Wilson’s disease is an inherited autosomal recessive multi-systemic disorder characterized by reduced excretion and consequently excessive accumulation of copper in different organs. Cardiac involvement has been considered to be benign in the past. However, cases of cardiac sudden death and an increased incidence of arrhythmias and heart failure have been reported. Just recently, we have demonstrated that even asymptomatic patients exhibit structural disease and autonomic dysfunction of the heart [1, 2].
In a prospective controlled trial, which is the largest to date, we evaluated 61 patients with Wilson’s disease for cardiac manifestation. Wilson’s disease was diagnosed beforehand by hepatic copper content assessment in liver biopsy specimens and laboratory findings (ceruloplasmin level in serum below the limit of normal and 24 h high urinary copper excretion > 100 μg/d). Patients were under stable disease and had no signs of heart failure at the time of examination. All patients underwent cardiac magnetic resonance imaging (cMRI) and were age- and sex-matched to 61 healthy patients.
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Intriguingly, we detected a left ventricular cleft, an invagination penetrating more than 50% wall thickness of the adjoining compact myocardium in diastole, in 20% of the patients (12 out of 61) compared to 5% among control patients (3 out of 61, p = 0.013). Left ventricular clefts became best visible in the late gadolinium enhancement images and cine sequences in cMRI (Fig. 1, Additional file 1: Video S1). They were located in the septal segments (3 out of 12), the inferior (4 out of 12), the lateral (3 out of 12) and the anterior wall (2 out of 12). Additionally, real-time 3D contrast echocardiography was performed, in which an interventricular shunt could be excluded. No correlation between the incidence of cleft and a certain genotype of Wilson’s disease was found (Table 1).
Table 1
Chi-quadrat analysis of Wilson’s disease mutations and left ventricular clefts
Mutation | nm | nc | p-value |
---|---|---|---|
H1069Q | 24 | 6 | 0.39 |
A1135Q | 7 | 2 | 0.53 |
Q1351Stop | 5 | 1 | 0.98 |
M769 V | 1 | 1 | – |
R969Q | 2 | 2 | – |
P1352S | 2 | – | – |
M769H | 5 | – | – |
R1041W | 2 | – | – |
S105Stop | 2 | – | – |
D765N | 2 | – | – |
H643I | 1 | – | – |
Q111Stop | 1 | – | – |
V845S | 1 | – | – |
G1266R | 1 | – | – |
P1273L | 1 | – | – |
G1061E | 1 | – | – |
T1434 M | 1 | – | – |
L1325R | 1 | – | – |
V1282C | 1 | – | – |
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Additional file 1: Video S1. Video showing interventricular cleft.
Myocardial clefts are congenital abnormalities related to myocardial fiber or fascicle disarray. Congenital myocardial clefts or fissures are commonly seen in the basal inferior wall of the left ventricle and the mid to apical segments of the interventricular septum. Petryka et al. studied 686 patients and found these clefts (also called crypts) to be most prevalent in patients with hypertrophic cardiomyopathy (15.6%), myocarditis (15.3%), and arterial hypertension (13.6%). Clefts were also evident, albeit significantly fewer, in 6.7% of the healthy patients [3]. In other studies, the incidence of clefts in hypertrophic cardiomyopathy was even higher with 61 and 81%, respectively [4, 5]. They were proposed to be a prephenotypic marker of hypertrophic cardiomyopathy, that means representing early signs of myocardial alterations in patients that carry a gene defect who have not displayed the phenotype yet. The high variance in prevalence among different studies may be due to the variability of cMRI procedures and the interpretation thereof.
The results of our study suggest that clefts are due to the pathology of Wilson’s disease. All described cases were incidental findings and none of the patients showed other signs of cardiac involvement. The etiology is a matter of speculation. One hypothesis regarding the pathophysiological mechanism of cleft formation was described by Moon and McKenna who speculate that they may represent a sign of abnormal fetal cardiomorphogenesis [5]. However, it remains unknown how pathological accumulations of copper could support this theory and cause them.
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Left ventricular clefts have not been associated to Wilson’s disease before. Previous imaging studies on cardiac manifestation are mainly echocardiography based and have not reported on clefts so far. Likewise, in none of our 12 patients, echocardiography was able to detect any evidence thereof. Echocardiographic visualization can be challenging, particularly if cleft location does not coincide with standard acquisition planes. Therefore, cMRI seems to be more sensitive in detecting structural abnormalities than routine echocardiography.
To conclude, the results of this study suggests the occurrence of left ventricular clefts in cMRI as an early sign of Wilson’s disease in the heart. Large studies with a long observation period are needed for validation. We propose that patients with Wilson’s disease receive cMRI as a standard tool to evaluate cardiac manifestation, specifically with a careful search for left ventricular clefts.
Supplementary information
Supplementary information accompanies this paper at https://doi.org/10.1186/s13023-019-1238-7.
Acknowledgements
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Ethics approval and consent to participate
This study was approved by the local ethics committee. Written informed consent was obtained from all participants. The study protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki.
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Competing interests
The authors declare that they have no competing interests.
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