inter-patient variability. Conclusion: Changes in ECG markers were similarly related to [K + ] and [Ca 2+ ] variations in our models and in the ESRD patients. The high inter-patient ECG variability may be explained by variations in cell type distribution across the ventricular wall, with high sensitivity to variations in the proportion of epicardial cells. Significance: Differences in ventricular wall composition help to explain inter-patient variability in ECG response to [K + ] and [Ca 2+ ]. This finding can be used to improve serum electrolyte monitoring in ESRD patients.
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Bukhari et al. (2023) conducted an observational in End-stage renal disease (n=29). Hemodialysis-induced variations in serum potassium and calcium was evaluated on Correlation of ECG markers with serum potassium and calcium (r 0.68-0.98). Differences in ventricular wall composition, particularly the proportion of epicardial cells, explained the high inter-patient variability in ECG responses to potassium and calcium variations.
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