Slowly progressive behavioral frontotemporal dementia syndrome in a family co-segregating the C9orf72 expansion and a Synaptophysin mutation

Autor(es)

Prota, Joana ^{[1, 2]} ; Rizzi, Liara ^[3] ; Bonadia, Luciana ^{[1, 2]} ; de Souza, Leonardo Cruz ^[4] ; Caramelli, Paulo ^[4] ; Secolin, Rodrigo ^{[1, 2]} ; Lopes-Cendes, Iscia ^{[1, 2]} ; Balthazar, Marcio L. F. ^{[3, 1]}

Afiliação do(s) autor(es)

^[1] Brazilian Inst Neurosci & Neurotechnol BRAINN, Campinas, SP - Brazil

^[2] Univ Campinas UNICAMP, Sch Med Sci, Dept Med Genet & Genom Med, Campinas, SP - Brazil

^[3] Univ Campinas UNICAMP, Dept Neurol, Campinas, SP - Brazil

^[4] Fed Univ Minas Gerais UFMG, Dept Internal Med, Belo Horizonte, MG - Brazil

• Tipo de documento: Artigo Científico
• Fonte: ALZHEIMERS & DEMENTIA; JUL 2021.
• Citações Web of Science: 0

Resumo

Introduction Synaptophysin, already related to X-linked intellectual disability, is expressed mainly in the central nervous system. Studies in humans indicate that the downregulation of synaptophysin could be involved in the development of dementia. Our study presents the first familial case of behavioral variant frontotemporal dementia associated with the co-occurrence of the repeat expansion in C9orf72 and a pathogenic variant in the SYP gene. Methods Exome sequencing and repeat-primed PCR for C9orf72 were performed for two siblings with clinical and imaging findings suggestive of slowly progressive behavioral frontotemporal dementia. Results We found that both siblings have the hexanucleotide expansion in C9orf72 and a null variant in the SYP gene. The most affected sibling presents the putative variant in a hemizygous state. With milder symptoms, his sister has the same pathogenic variant in heterozygosis, compatible with X-linked inheritance. Discussion Our results strengthened previous suggestive evidence that the phenotypes associated with C9orf72 repeat expansion are variable and probably influenced by additional genetic modifiers. We hypothesized that the pathogenic variant in the SYP gene might have modified the typical phenotype associated with the C9orf72 mutation. (AU)

• Processo FAPESP: 18/15571-7 - Mapeando a progressão do declínio cognitivo subjetivo para comprometimento cognitivo leve e demência da Doença de Alzheimer com biomarcadores multimodais
• Beneficiário: Marcio Luiz Figueredo Balthazar
• Modalidade de apoio: Auxílio à Pesquisa - Jovens Pesquisadores - Fase 2
• Processo FAPESP: 13/07559-3 - Instituto Brasileiro de Neurociência e Neurotecnologia - BRAINN
• Beneficiário: Fernando Cendes
• Modalidade de apoio: Auxílio à Pesquisa - Centros de Pesquisa, Inovação e Difusão - CEPIDs