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Published on: August 28, 2018
Primary Hyperparathyroidism Associated With Elevated Coronary Artery Calcium Scores and Increased Cardiovascular Risk
Justin S Bauzon1, Gustavo Romero-Velez2, Jay Ramchand3
1Department of Endocrine Surgery, Cleveland Clinic, Cleveland, Ohio.
Primary hyperparathyroidism (PHPT) is linked to higher coronary artery calcium (CAC) scores, indicating increased cardiovascular risk. Men with PHPT and longer untreated disease duration showed greater calcification, suggesting screening is warranted.
Area of Science:
- Cardiology
- Endocrinology
- Radiology
Background:
- Primary hyperparathyroidism (PHPT) is associated with elevated cardiovascular risk.
- Coronary artery calcium (CAC) scoring quantifies calcific plaque burden for cardiovascular risk assessment.
- The relationship between PHPT and CAC scores remains underexplored.
Purpose of the Study:
- To evaluate the association between PHPT and CAC scores.
- To determine if PHPT independently predicts coronary calcification.
- To explore cardiovascular risk stratification in PHPT patients.
Main Methods:
- Retrospective analysis of 415 patients undergoing CAC scoring (2015-2024).
- Inclusion criteria: concurrent serum calcium and parathyroid hormone levels within one year of CAC testing.
- Comparison of CAC scores (Low-Intermediate: 0-99, High: ≥100) between PHPT and non-PHPT groups; subgroup analyses by risk and PHPT subtype.
Main Results:
- PHPT patients showed a higher prevalence of high CAC scores (≥100) compared to non-PHPT (67% vs 50%, p=.04).
- PHPT independently predicted high CAC scores (OR 1.5, p=.03).
- Male PHPT patients had significantly higher CAC scores than females (median 495 vs 6, p<.01); longer untreated PHPT correlated with severe calcification (OR 1.2, p<.01).
Conclusions:
- PHPT is associated with increased coronary calcific burden and higher cardiovascular event risk.
- Male sex and longer duration of untreated PHPT are linked to greater coronary calcification.
- Routine CAC screening may benefit PHPT populations for cardiovascular risk evaluation.
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