Zhiyue Wang1, Haodong Guo2, Fei Liu2, Xiaoping Wang2, Haige Li2, and Weiyin Vivian Liu3
1Radiology, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, China, 2the Second Affiliated Hospital of Nanjing Medical University, Nanjing, China, 3GE Healthcare, MR Research China, Beijing, China
Synopsis
Keywords: Myocardium, Cardiovascular
Motivation: Explore relationship between cardiac image and duration of dialysis.
Goal(s): To evaluate myocardial damage using CMR in end-stage renal disease (ESRD) patients undergoing hemodialysis and further explore its relationship with duration of dialysis.
Approach: Patients with long- and short-term dialysis were included. CMR parameters (native T1 value and ECV) and two biochemical results (brain pro-natriuretic peptide and troponin T) were compared.
Results: Native T1 value, ECV, brain pro-natriuretic peptide and troponin T were significant different in two groups. Multiple linear regression analysis showed that native T1 value and ECV were independently associated with duration of dialysis and troponin T.
Impact: Quantification
of
myocardial
fibrosis
in ESRD
is challenging. CMR
imaging is useful in the detection of cardiac damage. Longer durations of dialysis may lead to poor
outcomes. Our purpose was to
explore relationship between cardiac image and duration of dialysis.
Introduction
There is an increased risk of
cardiovascular (CV) mortality in populations with end-stage renal disease
(ESRD)[1], and a majority of these patients receive hemodialysis[2]. However,
detecting CV abnormalities early is challenging in some ESRD patients with
preserved left ventricular ejection fraction (LVEF)[3]. Cardiac MR (CMR) native
T1 mapping and extracellular volume (ECV) techniques are sensitive for
evaluating diffuse interstitial myocardial fibrosis[2].
Linear gadolinium-based contrast agents
(GBCAs) have been implicated in the development of nephrogenic systemic
fibrosis (NSF) in patients with ESRD. The European Medicines Agency (EMA) has
determined that macrocyclic formulations (group II GBCAs) are low risk and can
be used in ESRD patients[4]. Findings suggest that the risk of NSF from
low-risk GBCA administration in ESRD is likely less than 0.07%[5]. Therefore,
contrast-enhanced MRI with a low-risk GBCA should not be withheld solely based
on NSF risk[5].
Previous reports have demonstrated
increased T1 times and ECV in ESRD[6] and in patients on hemodialysis[7], yet
the prevalence of myocardial late gadolinium enhancement was found to be
low[8]. These reports also indicated that elevated native T1 in ESRD was
associated with higher levels of serum troponin[6].
Some authors have noted that longer
durations of dialysis sessions may lead to left ventricular hypertrophy[9].
However, few studies have comprehensively evaluated the impact of dialysis
duration on myocardial damage. Therefore, this study aimed to investigate
cardiac involvement by examining CMR native T1 mapping and ECV and to further
explore the relationship between the duration of dialysis and troponin levels.Methods
31 ERSD patients were enrolled[1] in this study and divided in two groups
according to the duration of dialysis, including long-term (≥6 months, 20,
64.5%), and short-term (<6 months, 11, 35.5%).
CMR scans were performed on 3.0-T MR scanner (GE SIGNA™ Premier
3.0T) with a 30-channel body anterior coil. The MR scans included 2-, 3- and 4-chamber views, short-axis
cine images, T1 mapping using the modified look-locker inversion recovery
(MOLLI) sequence (slice thickness 8.0 mm, field of view 300 ×400 mm, flip angle
35°, TE 1.4ms), LGE images acquired at 20 min after a bolus intravenous
injection of 0.15 mmol/kg group II gadolinium-based contrast agent (GBCA)
(gadoteric acid meglumine, Hengrui, Jiangsu, China). Biotech examinations were
measured and dialysis were in all subjects in the same day [4].
The T1 mapping and ECV analyses were
conducted using Segment v4.0 R12067. The mean
T1 in a region of interest in the ventricular cavity was considered the blood
T1. ECV= (1-haematomatic)×(1/post contrast T1 myo-1/native T1 myo)/(1/post
contrast T1 blood-1/native T1 blood)(Figure 1).
Comparisons of parameters between long- and short-term
groups were evaluated by independent sample t test, Chi-square
test or Mann–Whitney U test. A combined parameter model was established through
two-class logistic regression and the predictive effects of native T1
value and ECV on long- or short-term dialysis were calculated. The correlations
between CMR parameters, duration of dialysis and troponin T were evaluated by Pearson
correlation test multiple linear regression. Analysis was calculated using MedCalc 19.1.2 and SPSS 23.0,
figures were made by Graphpad Prism 8.0. P
< 0.05 was considered statistically significant.Results
There were statistical differences in Brain
pro-Natriuretic Peptide (BNP), Troponin T, native T1 value and ECV between
long- and short-time groups (Table 1). Native T1 value and ECV correlated well
with duration of dialysis (r=0.659, 0.721, P<0.05) (Table 2,
Figure 2). The ROC curves showed that the diagnostic efficacy of combined
parameters (AUC = 0.702, P < 0.05) was higher than single parameters
(native T1 value (AUC = 0.613, P < 0.05) and ECV (AUC = 0.651, P
< 0.05)) (Table 3, Figure 3). Multiple linear regression analysis showed
that the native T1 value and ECV were independently associated with duration of
dialysis (beta = 0.891, 0.351, P < 0.05) and troponin T (beta =
0.776, 0.593, P < 0.05) (Table 2, Figure 4).Conclusion
Native T1 value and ECV were found to be
increased in ESRD patients with preserved LVEF under long-term dialysis. The
results of this study suggest that duration of dialysis was associated with and
was an independent risk factor for myocardial damage in ESRD patients
undergoing maintenance hemodialysis.Acknowledgements
No acknowledgement found.References
[1] Graham-Brown
MP, Rutherford E, Levelt E, et al. Native T1 mapping: inter-study,
inter-observer and inter-center reproducibility in hemodialysis patients. J
Cardiovasc Magn Reson. 2017. 19(1): 21.
[2] Qin L,
Gu S, Xiao R, et al. Value of native T1 mapping in the prediction of major
adverse cardiovascular events in hemodialysis patients. Eur Radiol. 2022.
32(10): 6878-6890.
[3] Lin L,
Xie Q, Zheng M, et al. Identification of cardiovascular abnormalities by
multiparametric magnetic resonance imaging in end-stage renal disease patients
with preserved left ventricular ejection fraction. Eur Radiol. 2021. 31(9):
7098-7109.
[4] Edwards
BJ, Laumann AE, Nardone B, et al. Advancing pharmacovigilance through
academic-legal collaboration: the case of gadolinium-based contrast agents and
nephrogenic systemic fibrosis-a Research on Adverse Drug Events and Reports
(RADAR) report. Br J Radiol. 2014. 87(1042): 20140307.
[5] Woolen
SA, Shankar PR, Gagnier JJ, MacEachern MP, Singer L, Davenport MS. Risk of
Nephrogenic Systemic Fibrosis in Patients With Stage 4 or 5 Chronic Kidney
Disease Receiving a Group II Gadolinium-Based Contrast Agent: A Systematic
Review and Meta-analysis. JAMA Intern Med. 2020. 180(2): 223-230.
[6] Rutherford
E, Talle MA, Mangion K, et al. Defining myocardial tissue abnormalities in
end-stage renal failure with cardiac magnetic resonance imaging using native T1
mapping. Kidney Int. 2016. 90(4): 845-52.
[7] Graham-Brown
M, Gulsin GS, Poli F, Parke K, Burton JO, McCann GP. Differences in native T1
and native T2 mapping between patients on hemodialysis and control subjects.
Eur J Radiol. 2021. 140: 109748.
[8] Price
AM, Hayer MK, Vijapurapu R, et al. Myocardial characterization in pre-dialysis
chronic kidney disease: a study of prevalence, patterns and outcomes. BMC
Cardiovasc Disord. 2019. 19(1): 295.
[9] Susantitaphong
P, Koulouridis I, Balk EM, Madias NE, Jaber BL. Effect of frequent or extended
hemodialysis on cardiovascular parameters: a meta-analysis. Am J Kidney Dis.
2012. 59(5): 689-99.