Quantifying change in individual subjects affected by frontotemporal lobar degeneration using automated longitudinal MRI volumetry

被引:30
作者
Frings, Lars [1 ]
Mader, Irina [2 ]
Landwehrmeyer, Bernhard G. [3 ]
Weiller, Cornelius [4 ]
Huell, Michael [1 ]
Huppertz, Hans-Juergen [5 ]
机构
[1] Univ Freiburg, Dept Psychiat & Psychotherapy, Ctr Geriatr & Gerontol Freiburg, Freiburg Brain Imaging, D-79106 Freiburg, Germany
[2] Univ Freiburg, Univ Med Ctr, Neuroradiol Sect, D-79106 Freiburg, Germany
[3] Univ Ulm, Dept Neurol, D-7900 Ulm, Germany
[4] Univ Freiburg, Univ Med Ctr, Dept Neurol, D-79106 Freiburg, Germany
[5] Swiss Epilepsy Ctr, Zurich, Switzerland
关键词
dementia; frontotemporal lobar degeneration; MRI; postprocessing; volumetry; PRIMARY-PROGRESSIVE-APHASIA; ALZHEIMERS-DISEASE; SEMANTIC DEMENTIA; CEREBRAL ATROPHY; BRAIN ATROPHY; PATTERNS; RATES; MORPHOMETRY; VARIANTS; AD;
D O I
10.1002/hbm.21304
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
A novel method of automated MRI volumetry was used to study regional atrophy and disease progression in repeated MRI measurements of patients with frontotemporal lobar degeneration (FTLD). Fifty-nine structural MRI data sets of 17 clinically diagnosed FTLD patients were acquired over up to 30 months in intervals of 6 months and compared with data of 30 age-matched healthy controls. Patients were further subgrouped into behavioral variant FTLD (bvFTLD), progressive nonfluent aphasia (PNFA), and semantic dementia (SemD). Gray matter (GM) volumes of frontal lobes (FL) and temporal lobes (TL) were determined by voxel-based volumetry based on SPM5 algorithms and a probabilistic brain atlas. MRI volumetry revealed frontal and temporal GM atrophy across FTLD patients, with further progression over time. Significant side asymmetry of TL volumes was found in SemD. The ratio of TL to FL volumes was significantly reduced in SemD and increased in bvFTLD. Using this ratio, 6/7 SemD patients and 5/6 bvFTLD patients could be correctly differentiated. TL/FL ratios in bvFTLD and SemD further diverged significantly over a time span of only 6 months. Rates of temporal GM loss per 6 months were 34% in SemD, and 2.5% for frontal GM loss in bvFTLD, and thereby clearly exceeded published cerebral volume loss in healthy elderly subjects. The study presents a fully automated, observer-independent volumetric assessment of regional atrophy which allows differentiation of FTLD subgroups. Its sensitivity for atrophy progressioneven in such short intervals like 6 monthsmight benefit future clinical trials as treatment outcome measure. Hum Brain Mapp, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:1526 / 1535
页数:10
相关论文
共 33 条
[1]
Voxel-based morphometry - The methods [J].
Ashburner, J ;
Friston, KJ .
NEUROIMAGE, 2000, 11 (06) :805-821
[2]
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17 [J].
Baker, Matt ;
Mackenzie, Ian R. ;
Pickering-Brown, Stuart M. ;
Gass, Jennifer ;
Rademakers, Rosa ;
Lindholm, Caroline ;
Snowden, Julie ;
Adamson, Jennifer ;
Sadovnick, A. Dessa ;
Rollinson, Sara ;
Cannon, Ashley ;
Dwosh, Emily ;
Neary, David ;
Melquist, Stacey ;
Richardson, Anna ;
Dickson, Dennis ;
Berger, Zdenek ;
Eriksen, Jason ;
Robinson, Todd ;
Zehr, Cynthia ;
Dickey, Chad A. ;
Crook, Richard ;
McGowan, Eileen ;
Mann, David ;
Boeve, Bradley ;
Feldman, Howard ;
Hutton, Mike .
NATURE, 2006, 442 (7105) :916-919
[3]
Atrophy progression in semantic dementia with asymmetric temporal involvement: A tensor-based morphometry study [J].
Brambati, S. M. ;
Rankin, K. P. ;
Narvid, J. ;
Seeley, W. W. ;
Dean, D. ;
Rosen, H. J. ;
Miller, B. L. ;
Ashburner, J. ;
Gorno-Tempini, M. L. .
NEUROBIOLOGY OF AGING, 2009, 30 (01) :103-111
[4]
A tensor based morphometry study of longitudinal gray matter contraction in FTD [J].
Brambati, Simona M. ;
Renda, Natasha C. ;
Rankin, Katherine P. ;
Rosen, Howard J. ;
Seeley, William W. ;
Ashburner, John ;
Weiner, Michael W. ;
Miller, Bruce L. ;
Gomo-Tempini, Maria Luisa .
NEUROIMAGE, 2007, 35 (03) :998-1003
[5]
Rates of global and regional cerebral atrophy in AD and frontotemporal dementia [J].
Chan, D ;
Fox, NC ;
Jenkins, R ;
Scahill, RI ;
Crum, WR ;
Rossor, MN .
NEUROLOGY, 2001, 57 (10) :1756-1763
[6]
Development of an MRI rating scale for multiple brain regions: comparison with volumetrics and with voxel-based morphometry [J].
Davies, R. Rhys ;
Scahill, Victoria L. ;
Graham, Andrew ;
Williams, Guy B. ;
Graham, Kim S. ;
Hodges, John R. .
NEURORADIOLOGY, 2009, 51 (08) :491-503
[7]
Automated MRI measures identify individuals with mild cognitive impairment and Alzheimers disease [J].
Desikan, Rahul S. ;
Cabral, Howard J. ;
Hess, Christopher P. ;
Dillon, William P. ;
Glastonbury, Christine M. ;
Weiner, Michael W. ;
Schmansky, Nicholas J. ;
Greve, Douglas N. ;
Salat, David H. ;
Buckner, Randy L. ;
Fischl, Bruce .
BRAIN, 2009, 132 :2048-2057
[8]
Different regional patterns of cortical thinning in Alzheimer's disease and frontotemporal dementia [J].
Du, An-Tao ;
Schuff, Norbert ;
Kramer, Joel H. ;
Rosen, Howard J. ;
Gorno-Tempini, Maria Luisa ;
Rankin, Katherine ;
Miller, Bruce L. ;
Weiner, Michael W. .
BRAIN, 2007, 130 :1159-1166
[9]
One-Year Brain Atrophy Evident in Healthy Aging [J].
Fjell, Anders M. ;
Walhovd, Kristine B. ;
Fennema-Notestine, Christine ;
McEvoy, Linda K. ;
Hagler, Donald J. ;
Holland, Dominic ;
Brewer, James B. ;
Dale, Anders M. .
JOURNAL OF NEUROSCIENCE, 2009, 29 (48) :15223-15231
[10]
Normative estimates of cross-sectional and longitudinal brain volume decline in aging and AD [J].
Fotenos, AF ;
Snyder, AZ ;
Girton, LE ;
Morris, JC ;
Buckner, RL .
NEUROLOGY, 2005, 64 (06) :1032-1039