Skip Navigation



NDT Advance Access published online on October 12, 2005

Nephrology Dialysis Transplantation, doi:10.1093/ndt/gfi075
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
21/1/125    most recent
gfi075v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Yumi Hayashi, S.
Right arrow Articles by Seeberger, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Yumi Hayashi, S.
Right arrow Articles by Seeberger, A.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© The Author [2005]. Published by Oxford University Press on behalf of ERA-EDTA. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org
Received March 27, 2005
Accepted July 22, 2005


Original Articles

Left ventricular function in patients with chronic kidney disease evaluated by colour tissue Doppler velocity imaging

Shirley Yumi Hayashi 1, Morteza Rohani 2, Bengt Lindholm 3, Lars-Åke Brodin 4, Britta Lind 2, Peter Barany 5, Anders Alvestrand 5, and Astrid Seeberger 5*

1 Department of Medical Engineering, Royal Institute of Technology, Stockholm, Sweden; Division of Renal Medicine, Stockholm, Sweden
2 Department of Clinical Physiology, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden
3 Division of Baxter Novum, Department of Clinical Science, Stockholm, Sweden
4 Department of Medical Engineering, Royal Institute of Technology, , Stockholm, Sweden; Department of Clinical Physiology, Karolinska Institutet, Karolinska University Hospital Huddinge, Stockholm, Sweden
5 Division of Renal Medicine, Stockholm, Sweden

* To whom correspondence should be addressed.
Astrid Seeberger, E-mail: astrid.seeberger{at}klinvet.ki.se



  Abstract

Background. Cardiovascular disease is the leading cause of death in chronic kidney disease (CKD) patients. Tissue Doppler velocity imaging (TVI) is a new objective method that accurately quantifies myocardial tissue velocities, deformation, time intervals and left ventricular (LV) filling pressure. In this study, TVI was compared with conventional echocardiography for the assessment of left ventricular (LV) function in pre-dialysis patients with different stages of CKD. The results obtained by TVI were used to analyse possible relationships between LV function and clinical factors such as hyperparathyroidism and hypertension that could influence LV function.

Methods. Conventional echocardiography and TVI images were recorded in 40 patients (36 men and 4 women, mean age 60±14 years, range 28-80 years) and in 27 healthy controls (21 men and 6 women, mean age 58±17 years, range 28-82 years). Twenty-two patients had mild/moderate CKD (CCr >29 ml/min; Group 1) and 18 patients had severe CKD (CCr ≤29 ml/min; Group 2). Using TVI, the myocardial tissue velocities (v; cm/s) for isovolumetric contraction (IVCv), peak systole (PSv), early (E') and late (A') diastolic filling velocities as well as strain rate (SR), mitral annulus displacement, isovolumetric relaxation time (IVRT) and LV filling pressure were estimated using TVI. The average of six LV wall measurements was used to evaluate LV global function.

Results. Using TVI, we were able to identify significantly more patients with diastolic dysfunction than using conventional echocardiography (33 vs 26, P<0.05). There was no difference in the prevalence of diastolic dysfunction between Group 1 and 2. However, using TVI, Group 2 CKD patients had lower E' velocities (6.2±1.9 vs 8.0±2.9 cm/s, P<0.05) and higher IVRT (137.4±13 vs 88.2±26 ms, P<0.001) in comparison with controls, indicating more accentuated diastolic dysfunction. Systolic blood pressure (SBP) was associated with E' velocities ( {rho} = -0.68, P<0.005) and E'/A' was strongly associated with SBP ( {rho} = -0.60; P<0.01) and PTH ( {rho} = -0.64, P<0.005) in Group 2. Using conventional echocardiography, there was no difference in the prevalence of systolic and diastolic dysfunction between patients with and without LVH. However, using TVI, patients with LVH had significantly lower IVCv (2.8±1.3 vs 3.8±1.5 and 3.8±1.5 cm/s, P<0.05) and PSv (5.5±1.0 vs 6.3±1.2 and 6.4±1.3 cm/s, P<0.05) compared with patients without LVH and controls, and they also had lower E' velocities (7.1±2.7 vs 8.0±2.9 cm/s, P<0.05) compared with controls, indicating disturbances in systolic and diastolic left ventricular function.

Conclusions. TVI provided additional information on left ventricular function in CKD patients. In patients with advanced renal failure, TVI revealed more accentuated diastolic dysfunction associated with increased systolic blood pressure (SBP) and increased levels of PTH. TVI also demonstrated disturbances in contractility and contraction in patients with LVH, which could not be detected by conventional echocardiography.

Keywords: chronic kidney disease; parathyroid hormone; predialysis; tissue Doppler echocardiography.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nephrol Dial TransplantHome page
M. Essig, B. Escoubet, D. de Zuttere, F. Blanchet, F. Arnoult, E. Dupuis, C. Michel, F. Mignon, F. Mentre, C. Clerici, et al.
Cardiovascular remodelling and extracellular fluid excess in early stages of chronic kidney disease
Nephrol. Dial. Transplant., January 1, 2008; 23(1): 239 - 248.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.