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000164026 245__ $$aAnomia is present pre-symptomatically in frontotemporal dementia due to MAPT mutations.
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000164026 520__ $$aA third of frontotemporal dementia (FTD) is caused by an autosomal-dominant genetic mutation in one of three genes: microtubule-associated protein tau (MAPT), chromosome 9 open reading frame 72 (C9orf72) and progranulin (GRN). Prior studies of prodromal FTD have identified impaired executive function and social cognition early in the disease but few have studied naming in detail.We investigated performance on the Boston Naming Test (BNT) in the GENetic Frontotemporal dementia Initiative cohort of 499 mutation carriers and 248 mutation-negative controls divided across three genetic groups: C9orf72, MAPT and GRN. Mutation carriers were further divided into 3 groups according to their global CDR plus NACC FTLD score: 0 (asymptomatic), 0.5 (prodromal) and 1 + (fully symptomatic). Groups were compared using a bootstrapped linear regression model, adjusting for age, sex, language and education. Finally, we identified neural correlates of anomia within carriers of each genetic group using a voxel-based morphometry analysis.All symptomatic groups performed worse on the BNT than controls with the MAPT symptomatic group scoring the worst. Furthermore, MAPT asymptomatic and prodromal groups performed significantly worse than controls. Correlates of anomia in MAPT mutation carriers included bilateral anterior temporal lobe regions and the anterior insula. Similar bilateral anterior temporal lobe involvement was seen in C9orf72 mutation carriers as well as more widespread left frontal atrophy. In GRN mutation carriers, neural correlates were limited to the left hemisphere, and involved frontal, temporal, insula and striatal regions.This study suggests the development of early anomia in MAPT mutation carriers, likely to be associated with impaired semantic knowledge. Clinical trials focused on the prodromal period within individuals with MAPT mutations should use language tasks, such as the BNT for patient stratification and as outcome measures.
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000164026 650_7 $$2Other$$aC9orf72
000164026 650_7 $$2Other$$aCognition
000164026 650_7 $$2Other$$aFrontotemporal dementia
000164026 650_7 $$2Other$$aNaming
000164026 650_7 $$2Other$$aProgranulin
000164026 650_7 $$2Other$$aTau
000164026 650_2 $$2MeSH$$aAnomia: complications
000164026 650_2 $$2MeSH$$aC9orf72 Protein: genetics
000164026 650_2 $$2MeSH$$aFrontotemporal Dementia: complications
000164026 650_2 $$2MeSH$$aFrontotemporal Dementia: diagnostic imaging
000164026 650_2 $$2MeSH$$aFrontotemporal Dementia: genetics
000164026 650_2 $$2MeSH$$aHumans
000164026 650_2 $$2MeSH$$aMutation
000164026 650_2 $$2MeSH$$aProgranulins: genetics
000164026 650_2 $$2MeSH$$atau Proteins: genetics
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000164026 999C5 $$1JS Snowden$$2Crossref$$9-- missing cx lookup --$$a10.1136/jnnp.70.3.323$$p323 -$$tJ Neurol Neurosurg Psychiatry$$uSnowden JS (2001) Distinct behavioural profiles in frontotemporal dementia and semantic dementia. J Neurol Neurosurg Psychiatry 70(3):323–332. https://doi.org/10.1136/jnnp.70.3.323$$v70$$y2001
000164026 999C5 $$1JD Rohrer$$2Crossref$$9-- missing cx lookup --$$a10.1212/WNL.0b013e3181bf997a$$p1451 -$$tNeurology$$uRohrer JD et al (2009) The heritability and genetics of frontotemporal lobar degeneration. Neurology 73(18):1451–1456. https://doi.org/10.1212/WNL.0b013e3181bf997a$$v73$$y2009
000164026 999C5 $$1CJD Hardy$$2Crossref$$9-- missing cx lookup --$$a10.3233/JAD-150806$$p359 -$$tJ Alzheimers Dis$$uHardy CJD et al (2016) The language profile of behavioral variant frontotemporal dementia. J Alzheimers Dis 50(2):359–371. https://doi.org/10.3233/JAD-150806$$v50$$y2016
000164026 999C5 $$1JD Rohrer$$2Crossref$$9-- missing cx lookup --$$a10.1016/S1474-4422(14)70233-9$$p291 -$$tLancet Neurol$$uRohrer JD et al (2015) C9orf72 expansions in frontotemporal dementia and amyotrophic lateral sclerosis. Lancet Neurol 14(3):291–301. https://doi.org/10.1016/S1474-4422(14)70233-9$$v14$$y2015
000164026 999C5 $$1JS Snowden$$2Crossref$$9-- missing cx lookup --$$a10.3109/21678421.2015.1074700$$p497 -$$tAmyotroph Lateral Scler Front Degener$$uSnowden JS et al (2015) Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations. Amyotroph Lateral Scler Front Degener 16(7–8):497–505. https://doi.org/10.3109/21678421.2015.1074700$$v16$$y2015
000164026 999C5 $$1EJ Rogalski$$2Crossref$$9-- missing cx lookup --$$a10.2174/156720509788929264$$p331 -$$tCurr Alzheimer Res$$uRogalski EJ, Mesulam MM (2009) Clinical trajectories and biological features of primary progressive aphasia (PPA). Curr Alzheimer Res 6(4):331–336. https://doi.org/10.2174/156720509788929264$$v6$$y2009
000164026 999C5 $$1KG Ranasinghe$$2Crossref$$9-- missing cx lookup --$$a10.1001/jamaneurol.2016.2016$$p1078 -$$tJAMA Neurol$$uRanasinghe KG et al (2016) Distinct subtypes of behavioral variant frontotemporal dementia based on patterns of network degeneration. JAMA Neurol 73(9):1078–1088. https://doi.org/10.1001/jamaneurol.2016.2016$$v73$$y2016
000164026 999C5 $$1JA Saxon$$2Crossref$$9-- missing cx lookup --$$a10.1136/jnnp-2017-315667$$p675 -$$tJ Neurol Neurosurg Psychiatry$$uSaxon JA et al (2017) Examining the language and behavioural profile in FTD and ALS-FTD. J Neurol Neurosurg Psychiatry 88(8):675–680. https://doi.org/10.1136/jnnp-2017-315667$$v88$$y2017
000164026 999C5 $$1JS Snowden$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.cortex.2019.04.027$$p22 -$$tCortex$$uSnowden JS et al (2019) Naming and conceptual understanding in frontotemporal dementia. Cortex 120:22–35. https://doi.org/10.1016/j.cortex.2019.04.027$$v120$$y2019
000164026 999C5 $$1C McMillan$$2Crossref$$9-- missing cx lookup --$$a10.1159/000077163$$p320 -$$tDement Geriatr Cogn Disord$$uMcMillan C, Gee J, Moore P, Dennis K, DeVita C, Grossman M (2004) Confrontation naming and morphometric analyses of structural mri in frontotemporal dementia. Dement Geriatr Cogn Disord 17(4):320–323. https://doi.org/10.1159/000077163$$v17$$y2004
000164026 999C5 $$1M Grossman$$2Crossref$$9-- missing cx lookup --$$a10.1093/brain/awh075$$p628 -$$tBrain$$uGrossman M et al (2004) What’s in a name: voxel-based morphometric analyses of MRI and naming difficulty in Alzheimer’s disease, frontotemporal dementia and corticobasal degeneration. Brain 127(3):628–649. https://doi.org/10.1093/brain/awh075$$v127$$y2004
000164026 999C5 $$1DM Cash$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neurobiolaging.2017.10.008$$p191 -$$tNeurobiol Aging$$uCash DM et al (2018) Patterns of gray matter atrophy in genetic frontotemporal dementia: results from the GENFI study. Neurobiol Aging 62:191–196. https://doi.org/10.1016/j.neurobiolaging.2017.10.008$$v62$$y2018
000164026 999C5 $$2Crossref$$uKaplan E, Goodglass H, Weintraub S (2001) The Boston Naming Test: Pro- Ed
000164026 999C5 $$1S Weintraub$$2Crossref$$9-- missing cx lookup --$$a10.1097/WAD.0b013e318191c7dd$$p91 -$$tAlzheimer Dis Assoc Disord$$uWeintraub S et al (2009) The Alzheimer’s disease centers’ uniform data set (UDS): the neuropsychological test battery. Alzheimer Dis Assoc Disord 23(2):91–101. https://doi.org/10.1097/WAD.0b013e318191c7dd$$v23$$y2009
000164026 999C5 $$1T Miyagawa$$2Crossref$$9-- missing cx lookup --$$a10.1002/alz.12033$$p106 -$$tAlzheimers Dement J Alzheimers Assoc$$uMiyagawa T et al (2020) Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: data from the ARTFL/LEFFTDS Consortium. Alzheimers Dement J Alzheimers Assoc 16(1):106–117. https://doi.org/10.1002/alz.12033$$v16$$y2020
000164026 999C5 $$1J Ashburner$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neuroimage.2007.07.007$$p95 -$$tNeuroimage$$uAshburner J (2007) A fast diffeomorphic image registration algorithm. Neuroimage 38(1):95–113. https://doi.org/10.1016/j.neuroimage.2007.07.007$$v38$$y2007
000164026 999C5 $$1GR Ridgway$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neuroimage.2008.08.045$$p99 -$$tNeuroimage$$uRidgway GR, Omar R, Ourselin S, Hill DLG, Warren JD, Fox NC (2009) Issues with threshold masking in voxel-based morphometry of atrophied brains. Neuroimage 44(1):99–111. https://doi.org/10.1016/j.neuroimage.2008.08.045$$v44$$y2009
000164026 999C5 $$1IB Malone$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neuroimage.2014.09.034$$p366 -$$tNeuroimage$$uMalone IB et al (2015) Accurate automatic estimation of total intracranial volume: a nuisance variable with less nuisance. Neuroimage 104:366–372. https://doi.org/10.1016/j.neuroimage.2014.09.034$$v104$$y2015
000164026 999C5 $$1LC Jiskoot$$2Crossref$$9-- missing cx lookup --$$a10.1007/s00415-018-8850-7$$p1381 -$$tJ Neurol$$uJiskoot LC et al (2018) Longitudinal cognitive biomarkers predicting symptom onset in presymptomatic frontotemporal dementia. J Neurol 265(6):1381–1392. https://doi.org/10.1007/s00415-018-8850-7$$v265$$y2018
000164026 999C5 $$1G Cheran$$2Crossref$$9-- missing cx lookup --$$a10.1017/S1355617718001005$$p184 -$$tJ Int Neuropsychol Soc$$uCheran G et al (2019) Cognitive indicators of preclinical behavioral variant frontotemporal dementia in MAPT carriers. J Int Neuropsychol Soc 25(2):184–194. https://doi.org/10.1017/S1355617718001005$$v25$$y2019
000164026 999C5 $$1PJ Nestor$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neuroimage.2005.10.008$$p1010 -$$tNeuroimage$$uNestor PJ, Fryer TD, Hodges JR (2006) Declarative memory impairments in Alzheimer’s disease and semantic dementia. Neuroimage 30(3):1010–1020. https://doi.org/10.1016/j.neuroimage.2005.10.008$$v30$$y2006
000164026 999C5 $$1K Moore$$2Crossref$$9-- missing cx lookup --$$a10.1080/23279095.2020.1716357$$tAppl Neuropsychol Adult$$uMoore K et al (2020) A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort. Appl Neuropsychol Adult. https://doi.org/10.1080/23279095.2020.1716357$$y2020
000164026 999C5 $$1M Mion$$2Crossref$$9-- missing cx lookup --$$a10.1093/brain/awq272$$p3256 -$$tBrain$$uMion M et al (2010) What the left and right anterior fusiform gyri tell us about semantic memory. Brain 133(11):3256–3268. https://doi.org/10.1093/brain/awq272$$v133$$y2010
000164026 999C5 $$1ML Gorno-Tempini$$2Crossref$$9-- missing cx lookup --$$a10.1002/ana.10825$$p335 -$$tAnn Neurol$$uGorno-Tempini ML et al (2004) Cognition and anatomy in three variants of primary progressive aphasia. Ann Neurol 55(3):335–346. https://doi.org/10.1002/ana.10825$$v55$$y2004
000164026 999C5 $$1JD Rohrer$$2Crossref$$9-- missing cx lookup --$$a10.1212/WNL.0b013e3181a4124e$$p1562 -$$tNeurology$$uRohrer JD et al (2009) Patterns of cortical thinning in the language variants of frontotemporal lobar degeneration. Neurology 72(18):1562–1569. https://doi.org/10.1212/WNL.0b013e3181a4124e$$v72$$y2009
000164026 999C5 $$1E Rogalski$$2Crossref$$9-- missing cx lookup --$$a10.1523/JNEUROSCI.5544-10.2011$$p3344 -$$tJ Neurosci$$uRogalski E et al (2011) Anatomy of language impairments in primary progressive aphasia. J Neurosci 31(9):3344–3350. https://doi.org/10.1523/JNEUROSCI.5544-10.2011$$v31$$y2011
000164026 999C5 $$1SM Wilson$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.neuroimage.2017.12.068$$p62 -$$tNeuroimage$$uWilson SM, Bautista A, McCarron A (2018) Convergence of spoken and written language processing in the superior temporal sulcus. Neuroimage 171:62–74. https://doi.org/10.1016/j.neuroimage.2017.12.068$$v171$$y2018
000164026 999C5 $$1ML Seghier$$2Crossref$$9-- missing cx lookup --$$a10.1177/1073858412440596$$p43 -$$tNeuroscientist$$uSeghier ML (2013) The angular gyrus: multiple functions and multiple subdivisions. Neuroscientist 19(1):43–61. https://doi.org/10.1177/1073858412440596$$v19$$y2013
000164026 999C5 $$1JR Hodges$$2Crossref$$9-- missing cx lookup --$$a10.1016/S1474-4422(07)70266-1$$p1004 -$$tLancet Neurol$$uHodges JR, Patterson K (2007) Semantic dementia: a unique clinicopathological syndrome. Lancet Neurol 6(11):1004–1014. https://doi.org/10.1016/S1474-4422(07)70266-1$$v6$$y2007
000164026 999C5 $$1SA Savage$$2Crossref$$9-- missing cx lookup --$$a10.1016/j.cortex.2012.09.014$$p1823 -$$tCortex$$uSavage SA, Ballard KJ, Piguet O, Hodges JR (2013) Bringing words back to mind—improving word production in semantic dementia. Cortex 49(7):1823–1832. https://doi.org/10.1016/j.cortex.2012.09.014$$v49$$y2013