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      Cardiovascular magnetic resonance left ventricular strain in end-stage renal disease patients after kidney transplantation

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          Abstract

          Background

          Cardiovascular disease is a significant cause of morbidity and mortality in patients with end-stage renal disease (ESRD) and kidney transplant (KT) patients. Compared with left ventricular (LV) ejection fraction (LVEF), LV strain has emerged as an important marker of LV function as it is less load dependent. We sought to evaluate changes in LV strain using cardiovascular magnetic resonance imaging (CMR) in ESRD patients who received KT, to determine whether KT may improve LV function.

          Methods

          We conducted a prospective multi-centre longitudinal study of 79 ESRD patients (40 on dialysis, 39 underwent KT). CMR was performed at baseline and at 12 months after KT.

          Results

          Among 79 participants (mean age 55 years; 30% women), KT patients had significant improvement in global circumferential strain (GCS) ( p = 0.007) and global radial strain (GRS) ( p = 0.003), but a decline in global longitudinal strain (GLS) over 12 months ( p = 0.026), while no significant change in any LV strain was observed in the ongoing dialysis group. For KT patients, the improvement in LV strain paralleled improvement in LVEF (57.4 ± 6.4% at baseline, 60.6% ± 6.9% at 12 months; p = 0.001). For entire cohort, over 12 months, change in LVEF was significantly correlated with change in GCS (Spearman’s r = − 0.42, p < 0.001), GRS (Spearman’s r = 0.64, p < 0.001), and GLS (Spearman’s r = − 0.34, p = 0.002). Improvements in GCS and GRS over 12 months were significantly correlated with reductions in LV end-diastolic volume index and LV end-systolic volume index (all p < 0.05), but not with change in blood pressure (all p > 0.10).

          Conclusions

          Compared with continuation of dialysis, KT was associated with significant improvements in LV strain metrics of GCS and GRS after 12 months, which did not correlate with blood pressure change. This supports the notion that KT has favorable effects on LV function beyond volume and blood pessure control. Larger studies with longer follow-up are needed to confirm these findings.

          Electronic supplementary material

          The online version of this article (10.1186/s12968-018-0504-5) contains supplementary material, which is available to authorized users.

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          Most cited references38

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          Clinical epidemiology of cardiovascular disease in chronic renal disease.

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            Hemodialysis-induced cardiac injury: determinants and associated outcomes.

            Hemodialysis (HD)-induced myocardial stunning driven by ischemia is a recognized complication of HD, which can be ameliorated by HD techniques that improve hemodynamics. In nondialysis patients, repeated ischemia leads to chronic reduction in left ventricular (LV) function. HD may initiate and drive the same process. In this study, we examined the prevalence and associations of HD-induced repetitive myocardial injury and long-term effects on LV function and patient outcomes. Seventy prevalent HD patients were assessed for evidence of subclinical myocardial injury at baseline using serial echocardiography and followed up after 12 mo. Intradialytic blood pressure, hematologic and biochemical samples, and patient demographics were also collected at both time points. Sixty-four percent of patients had significant myocardial stunning during HD. Age, ultrafiltration volumes, intradialytic hypotension, and cardiac troponin-T (cTnT) levels were independent determinants associated with its presence. Myocardial stunning was associated with increased relative mortality at 12 mo (P = 0.019). Cox regression analysis showed increased hazard of death in patients with myocardial stunning and elevated cTnT than in patients with elevated cTnT alone (P < 0.02). Patients with myocardial stunning who survived 12 mo had significantly lower LV ejection fractions at rest and on HD (P < 0.001). HD-induced myocardial stunning is common, and may contribute to the development of heart failure and increased mortality in HD patients. Enhanced understanding of dialysis-induced cardiac injury may provide novel therapeutic targets to reduce currently excessive rates of cardiovascular morbidity and mortality.
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              Global Longitudinal Strain Is a Superior Predictor of All-Cause Mortality in Heart Failure With Reduced Ejection Fraction.

              The purpose of this study was to investigate the prognostic value of global longitudinal strain (GLS) in heart failure with reduced ejection fraction (HFrEF) patients in relation to all-cause mortality.
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                Author and article information

                Contributors
                inna.gong@mail.utoronto.ca
                b.alamro@hotmail.com
                prasadr@smh.ca
                connellyp@smh.ca
                Rachel.Wald@uhn.ca
                waldr@smh.ca
                devad@smh.ca
                leong-poih@smh.ca
                nashm@smh.ca
                yuanw@smh.ca
                Lakshman.Gunaratnam@lhsc.on.ca
                Joseph.Kim@uhn.ca
                Charmaine.Lok@uhn.ca
                connellyk@smh.ca
                416-864-5465 , yana@smh.ca
                Journal
                J Cardiovasc Magn Reson
                J Cardiovasc Magn Reson
                Journal of Cardiovascular Magnetic Resonance
                BioMed Central (London )
                1097-6647
                1532-429X
                17 December 2018
                17 December 2018
                2018
                : 20
                : 83
                Affiliations
                [1 ]ISNI 0000 0001 2157 2938, GRID grid.17063.33, University of Toronto, ; Toronto, Canada
                [2 ]GRID grid.415502.7, Department of Medical Imaging, , St Michael’s Hospital, ; Toronto, Canada
                [3 ]GRID grid.415502.7, Keenan Research Centre, , Li Ka Shing Knowledge Institute, St. Michael’s Hospital, ; Toronto, Canada
                [4 ]GRID grid.415502.7, Terrence Donnelly Heart Centre, , St. Michael’s Hospital, ; Toronto, Canada
                [5 ]GRID grid.415502.7, Division of Nephrology, , St Michael’s Hospital, ; Toronto, ON Canada
                [6 ]ISNI 0000 0001 0661 1177, GRID grid.417184.f, Division of Cardiology, , Toronto General Hospital, ; Toronto, Canada
                [7 ]ISNI 0000 0004 1936 8884, GRID grid.39381.30, Division of Nephrology, Department of Medicine, London Health Sciences Centre, Schulich School of Medicine and Dentistry, , Western University, ; London, Canada
                [8 ]ISNI 0000 0001 0661 1177, GRID grid.417184.f, Department of Medicine, Division of Nephrology, , Toronto General Hospital, University Health Network, ; Toronto, Canada
                [9 ]ISNI 0000 0001 0661 1177, GRID grid.417184.f, Department of Medicine, , University Health Network-Toronto General Hospital, ; Toronto, Canada
                [10 ]GRID grid.415502.7, Division of Cardiology, , St. Michael’s Hospital, ; 30 Bond Street, Rm 6-030 Donnelly, Toronto, M5B 1W8 Canada
                Author information
                http://orcid.org/0000-0002-2063-7485
                Article
                504
                10.1186/s12968-018-0504-5
                6296102
                30554567
                4f0c2125-b1f5-409f-afa5-22c9e1379743
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 25 June 2018
                : 9 November 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100004411, Heart and Stroke Foundation of Canada;
                Award ID: HSFNA7077
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Cardiovascular Medicine
                kidney transplant,cardiovascular magnetic resonance,left ventricular peak systolic strain,left ventricular ejection fraction,left ventricular volume

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