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Common genetic variation is associated with longitudinal decline and network features in behavioral variant frontotemporal degeneration.
Massimo, Lauren; Rennert, Lior; Xie, Sharon X; Olm, Christopher; Bove, Jessica; Van Deerlin, Vivianna; Irwin, David J; Grossman, Murray; McMillan, Corey T.
Afiliación
  • Massimo L; Frontotemporal Degeneration Center, Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA; School of Nursing, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: lmassimo@upenn.edu.
  • Rennert L; Department of Public Health Sciences, Clemson University, Philadelphia, PA, USA. Electronic address: liorr@clemson.edu.
  • Xie SX; Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: sxie@pennmedicine.upenn.edu.
  • Olm C; Frontotemporal Degeneration Center, Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: olm@pennmedicine.upenn.edu.
  • Bove J; Frontotemporal Degeneration Center, Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: Jessica.Bove@pennmedicine.upenn.edu.
  • Van Deerlin V; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Irwin DJ; Frontotemporal Degeneration Center, Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: dirwin@pennmedicine.upenn.edu.
  • Grossman M; Frontotemporal Degeneration Center, Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: mgrossma@pennmedicine.upenn.edu.
  • McMillan CT; Frontotemporal Degeneration Center, Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: mcmillac@pennmedicine.upenn.edu.
Neurobiol Aging ; 108: 16-23, 2021 12.
Article en En | MEDLINE | ID: mdl-34474300
The T allele in rs1768208 located in or near the myelin oligodendrocyte basic protein gene (MOBP) is a risk factor for frontotemporal degeneration pathology. We evaluated the hypothesis that the presence of a T allele in rs1768208 will be associated with rate of cognitive decline in behavioral variant frontotemporal degeneration (bvFTD) related to compromised frontal networks. We studied 81 individuals clinically diagnosed with bvFTD who were genotyped for rs1768208 and coded using a dominant model reflecting the presence (i.e., MOBP +) or absence (MOBP -) of the T risk allele. Linear mixed-effects models assessed the association of genotype on neuropsychological performance over time. Regression analyses examined differences in network structure by MOBP genotype. We found a genotype by time interaction for declining cognitive performance, whereby MOBP + individuals demonstrated faster rates of decline in executive function. The presence of a MOBP risk allele was associated with degradation of white matter network features in the frontal lobe. These findings suggest that individual genetic variation may contribute to heterogeneity in clinical progression.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Demencia Frontotemporal / Estudios de Asociación Genética / Proteínas de la Mielina Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Aging Año: 2021 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Polimorfismo de Nucleótido Simple / Demencia Frontotemporal / Estudios de Asociación Genética / Proteínas de la Mielina Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurobiol Aging Año: 2021 Tipo del documento: Article