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A Semi-Automated and Reproducible Biological-Based Method to Quantify Calcium Deposition In Vitro
Published on: June 2, 2022
Classification of chronic kidney disease biomarkers to predict coronary artery calcium
Sterling McPherson1, Celestina Barbosa-Leiker, Robert Short
1Washington State University, College of Nursing, Washington State University, Spokane, WA, USA. smcpherson05@wsu.edu
Insights
Higher serum phosphorus trajectories are linked to increased coronary artery calcification (CAC) even in healthy individuals. Understanding these phosphorus patterns may guide interventions for cardiovascular disease prevention.
Area of Science:
- Nephrology
- Cardiology
- Biostatistics
Background:
- The association between chronic kidney disease (CKD) and coronary artery calcification (CAC) is well-documented, primarily in patients with advanced CKD or ESRD and hyperphosphatemia.
- Previous research often overlooks the role of serum phosphorus in individuals with normal kidney function.
Purpose of the Study:
- To investigate distinct serum phosphorus trajectory classes, adjusted for estimated glomerular filtration rate (eGFR), and their association with CAC in a general community sample.
- To determine if phosphorus levels, even within the typical range, predict CAC development and progression.
Main Methods:
- Utilized growth mixture modeling to classify serum phosphorus and eGFR into four distinct trajectory classes.
- Employed a two-part growth model to predict CAC as both a binary (onset) and continuous (accumulation) outcome based on these phosphorus trajectories.
Main Results:
- Each incremental class increase in phosphorus trajectory was associated with a significant 97.9 Agatston unit increase in CAC.
- This association is comparable in magnitude to established cardiovascular risk factors like age (55.3 AU increase) and inverse to female gender (-75.1 AU decrease).
Conclusions:
- Serum phosphorus trajectories offer refined prediction of CAC, even within conventionally normal ranges.
- Identifying specific phosphorus trajectory classes may establish clinically actionable thresholds for interventions targeting phosphorus reduction to mitigate cardiovascular risk.
Background/Aims:
The link between CKD and CAC has been mostly established by studies of patients who have abnormally high phosphorus levels and advanced CKD or end-stage renal disease. The aim of this study was to examine if there are distinct trajectory classes of serum phosphorus (controlling for eGFR) that are associated CAC in a relatively healthy, community sample.
Methods:
Phosphorus and eGFR were classified as a combined biomarker variable with 4 trajectory classes by growth mixture modeling. This classification variable was subsequently used to predict CAC as both a binary (i.e., onset) and continuous (i.e., accumulation) outcome using a two-part growth model.
Results:
Membership in one class of phosphorus trajectory versus the next lowest level was associated with a 97.9 Agatston unit increase in CAC (p <.001). The magnitude of this finding is similar in size as some primary risk factors for cardiovascular disease, including a 55.3 Agatston unit (p <.001) increase associated with age, and a--75.1 Agatston unit (p <.001) decrease associated with female gender.
Conclusions:
Classification of phosphorus trajectories provides further definition for prediction of CAC within the conventional 'normal' range. Classifying trajectories may help determine clinically-relevant thresholds for interventions aimed at phosphorus reduction.
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