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Pérez‐Oliveira, Sergio; Álvarez, Ignacio; Rosas, Irene; Menendez‐González, Manuel; Blázquez‐Estrada, Marta; Aguilar, Miquel; Corte, Daniela; Buongiorno, Mariateresa; Molina‐Porcel, Laura; Aldecoa, Iban; Martí, María J.; Sánchez‐Juan, Pascual; Infante, Jon; González‐Aramburu, Isabel; García‐González, Pablo; Rosende‐Roca, Maitée; Boada, Mercè; Ruiz, Agustín; Periñán, María Teresa; Macías‐García, Daniel; Muñoz‐Delgado, Laura; Gómez‐Garre, Pilar; Mir, Pablo; Clarimón, Jordi; Lleo, Alberto; Alcolea, Daniel; De la Casa‐Fages, Beatriz; Duarte, Israel; Álvarez, Victoria; Pastor, Pau
Movement disorders, September 2022, Letnik: 37, Številka: 9Journal Article
Background Previous studies suggest a link between CAG repeat number in the HTT gene and non‐Huntington neurodegenerative diseases. Objective The aim is to analyze whether expanded HTT CAG alleles and/or their size are associated with the risk for developing α‐synucleinopathies or their behavior as modulators of the phenotype. Methods We genotyped the HTT gene CAG repeat number and APOE‐Ɛ isoforms in a case‐control series including patients with either clinical or neuropathological diagnosis of α‐synucleinopathy. Results We identified three Parkinson's disease (PD) patients (0.30%) and two healthy controls (0.19%) carrying low‐penetrance HTT repeat expansions whereas none of the dementia with Lewy bodies (DLB) or multisystem atrophy (MSA) patients carried pathogenic HTT expansions. In addition, a clear increase in the number of HTT CAG repeats was found among DLB and PD groups influenced by the male gender and also by the APOE4 allele among DLB patients. HTT intermediate alleles' (IAs) distribution frequency increased in the MSA group compared with controls (8.8% vs. 3.9%, respectively). These differences were indeed statistically significant in the MSA group with neuropathological confirmation. Two MSA HTT CAG IAs carriers with 32 HTT CAG repeats showed isolated polyQ inclusions in pons and basal nuclei, which are two critical structures in the neurodegeneration of MSA. Conclusions Our results point to a link between HTT CAG number, HTT IAs, and expanded HTT CAG repeats with other non‐HD brain pathology and support the hypothesis that they can share common neurodegenerative pathways. © 2022 International Parkinson and Movement Disorder Society. HTT intermediate alleles' (IAs) frequency is increased in multisystem atrophy. Two MSA IAs carriers showed isolated polyQ inclusions in pons and basal nuclei, which are two critical structures in the neurodegeneration of MSA. Our results point to a link between HTT CAG repeats with other non‐HD brain pathology.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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in: SICRIS
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