[Heart valve calcification in patients with chronic kidney disease]

Klinicheskaia Meditsina
|August 13, 2009
PubMed

Insights

Heart valve calcification (HVC) in chronic kidney disease (CKD) patients is linked to atherosclerosis and diabetes, particularly in those not on hemodialysis. For hemodialysis patients, HVC correlates with mineral imbalances and longer treatment duration, negatively impacting heart function.

Area of Science:

  • Nephrology
  • Cardiology
  • Biochemistry

Background:

  • Heart valve calcification (HVC) is a growing concern in chronic kidney disease (CKD) patients.
  • Understanding factors contributing to HVC and its hemodynamic impact is crucial for managing CKD complications.

Purpose of the Study:

  • To identify factors associated with HVC in CKD patients.
  • To investigate the effect of HVC on intracardiac hemodynamics in CKD patients.

Main Methods:

  • Echocardiography, cardiomonitoring, carotid intima-media thickness, mineral bone density, and abdominal aorta calcification imaging were used.
  • 377 CKD patients (control) and 132 on hemodialysis (HD) were analyzed.

Main Results:

  • HVC prevalence was 38.9% in HD patients and 27.3% in non-HD CKD patients.
  • HVC was associated with older age, coronary heart disease, cardiac insufficiency, aortic calcinosis, and inflammation in both groups.
  • In non-HD patients, HVC linked to thicker intima-media, lower GFR, higher blood pressure, and diabetes. In HD patients, HVC linked to longer HD duration, higher PTH/calcium, and lower forearm MOC.
  • HVC correlated with valve stenosis/regurgitation, atrial enlargement, and ventricular wall thickening.
  • Multifactor analysis identified age, phosphorus/sodium imbalance, and HD duration for HD patients; intima-media thickness and diabetes for non-HD patients.

Conclusions:

  • In non-HD CKD patients, HVC is primarily associated with atherosclerosis exacerbated by reduced GFR and diabetes.
  • In HD patients, HVC is linked to phosphorus/sodium imbalance and atherosclerosis.
  • HVC negatively affects intracardiac hemodynamics, with decreased MOC observed in HVC patients.

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