Abstract

It is well documented that deteriorating heart function due to deposition of ceroid lipopigment is a significant co-morbidity in Juvenile Neuronal Ceroid Lipofuscinosis (CLN3 disease) although the exact disease mechanisms remain unknown in any NCL form. An increasing frequency of cardiac conduction disorders including severe bradycardia and sinus arrest is seen in the late teens, as is a left ventricular hypertrophy in the early 20s. Only a few case reports of pacemaker implantation have been published, and so far, no long-term follow-up study exists. As new treatment options emerge, more patients will live longer and the need for pacemaker will likely increase, why knowledge of long-term outcome is needed. In the present study, we present the course of six patients from the original Danish CLN3-heart population study (n = 29) published in 2011 in whom pacemaker implantation was indicated from a cardiac point of view. In two cases, the families deselected pacemaker implantation. In four males, aged 19-29 years, all having a good general condition, a dual-chamber pacemaker (St. Jude Medical™ Accent/Assurity MRI™) was implanted in general anesthesia without any complications. At follow-up 9 years later, three were still alive. According to the parents' opinion they still have a good quality of life, now 26, 30, and 36 years old. Pacemaker treatment is safe and may have great impact on quality of life. However, the medical indication for pacemaker treatment is relative and it is important that various aspects, including the patient's general condition and family preferences, are thoroughly discussed before making the final decision.

Highlights

  • The Neuronal Ceroid Lipofuscinoses (NCL) is a group of hereditary diseases characterized by dysfunction of the lysosomes

  • Bradycardia and left ventricular hypertrophy were found in all patients > 20 years old, and in one patient pacemaker treatment was indicated from a cardiologic point of view and in question

  • An increasing frequency of conduction disorders including sinus arrest is seen in these patients in their late teens, along with left ventricular hypertrophy in the early 20 s [7]

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Summary

Introduction

The Neuronal Ceroid Lipofuscinoses (NCL) is a group of hereditary diseases characterized by dysfunction of the lysosomes. The Juvenile Neuronal Ceroid Lipofuscinosis, called CLN3 disease, is a fatal neurodegenerative disease with an estimated incidence range from 0.2 to 7.0 per 100,000 [1]. It is an autosomal recessive disorder caused by a defect in the CLN3 gene, which in the majority of Pacemaker Implantation in CLN3 cases (>85%) is due to a homozygous deletion of exon 7/8 [2]. The disease initially presents with visual impairments and within a few years, decline of cognitive and motor function, behavioral changes and epilepsy follow. Pacemaker implantation in CLN3 disease has only been reported in case studies [4, 5], and no long-term follow-up studies exist. Knowledge of long-term outcome following pacemaker implantation is needed

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