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Familial Alzheimer’s disease associated with heterozygous <i>NPC1</i> mutation

Diego LopergoloDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, ItalySilvia BianchiDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, ItalyGian Nicola GallusDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, ItalySara LocciUniversity of SienaBarbara PucciDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, ItalyValerio LeoniLaboratory of Clinical Chemistry, Hospital of Desio, ASST Brianza, School of Medicine and Surgery, University of Milano Bicocca, Milan, ItalyDaniele GaspariniDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, ItalyElisa TardelliUnit of Nuclear Medicine, Department of Diagnostic Imaging, PO - S. Stefano, Azienda U.S.L. Toscana Centro, Prato, italyA. ChincariniNational Institute of Nuclear Physics ((INFN), Genoa, ItalyStelvio SestiniUnit of Nuclear Medicine, Department of Diagnostic Imaging, PO - S. Stefano, Azienda U.S.L. Toscana Centro, Prato, italyFilippo M. SantorelliMolecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Stella Maris Foundation, Calambrone, ItalyHenrik ZetterbergClinical Neurochemistry Laboratory, Sahlgrenska University Hospital, Mölndal, SwedenNicola De StefanoDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, ItalyAndrea MignarriDepartment of Medicine, Surgery and Neurosciences, University of Siena, Siena, Italy
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Introduction NPC1 mutations are responsible for Niemann-Pick disease type C (NPC), a rare autosomal recessive neurodegenerative disease. Patients harbouring heterozygous NPC1 mutations may rarely show parkinsonism or dementia. Here, we describe for the first time a large family with an apparently autosomal dominant late-onset Alzheimer’s disease (AD) harbouring a novel heterozygous NPC1 mutation. Methods All the five living siblings belonging to the family were evaluated. We performed clinical evaluation, neuropsychological tests, assessment of cerebrospinal fluid markers of amyloid deposition, tau pathology and neurodegeneration (ATN), structural neuroimaging and brain amyloid-positron emission tomography. Oxysterol serum levels were also tested. A wide next-generation sequencing panel of genes associated with neurodegenerative diseases and a whole exome sequencing analysis were performed. Results We detected the novel heterozygous c.3034G&gt;T (p.Gly1012Cys) mutation in NPC1 , shared by all the siblings. No other point mutations or deletions in NPC1 or NPC2 were found. In four siblings, a diagnosis of late-onset AD was defined according to clinical characterisation and ATN biomarkers (A+, T+, N+) and serum oxysterol analysis showed increased 7-ketocholesterol and cholestane-3β,5α,6β-triol. Discussion We describe a novel NPC1 heterozygous mutation harboured by different members of a family with autosomal dominant late-onset amnesic AD without NPC-associated features. A missense mutation in homozygous state in the same aminoacidic position has been previously reported in a patient with NPC with severe phenotype. The alteration of serum oxysterols in our family corroborates the pathogenic role of our NPC1 mutation. Our work, illustrating clinical and biochemical disease hallmarks associated with NPC1 heterozygosity in patients affected by AD, provides relevant insights into the pathogenetic mechanisms underlying this possible novel association.

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