Structural Brain Changes in Pre-Clinical FTD MAPT Mutation Carriers

被引:10
|
作者
Dominguez-Vivero, Clara [1 ]
Wu, Liwen [2 ]
Lee, Seonjoo [2 ]
Manoochehri, Masood [1 ]
Cines, Sarah [1 ,7 ]
Brickman, Adam M. [1 ]
Rizvi, Batool [1 ]
Chesebro, Anthony [1 ]
Gazes, Yunglin [1 ]
Fallon, Emer [5 ]
Lynch, Timothy [5 ]
Heidebrink, Judith L. [6 ]
Paulson, Henry [6 ]
Goldman, Jill S. [1 ]
Huey, Edward [1 ,3 ,4 ]
Cosentino, Stephanie [1 ]
机构
[1] Columbia Univ, Dept Neurol, Cognit Neurosci Div, Taub Inst,GH Sergievsky Ctr, New York, NY USA
[2] Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, New York, NY USA
[3] Columbia Univ, Dept Psychiat, New York, NY USA
[4] Columbia Univ, New York State Psychiat Inst, New York, NY USA
[5] Dublin Neurol Inst, Dublin, Ireland
[6] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[7] Fairleigh Dickinson Univ, Teaneck, NJ USA
关键词
Atrophy; brain atrophy; early detection; frontotemporal lobar degeneration; MAPT mutation; FRONTOTEMPORAL LOBAR DEGENERATION; WHITE-MATTER HYPERINTENSITIES; PRESYMPTOMATIC MAPT; DEMENTIA; ATROPHY; TAU; PROGRANULIN; PATTERNS; C9ORF72; GENFI;
D O I
10.3233/JAD-190820
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Frontotemporal dementia (FTD) is the second most common cause of early-onset neurodegenerative dementia. Several studies have focused on early imaging changes in FTD patients, but once subjects meet full criteria for FTD diagnosis, structural changes are generally widespread. Objective: This study aims to determine the earliest structural brain changes in asymptomatic MAPT MUTATION carriers. Methods: This is a cross-sectional multicenter study comparing global and regional brain volume and white matter integrity in a group of MAPT mutation preclinical carriers and controls. Participants belong to multiple generations of six families with five MAPT mutations. All participants underwent a medical examination, neuropsychological tests, genetic analysis, and a magnetic resonance scan (3T, scout, T1-weighted image followed by EPI (BOLD), MPRAGE, DTI, FLAIR, and ASL sequences). Results: Volumes of five cortical and subcortical areas were strongly correlated with mutation status: temporal lobe (left amygdala, left temporal pole), cingulate cortex (left rostral anterior cingulate gyrus, right posterior cingulate), and the lingual gyrus in the occipital lobe. We did not find significant differences in whole brain volume, white matter hyperintensities volume, and white matter integrity using DTI analysis. Conclusion: Temporal lobe, cingulate cortex and the lingual gyrus seem to be early targets of the disease and may serve as biomarkers for FTD prior to overt symptom onset.
引用
收藏
页码:595 / 606
页数:12
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