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Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
Cardiac valve calcifications and left ventricular hypertrophy in hemodialysis patients
Paweł Strózecki1, Grazyna Odrowaz-Sypniewska, Jacek Manitius
1Department of Nephrology, Hypertension and Internal Diseases, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland. st_pawel@cm.umk.pl
Insights
Cardiac valve calcification is common in hemodialysis patients and linked to left ventricular hypertrophy. This suggests calcification may be an indicator of cardiac changes in patients undergoing dialysis.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Cardiac valve calcification (VC) is prevalent in end-stage renal disease.
- VC is an independent predictor of mortality in peritoneal dialysis patients.
- In hemodialysis (HD) patients, VC's association with mortality diminishes after adjusting for risk factors and left ventricular mass index (LVMI).
Purpose of the Study:
- To investigate the relationship between cardiac valve calcification and left ventricular hypertrophy in hemodialysis patients.
Main Methods:
- Echocardiography was used to assess mitral and aortic valves and calculate LVMI in 65 HD patients.
- Patients were categorized based on the presence and location of valve calcifications.
Main Results:
- 49% of HD patients exhibited valve calcifications (VC(+)).
- Patients with VC were older, had longer HD duration, higher blood pressure, and increased LVMI.
- Patients with calcification in both mitral and aortic valves showed the highest LVMI.
- Higher incidence of Ca x P product > 4.43 mmol²/L² was observed in VC(+) patients.
Conclusions:
- Cardiac valve calcification is associated with left ventricular hypertrophy in hemodialysis patients, especially when both mitral and aortic valves are affected.
- Elevated calcium-x-phosphate product, even transiently, may contribute to cardiac valve calcification in HD patients.
Abstract:
Cardiac valve calcification (VC) is a common finding in end-stage renal disease patients. It was shown recently that VC is an independent predictor for all-cause and cardiovascular mortality in peritoneal dialysis patients. In hemodialysis (HD) patients, VC was associated with all-cause and cardiovascular mortality, but after adjusting for other cardiovascular risk factors and complications, as well as left ventricular mass index (LVMI), it lost significance. The aim of the study was to assess the relationship between VC and left ventricular hypertrophy in hemodialysis patients. Echocardiographic examination with mitral and aortic valves assessment and LVMI calculation was performed in 65 HD patients ages 49+/-12, with duration of HD therapy 38+/-32 months. VC were found in 32 of 65 patients (49%)-Group VC(+), mitral valve calcifications (MVC) in 10, aortic valve calcifications (AVC) in 9, and both valves calcifications (MVC+AVC) in 13 patients. Patients with VC were older, on HD therapy were longer, had higher systolic and pulse pressure, and had higher LVMI. Patients with both VCs had the highest LVMI. No significant differences were found with respect to Ca, P, PTH, and mean Ca x P product, but the incidence of Ca x P product above 4.43 mmol2/L2 was higher in VC(+) compared with those without VCs. VC coexists with left ventricular hypertrophy, particularly when both valves are calcified. Even short-lasting incidents of increased Ca x P product may lead to cardiac VC.
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