Gene specific effects on brain volume and cognition of TMEM106B in frontotemporal lobar degeneration.
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Vandebergh Marijne, Ramos Eliana Marisa, Corriveau-Lecavalier Nick, Ramanan Vijay K, Kornak John, Mester Carly, Kolander Tyler, Brushaber Danielle, Staffaroni Adam M, Geschwind Daniel, Wolf Amy, Kantarci Kejal, Gendron Tania F, Petrucelli Leonard, Van den Broeck Marleen, Wynants Sarah, Baker Matthew C, Borrego-Écija Sergi, Appleby Brian, Barmada Sami, Bozoki Andrea, Clark David, Darby R Ryan, Dickerson Bradford C, Domoto-Reilly Kimiko, Fields Julie A, Galasko Douglas R, Ghoshal Nupur, Graff-Radford Neill, Grant Ian M, Honig Lawrence S, Hsiung Ging-Yuek Robin, Huey Edward D, Irwin David, Knopman David S, Kwan Justin Y, Léger Gabriel C, Litvan Irene, Masdeu Joseph C, Mendez Mario F, Onyike Chiadi, Pascual Belen, Pressman Peter, Ritter Aaron, Roberson Erik D, Snyder Allison, Sullivan Anna Campbell, Tartaglia M Carmela, Wint Dylan, Heuer Hilary W, Forsberg Leah K, Boxer Adam L, Rosen Howard J, Boeve Bradley F, Rademakers Rosa
Аннотация
METHODS: Participants were enrolled through the ARTFL/LEFFTDS Longitudinal Frontotemporal Lobar Degeneration (ALLFTD) study, which includes symptomatic and presymptomatic individuals with a pathogenic mutation in C9orf72, GRN, MAPT, VCP, TBK1, TARDBP, symptomatic non-mutation carriers, and non-carrier family controls. All participants were genotyped for the TMEM106B rs1990622 SNP. Cross-sectionally, linear mixed-effects models were fitted to assess an association between TMEM106B and genetic group interaction with each outcome measure (gray matter volume and UDS3-EF for cognition), adjusting for education, age, sex and CDR®+NACC-FTLD sum of boxes. Subsequently, associations between TMEM106B and each outcome measure were investigated within the genetic group. For longitudinal modeling, linear mixed-effects models with time by TMEM106B predictor interactions were fitted.
RESULTS: The minor allele of TMEM106B rs1990622, linked to a decreased risk of FTD, associated with greater gray matter volume in GRN mutation carriers under the recessive dosage model. This was most pronounced in the thalamus in the left hemisphere, with a retained association when considering presymptomatic GRN mutation carriers only. The minor allele of TMEM106B rs1990622 also associated with greater cognitive scores among all C9orf72 mutation carriers and in presymptomatic C9orf72 mutation carriers, under the recessive dosage model.
DISCUSSION: We identified associations of TMEM106B with gray matter volume and cognition in the presence of GRN and C9orf72 mutations. This further supports TMEM106B as modifier of TDP-43 pathology. The association of TMEM106B with outcomes of interest in presymptomatic GRN and C9orf72 mutation carriers could additionally reflect TMEM106B's impact on divergent pathophysiological changes before the appearance of clinical symptoms.