Myocardial fibrosis and diastolic dysfunction in patients on chronic haemodialysis

Nephrol Dial Transplant. 2010 Jun;25(6):1950-4. doi: 10.1093/ndt/gfp747. Epub 2010 Jan 14.

Abstract

Background: Left ventricular (LV) diastolic dysfunction is linked to myocardial collagen content in many cardiac diseases. There are no data regarding such relationship in patients with end-stage renal disease (ESRD) undergoing haemodialysis.

Methods: Twenty-five patients with ESRD undergoing haemodialysis were studied by echocardiography. LV diastolic function was investigated by Doppler echocardiography, by analysing LV filling velocities at rest and during loading manoeuvres, which represent an estimate of LV filling pressure. According to the Doppler pattern, LV filling pressure in a given patient was judged to be normal or slightly increased or to be moderately or severely increased. The presence of myocardial fibrosis was estimated by ultrasound tissue characterization with integrated backscatter, which in diastole correlates with the collagen content of the myocardium.

Results: Integrated backscatter was higher in patients with moderate or severely increased than in patients with normal or slightly increased LV filling pressure (integrated backscatter: 51.0 +/- 9.8 vs 41.6 +/- 5.6%; P = 0.008). Integrated backscatter was a strong and independent determinant of diastolic dysfunction (odds ratio = 1.212; P = 0.040).

Conclusion: Our data support the hypothesis that, in a selected population of patients with ESRD undergoing haemodialysis, myocardial fibrosis is associated with LV diastolic myocardial properties.

MeSH terms

  • Adult
  • Aged
  • Diastole
  • Echocardiography, Doppler
  • Female
  • Fibrosis
  • Humans
  • Kidney Failure, Chronic / complications*
  • Kidney Failure, Chronic / diagnostic imaging
  • Kidney Failure, Chronic / therapy*
  • Male
  • Middle Aged
  • Myocardium / pathology*
  • Renal Dialysis*
  • Ventricular Dysfunction, Left / complications*
  • Ventricular Dysfunction, Left / diagnostic imaging
  • Ventricular Dysfunction, Left / physiopathology
  • Young Adult