Structural and functional brain connectivity in presymptomatic familial frontotemporal dementia

被引:67
作者
Dopper, Elise G. P. [1 ,4 ,5 ]
Rombouts, Serge A. R. B. [4 ,7 ,8 ]
Jiskoot, Lize C. [1 ]
den Heijer, Tom [1 ,2 ,9 ]
de Graaf, J. Roos A. [3 ]
de Koning, Inge [3 ]
Hammerschlag, Anke R. [6 ]
Seelaar, Harro [1 ]
Seeley, William W. [10 ,11 ]
Veer, Ilya M. [4 ,7 ,8 ]
van Buchem, Mark A. [4 ,7 ]
Rizzu, Patrizia [6 ]
van Swieten, John C. [1 ,6 ]
机构
[1] Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[2] Erasmus MC, Dept Epidemiol, Rotterdam, Netherlands
[3] Erasmus MC, Dept Neuropsychol, Rotterdam, Netherlands
[4] Leiden Univ, Dept Radiol, Med Ctr, Leiden, Netherlands
[5] Vrije Univ Amsterdam Med Ctr, Dept Neurol, Amsterdam, Netherlands
[6] Vrije Univ Amsterdam Med Ctr, Dept Clin Genet, Amsterdam, Netherlands
[7] Leiden Univ, Leiden Inst Brain & Cognit, Leiden, Netherlands
[8] Leiden Univ, Inst Psychol, Leiden, Netherlands
[9] St Franciscus Gasthuis, Dept Neurol, Rotterdam, Netherlands
[10] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA
[11] Univ Calif San Francisco, Memory & Aging Ctr, San Francisco, CA 94143 USA
关键词
WHITE-MATTER DAMAGE; BEHAVIORAL VARIANT; LOBAR DEGENERATION; HEXANUCLEOTIDE REPEAT; DIAGNOSTIC-CRITERIA; ALZHEIMERS-DISEASE; DIFFUSION; PROGRANULIN; ATROPHY; MRI;
D O I
10.1212/WNL.0b013e31828407bc
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: We aimed to investigate whether cognitive deficits and structural and functional connectivity changes can be detected before symptom onset in a large cohort of carriers of microtubule-associated protein tau and progranulin mutations. Methods: In this case-control study, 75 healthy individuals (aged 20-70 years) with 50% risk for frontotemporal dementia (FTD) underwent DNA screening, neuropsychological assessment, and structural and functional MRI. We used voxel-based morphometry and tract-based spatial statistics for voxelwise analyses of gray matter volume and diffusion tensor imaging measures. Using resting-state fMRI scans, we assessed whole-brain functional connectivity to frontoinsula, anterior midcingulate cortex (aMCC), and posterior cingulate cortex. Results: Although carriers (n = 37) and noncarriers (n = 38) had similar neuropsychological performance, worse performance on Stroop III, Ekman faces, and Happe cartoons correlated with higher age in carriers, but not controls. Reduced fractional anisotropy and increased radial diffusivity throughout frontotemporal white matter tracts were found in carriers and correlated with higher age. Reductions in functional aMCC connectivity were found in carriers compared with controls, and connectivity between frontoinsula and aMCC seeds and several brain regions significantly decreased with higher age in carriers but not controls. We found no significant differences or age correlations in posterior cingulate cortex connectivity. No differences in regional gray matter volume were found. Conclusions: This study convincingly demonstrates that alterations in structural and functional connectivity develop before the first symptoms of FTD arise. These findings suggest that diffusion tensor imaging and resting-state fMRI may have the potential to become sensitive biomarkers for early FTD in future clinical trials. Neurology (R) 2013;80:814-823
引用
收藏
页码:814 / 823
页数:10
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