Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases
Eliana Marisa Ramos, Deepika Reddy Dokuru, Victoria Van Berlo, Kevin Wojta, Qing Wang, Alden Y Huang, Sandeep Deverasetty, Yue Qin, Marka van Blitterswijk, Jazmyne Jackson, Brian Appleby, Yvette Bordelon, Patrick Brannelly, Danielle E Brushaber, Bradford Dickerson, Susan Dickinson, Kimiko Domoto-Reilly, Kelley Faber, Julie Fields, Jamie Fong, Tatiana Foroud, Leah K Forsberg, Ralitza Gavrilova, Nupur Ghoshal, Jill Goldman, Jonathan Graff-Radford, Neill Graff-Radford, Ian Grant, Murray Grossman, Hilary W Heuer, Ging-Yuek R Hsiung, Edward Huey, David Irwin, Kejal Kantarci, Anna Karydas, Daniel Kaufer, Diana Kerwin, David Knopman, John Kornak, Joel H Kramer, Walter Kremers, Walter Kukull, Irene Litvan, Peter Ljubenkov, Codrin Lungu, Ian Mackenzie, Mario F Mendez, Bruce L Miller, Chiadi Onyike, Alexander Pantelyat, Rodney Pearlman, Len Petrucelli, Madeline Potter, Katherine P Rankin, Katya Rascovsky, Erik D Roberson, Emily Rogalski, Leslie Shaw, Jeremy Syrjanen, Maria Carmela Tartaglia, Nadine Tatton, Joanne Taylor, Arthur Toga, John Q Trojanowski, Sandra Weintraub, Bonnie Wong, Zbigniew Wszolek, Rosa Rademakers, Brad F Boeve, Howard J Rosen, Adam L Boxer, ARTFL/LEFFTDS consortium, Giovanni Coppola, Eliana Marisa Ramos, Deepika Reddy Dokuru, Victoria Van Berlo, Kevin Wojta, Qing Wang, Alden Y Huang, Sandeep Deverasetty, Yue Qin, Marka van Blitterswijk, Jazmyne Jackson, Brian Appleby, Yvette Bordelon, Patrick Brannelly, Danielle E Brushaber, Bradford Dickerson, Susan Dickinson, Kimiko Domoto-Reilly, Kelley Faber, Julie Fields, Jamie Fong, Tatiana Foroud, Leah K Forsberg, Ralitza Gavrilova, Nupur Ghoshal, Jill Goldman, Jonathan Graff-Radford, Neill Graff-Radford, Ian Grant, Murray Grossman, Hilary W Heuer, Ging-Yuek R Hsiung, Edward Huey, David Irwin, Kejal Kantarci, Anna Karydas, Daniel Kaufer, Diana Kerwin, David Knopman, John Kornak, Joel H Kramer, Walter Kremers, Walter Kukull, Irene Litvan, Peter Ljubenkov, Codrin Lungu, Ian Mackenzie, Mario F Mendez, Bruce L Miller, Chiadi Onyike, Alexander Pantelyat, Rodney Pearlman, Len Petrucelli, Madeline Potter, Katherine P Rankin, Katya Rascovsky, Erik D Roberson, Emily Rogalski, Leslie Shaw, Jeremy Syrjanen, Maria Carmela Tartaglia, Nadine Tatton, Joanne Taylor, Arthur Toga, John Q Trojanowski, Sandra Weintraub, Bonnie Wong, Zbigniew Wszolek, Rosa Rademakers, Brad F Boeve, Howard J Rosen, Adam L Boxer, ARTFL/LEFFTDS consortium, Giovanni Coppola
Abstract
Introduction: The Advancing Research and Treatment for Frontotemporal Lobar Degeneration (ARTFL) and Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects (LEFFTDS) consortia are two closely connected studies, involving multiple North American centers that evaluate both sporadic and familial frontotemporal dementia (FTD) participants and study longitudinal changes.
Methods: We screened the major dementia-associated genes in 302 sporadic and 390 familial (symptomatic or at-risk) participants enrolled in these studies.
Results: Among the sporadic patients, 16 (5.3%) carried chromosome 9 open reading frame 72 (C9orf72), microtubule-associated protein tau (MAPT), and progranulin (GRN) pathogenic variants, whereas in the familial series we identified 207 carriers from 146 families. Of interest, one patient was found to carry a homozygous C9orf72 expansion, while another carried both a C9orf72 expansion and a GRN pathogenic variant. We also identified likely pathogenic variants in the TAR DNA binding protein (TARDBP), presenilin 1 (PSEN1), and valosin containing protein (VCP) genes, and a subset of variants of unknown significance in other rare FTD genes.
Discussion: Our study reports the genetic characterization of a large FTD series and supports an unbiased sequencing screen, irrespective of clinical presentation or family history.
Keywords: C9orf72; GRN; MAPT; familial; frontotemporal dementia; sporadic.
© 2020 the Alzheimer's Association.
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Source: PubMed