Title:Experience of Miglustat Therapy in Pediatric Patients with Niemann-pick Type C Disease
Volume: 24
Issue: 16
Author(s): Claudia Monteiro*, Anabela Bandeira, Joana Correira, Cristina Garrido, Teresa Temudo and Esmeralda Martins
Affiliation:
- Hospital de Santo António, Pediatric, Portugal
Keywords:
Niemann-pick type C diseasniemann-pick type C disease; miglusta; perinatal; early; infantile (Ei); late-infantile (Li).
Abstract:
Introduction: Niemann-Pick disease type C (NP-C) has an estimated incidence
1/100,000. Is an inherited neurovisceral lysosomal lipid storage disease characterized by progressive
neurological deterioration. Different clinical forms have been defined based on patient
age at onset: perinatal, early infantile (EI), late-infantile (Li), juvenile and adult. Approximately
95% of patients harbour mutations in NPC1, the remainder in NPC2. To date, miglustat is the
only treatment specifically approved in the European Union for the treatment of progressive
neurological manifestations in patients with NP-C.
Methods: We have carried out a retrospective, descriptive study by reviewing the clinical histories,
for all patients diagnosed with NP-C treated with miglustat followed in the Hereditary Metabolism
Diseases Unit of Centro Materno Infantil do Norte – CHPorto.
Results: A total of 6 NP-C patients (4 male and 2 female) were included. Two patients were
sisters. The first patient to start treatment with miglustat was in 2009, the year the drug was approved
in EU. Categorization of patients on clinical grounds according to age at onset of symptoms
identified 1 patient with the EI form of the disease (case 1), 3 patients with the Li form,
(case 3 and 4) and 2 patients with the juvenile form (case 5 and 6). The duration of miglustat
treatment ranged between 4 months to 7 years; therapy was initiated at different ages of patient,
depending on the clinical form. All patients were reported as having neurological manifestations.
Among the neurological symptoms, vertical gaze palsy had been observed in all our cases
except case 4. The gelastic cataplexy crises appeared in all cases except in the juvenile form.
The brain MRI in case 1, 2 and 4 described an increased signal in the white matter and thinning
of the corpus callosum only in case 1, none with alterations in brain spectroscopy. In the cases
1, 2 and 3, non-esterified cholesterol deposits were observed in fibroblasts by histochemical
staining with filipin. The diagnosis was confirmed with the genetic study, finding mutations in
the NPC1 gene in the 6 patients. Cases 1 and 5 died. Case 3 took miglustat for 2 years currently
with a 5-domain NPC with a clinical severity scale of 19, whilecase 4 under therapy with the
drug for 6 years with a clinical severity score of 18, both Li form. While the case 6 had been
taking the medication for 30 months with a clinical severity score of 3.
Conclusion: Sometimes it is difficult to discriminate which are the first neurological symptoms
due to the NP-C disease. The progression of the disease is faster when the symptoms start early.
Data indicating stabilization and a slower rate of progression of the disease; patients with later
onset forms appear as better responders.
