End-stage Renal Disease Clinical Trial
Official title:
Impact Of In-Centre Nocturnal Hemodialysis On Cardiac Remodeling In End-Stage Renal Disease: A Long-Term Follow-Up Study
Background: In 2010, approximately 39000 Canadians had end-stage renal disease (ESRD), and
the prevalence rate of dialysis has increased by 189% over the past 2 decades. The annual
mortality rate remains high at ~15%, and cardiovascular events are the leading cause of
death. Intensification of conventional dialysis schedules has been the major focus in recent
years. Currently, most Canadian dialysis patients receive conventional in-center
hemodialysis (CHD), which is administered as a 3-4 hour session 3/week. Recent research has
focused on home nocturnal hemodialysis (8 hours of hemodialysis at home for 5-6
nights/week), which may have substantial cardiovascular benefits, including regression of
left ventricular (LV) hypertrophy, improved LV ejection fraction and enhanced blood pressure
control. Nevertheless, this dialysis modality is only feasible in a highly selected minority
of ESRD patients who can self-manage their dialysis treatment at home. In-center nocturnal
hemodialysis (INHD), administered as 7-8 hours of hemodialysis in hospital for 3nights/week,
represents a promising and practical alternative for many dialysis patients. In a Canadian
Institutes for Health Research (CIHR) supported cohort study, the investigators have
recruited 67 patients and have completed 1-year follow-up. There is a compelling need for
longer-term follow-up, since all the published randomized controlled trials are of short
duration (6-12 months), while renal replacement therapy is a life-long treatment.
Furthermore, the observed large variability of cardiac remodeling in individual ESRD
patients remains poorly understood. Therefore, the current study is an extended follow-up
phase (5 years from enrollment) on the completed 1-year follow-up period and the purpose of
this study is to objectively evaluate the long-term effects of more intensified hemodialysis
treatment which the INHD modality offers.
Need for Long-term and Generalizable Data: In contrast to the seminal Alberta trial which
showed a significant LV mass reduction with home nocturnal hemodialysis, the recently
reported Frequent Hemodialysis Network Nocturnal Trial demonstrated only a trend toward
reduction in LV mass. It is likely that the highly selected participants, inadequate trial
power and duration (12 months) account for the observed results. Currently, it is unknown
whether INHD, which is less intensive but more feasible for most ESRD patients, is
associated with similar cardiovascular benefits in the long term.
Objective:
1. To determine the long-term effects of INHD on (i) LV mass; (ii) global and regional LV
systolic and diastolic function; (iii) myocardial tissue characteristics; (iv) left
atrial structure and function; (v) selected cardiovascular biomarkers in ESRD patients.
2. To examine the determinants and mechanisms of cardiac remodeling in ESRD
Hypothesis: Conversion to INHD is associated with sustained improvements in cardiovascular
structure and function, as compared to conventional hemodialysis (CHD) in patients with
end-stage renal disease (ESRD).
Study Design and Population: This will be a 2-centre, prospective, longitudinal cohort study
of 67 adult ESRD patients (INHD subjects and CHD controls) enrolled in the original study.
All eligible participants who provide consent will undergo cardiac Magnetic Resonance
Imaging (MRI) examination and bloodwork at 5 years since enrollment in the study. Other
follow-up procedures include the following -electrocardiogram, transthoracic echocardiogram,
ambulatory blood pressure monitoring, lateral x-ray of the aorta, and completion of
questionnaires.
Outcome: The primary endpoint is the change in LV mass over 5 years, as measured by cardiac
MRI. Secondary endpoints include LV size, global and regional diastolic and systolic
function, left atrial size and function, changes in myocardial tissue characteristics, blood
pressure, serum troponin, norepinephrine, Brain Natriuretic Peptide (BNP), high sensitivity
C-Reactive Protein (hsCRP), interleukin-6, matrix metalloproteinases, fibroblast growth
factor-23, fetuin-A, transforming growth factor-beta, connective tissue growth factor,
clinical events, and quality of life.
Significance: The provision of an enhanced dialysis regimen has emerged as the most
promising avenue through which to modify the dismal cardiovascular outcomes in patients
receiving chronic hemodialysis. INHD represents a means of administering such therapy to a
broad spectrum of dialysis patients for whom home therapies would not be feasible. This
study will be the first to precisely define the long-term cardiac effects of intensified
dialysis and to elucidate the mechanisms of cardiac remodeling in ESRD, using cardiac MRI
and other novel biomarkers. These important observational findings may have a major impact
on the optimal management and outcome of ESRD patients in the real world.
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