Calcium-Magnesium-Phosphate-Potassium Metabolic Network Dysregulation in Nephrolithiasis: Predictive Model Development and Mechanistic Insights

Read the full article See related articles

Discuss this preprint

Start a discussion What are Sciety discussions?

Listed in

This article is not in any list yet, why not save it to one of your lists.
Log in to save this article

Abstract

Objective To explore the pathophysiological interplay of calcium-magnesium-phosphate-potassium (Ca-Mg-P-K) metabolic networks in nephrolithiasis and establish an integrated risk prediction framework incorporating homeostatic biomarkers. Methods This hospital-based case-control study enrolled 611 nephrolithiasis patients and 624 gender-matched controls. Multivariable logistic regression identified core risk determinants, with model performance rigorously validated through ROC analysis, calibration curves, and decision curve analysis (DCA). A nomogram was constructed to enable dynamic risk visualization. Results The metabolic network-based model demonstrated exceptional discriminative capacity (AUC = 0.812, 95%CI: 0.789–0.836) and calibration accuracy (Brier score = 0.177, Hosmer-Lemeshow p = 0.852). Key predictors included calcium-magnesium ratio (Ca/Mg, aOR = 5.50), calcium-phosphate product (Ca×IP, aOR = 1.82), hypokalemia (aOR = 0.13), BMI ≥ 24, and hemoglobin reduction. The nomogram quantified individualized risk through synergistic scoring, with a score of 240 points identifying high-risk patients (sensitivity = 78.9%, specificity = 73.6%). Subgroup analyses revealed amplified risks in females (Ca/Mg OR = 10.01 vs 6.98) and those in the renal compensatory phase (eGFR > 90 group OR = 10.45). DCA validated the model's clinical utility, revealing net benefit superiority over traditional approaches across 0.3–0.8 risk thresholds. Conclusion This study establishes calcium-magnesium ratio (Ca/Mg) and calcium-phosphate product (Ca×IP) as key indicators of subclinical calcium dysregulation. The nomogram integrates metabolic network interactions to overcome single-marker limitations, with hypokalemia identified as a critical risk amplifier. This model enables early detection of network-level imbalance despite normal individual parameters, offering a clinically actionable tool for personalized nephrolithiasis prevention.

Article activity feed