• Something wrong with this record ?

Abnormalities in myelination of the superior cerebellar peduncle in patients with schizophrenia and deficits in movement sequencing

J. Hüttlova, Z. Kikinis, M. Kerkovsky, S. Bouix, MA. Vu, N. Makris, M. Shenton, T. Kasparek,

. 2014 ; 13 (4) : 415-424.

Language English Country United States

Document type Journal Article, Research Support, Non-U.S. Gov't

Grant support
NT13437 MZ0 CEP Register

Digital library NLK
Full text - Article
Source

E-resources Online Full text

NLK ProQuest Central from 2002-03-01 to 1 year ago
Medline Complete (EBSCOhost) from 2002-01-01 to 1 year ago
Nursing & Allied Health Database (ProQuest) from 2002-03-01 to 1 year ago
Health & Medicine (ProQuest) from 2002-03-01 to 1 year ago
Psychology Database (ProQuest) from 2002-03-01 to 1 year ago

Deficits in the execution of a sequence of movements are common in schizophrenia. Previous studies reported reduced functional activity in the motor cortex and cerebellum in schizophrenic patients with deficits in movement sequencing. The corticospinal tract (CST) and superior cerebellar peduncle (SCP) are fiber tracts that are involved in movement sequencing. However, the integrity of these tracts has not been evaluated in schizophrenic patients with respect to the performance of movement sequencing yet. Diffusion tensor magnetic resonance images (DT-MRI) were acquired from 24 patients with schizophrenia and 23 matched control subjects. Tractography was applied to reconstruct the CST and SCP and DT-MRI-specific parameters such as fractional anisotropy (FA) and radial diffusivity (RD) were reported. The patient group was further subdivided based on the score of sequencing of complex motor acts subscale of the Neurological Evaluation Scale into those with deficits in sequencing motor acts, the SQ(abn) group (n = 7), and those with normal performance, the SQ(norm) group (n = 17). Schizophrenia patients of the SQ(norm) subgroup had significantly reduced FA and increased RD values in the right CST in comparison to the control group; the SQ(abn) subgroup did not differ from the controls. However, the SQ(abn) subgroup showed impaired integrity of the left SCP, whereas the SQ(norm) subgroup did not. Abnormalities in the right CST in the SQ(norm) and in the left SCP in SQ(abn) groups suggest that the patients with SQ(abn) represent subgroups with distinct deficits. Moreover, these results demonstrate the involvement of the SCP in the pathogenesis of movement sequencing in schizophrenia.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc15014505
003      
CZ-PrNML
005      
20181026105137.0
007      
ta
008      
150420s2014 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s12311-014-0550-y $2 doi
035    __
$a (PubMed)24550129
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Hüttlová, Jitka $u Department of Psychiatry, Masaryk University and University Hospital Brno, Jihlavska 20, 625 00, Brno, Czech Republic. $7 xx0185781
245    10
$a Abnormalities in myelination of the superior cerebellar peduncle in patients with schizophrenia and deficits in movement sequencing / $c J. Hüttlova, Z. Kikinis, M. Kerkovsky, S. Bouix, MA. Vu, N. Makris, M. Shenton, T. Kasparek,
520    9_
$a Deficits in the execution of a sequence of movements are common in schizophrenia. Previous studies reported reduced functional activity in the motor cortex and cerebellum in schizophrenic patients with deficits in movement sequencing. The corticospinal tract (CST) and superior cerebellar peduncle (SCP) are fiber tracts that are involved in movement sequencing. However, the integrity of these tracts has not been evaluated in schizophrenic patients with respect to the performance of movement sequencing yet. Diffusion tensor magnetic resonance images (DT-MRI) were acquired from 24 patients with schizophrenia and 23 matched control subjects. Tractography was applied to reconstruct the CST and SCP and DT-MRI-specific parameters such as fractional anisotropy (FA) and radial diffusivity (RD) were reported. The patient group was further subdivided based on the score of sequencing of complex motor acts subscale of the Neurological Evaluation Scale into those with deficits in sequencing motor acts, the SQ(abn) group (n = 7), and those with normal performance, the SQ(norm) group (n = 17). Schizophrenia patients of the SQ(norm) subgroup had significantly reduced FA and increased RD values in the right CST in comparison to the control group; the SQ(abn) subgroup did not differ from the controls. However, the SQ(abn) subgroup showed impaired integrity of the left SCP, whereas the SQ(norm) subgroup did not. Abnormalities in the right CST in the SQ(norm) and in the left SCP in SQ(abn) groups suggest that the patients with SQ(abn) represent subgroups with distinct deficits. Moreover, these results demonstrate the involvement of the SCP in the pathogenesis of movement sequencing in schizophrenia.
650    _2
$a dospělí $7 D000328
650    _2
$a analýza rozptylu $7 D000704
650    _2
$a anizotropie $7 D016880
650    _2
$a studie případů a kontrol $7 D016022
650    _2
$a mozeček $x patologie $7 D002531
650    _2
$a zobrazování difuzních tenzorů $7 D056324
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé $7 D006801
650    _2
$a počítačové zpracování obrazu $7 D007091
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a pohyb $x fyziologie $7 D009068
650    _2
$a pohybové poruchy $x etiologie $x patologie $7 D009069
650    _2
$a nervové dráhy $x patologie $7 D009434
650    _2
$a neurologické vyšetření $7 D009460
650    _2
$a pons $x patologie $7 D011149
650    _2
$a schizofrenie $x komplikace $x patologie $7 D012559
650    _2
$a bílá hmota $x patologie $7 D066127
650    _2
$a mladý dospělý $7 D055815
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
700    1_
$a Kikinis, Zora
700    1_
$a Kerkovsky, Milos
700    1_
$a Bouix, Sylvain
700    1_
$a Vu, Mai-Anh
700    1_
$a Makris, Nikos
700    1_
$a Shenton, Martha
700    1_
$a Kašpárek, Tomáš, $d 1975- $7 xx0031812
773    0_
$w MED00007845 $t Cerebellum (London, England) $x 1473-4230 $g Roč. 13, č. 4 (2014), s. 415-424
856    41
$u https://pubmed.ncbi.nlm.nih.gov/24550129 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20150420 $b ABA008
991    __
$a 20181026105648 $b ABA008
999    __
$a ok $b bmc $g 1072086 $s 897383
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2014 $b 13 $c 4 $d 415-424 $i 1473-4230 $m Cerebellum $n Cerebellum $x MED00007845
GRA    __
$a NT13437 $p MZ0
LZP    __
$a Pubmed-20150420

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...