Cerebral atrophy in myotonic dystrophy: a voxel based morphometric study

被引:73
作者
Antonini, G
Mainero, C
Romano, A
Giubilei, F
Ceschin, V
Gragnani, F
Morino, S
Fiorelli, M
Soscia, F
Di Pasquale, A
Caramia, F
机构
[1] S Andrea Hosp, Neurol Clin, Neuroradiol Sect, I-00189 Rome, Italy
[2] Univ Roma La Sapienza, Neurol Clin, Fac Med 2, Rome, Italy
[3] Univ Roma La Sapienza, Dept Neurol Sci, Fac Med 1, Neuroradiol Sect, Rome, Italy
[4] Univ Roma La Sapienza, Psychiat Clin, Fac Med 2, Rome, Italy
关键词
D O I
10.1136/jnnp.2003.032417
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Brain involvement in myotonic dystrophy type 1 (DM1) is characterised by cortical atrophy and white matter lesions. We compared the magnetic resonance imaging derived grey matter maps of 22 DM1 patients with those of matched, healthy controls using voxel based morphometry to evaluate the extension of global and regional cortical atrophy in DM1, as well as its relationships with clinical and genetic features. Patients had significantly reduced brain tissue volumes. Grey matter volume was inversely correlated with age; this inverse correlation was significantly stronger in DM1 than in controls. Neither the clinical and genetic characteristics nor white matter lesions were correlated with cortical atrophy. Grey matter atrophy was located mainly in the bilateral frontal and parietal lobes, in the bilateral middle temporal gyrus, and in the left superior temporal and occipital gyrus.
引用
收藏
页码:1611 / 1613
页数:3
相关论文
共 15 条
[1]
INVOLVEMENT OF THE CENTRAL-NERVOUS-SYSTEM IN MYOTONIC-DYSTROPHY [J].
ABE, K ;
FUJIMURA, H ;
TOYOOKA, K ;
YORIFUJI, S ;
NISHIKAWA, Y ;
HAZAMA, T ;
YANAGIHARA, T .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1994, 127 (02) :179-185
[2]
Brain proton magnetic resonance spectroscopy and brain atrophy in myotonic dystrophy [J].
Akiguchi, I ;
Nakano, S ;
Shiino, A ;
Kimura, R ;
Inubushi, T ;
Handa, J ;
Nakamura, M ;
Tanaka, M ;
Oka, T ;
Kimura, J .
ARCHIVES OF NEUROLOGY, 1999, 56 (03) :325-330
[3]
Myotonic dystrophy as a brain disorder [J].
Ashizawa, T .
ARCHIVES OF NEUROLOGY, 1998, 55 (03) :291-293
[4]
COMPUTED TOMOGRAPHIC FINDINGS OF BRAIN AND SKULL IN MYOTONIC-DYSTROPHY [J].
AVRAHAMI, E ;
KATZ, A ;
BORNSTEIN, N ;
KORCZYN, AD .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1987, 50 (04) :435-438
[5]
The clinical and genetic correlates of MRI findings in myotonic dystrophy [J].
Bachmann, G ;
Damian, MS ;
Koch, M ;
Schilling, G ;
Fach, B ;
Stoppler, S .
NEURORADIOLOGY, 1996, 38 (07) :629-635
[6]
CEREBRAL ABNORMALITIES IN MYOTONIC-DYSTROPHY - CEREBRAL BLOOD-FLOW, MAGNETIC-RESONANCE-IMAGING, AND NEUROPSYCHOLOGICAL TESTS [J].
CHANG, L ;
ANDERSON, T ;
MIGNECO, OA ;
BOONE, K ;
MEHRINGER, CM ;
VILLANUEVAMEYER, J ;
BERMAN, N ;
MENA, I .
ARCHIVES OF NEUROLOGY, 1993, 50 (09) :917-923
[7]
T2 relaxometry of brain in myotonic dystrophy [J].
Di Costanzo, A ;
Di Salle, F ;
Santoro, L ;
Bonavita, V ;
Tedeschi, G .
NEURORADIOLOGY, 2001, 43 (03) :198-204
[8]
DECREASED CEREBRAL GLUCOSE-UTILIZATION IN MYOTONIC-DYSTROPHY [J].
FIORELLI, M ;
DUBOC, D ;
MAZOYER, BM ;
BLIN, J ;
EYMARD, B ;
FARDEAU, M ;
SAMSON, Y .
NEUROLOGY, 1992, 42 (01) :91-94
[9]
Friston K.J., 1994, Human Brain Mapping, V2, P189, DOI DOI 10.1002/HBM.460020402
[10]
A voxel-based morphometric study of ageing in 465 normal adult human brains [J].
Good, CD ;
Johnsrude, IS ;
Ashburner, J ;
Henson, RNA ;
Friston, KJ ;
Frackowiak, RSJ .
NEUROIMAGE, 2001, 14 (01) :21-36