Semi-automatic brain region extraction (SABRE) reveals superior cortical and deep gray matter atrophy in MS

NeuroImage ◽  
2006 ◽  
Vol 29 (2) ◽  
pp. 505-514 ◽  
Author(s):  
D.A. Carone ◽  
R.H.B. Benedict ◽  
M.G. Dwyer ◽  
D.L. Cookfair ◽  
B. Srinivasaraghavan ◽  
...  
PLoS ONE ◽  
2018 ◽  
Vol 13 (11) ◽  
pp. e0206939 ◽  
Author(s):  
Renxin Chu ◽  
Gloria Kim ◽  
Shahamat Tauhid ◽  
Fariha Khalid ◽  
Brian C. Healy ◽  
...  

2018 ◽  
Vol 40 (1) ◽  
pp. 99-106 ◽  
Author(s):  
G. Pontillo ◽  
S. Cocozza ◽  
R. Lanzillo ◽  
C. Russo ◽  
M.D. Stasi ◽  
...  

Author(s):  
G. Pontillo ◽  
M. Petracca ◽  
S. Monti ◽  
M. Quarantelli ◽  
C. Criscuolo ◽  
...  

2018 ◽  
Vol 40 (1) ◽  
pp. 107-108 ◽  
Author(s):  
M.M. Schoonheim ◽  
J.J.G. Geurts

2021 ◽  
Vol 11 (10) ◽  
pp. 1296
Author(s):  
Simonas Jesmanas ◽  
Rymantė Gleiznienė ◽  
Mindaugas Baranauskas ◽  
Vaidas Matijošaitis ◽  
Daiva Rastenytė

Multiple associations between impaired olfactory performance and regional cortical and deep gray matter atrophy have been reported in separate studies of patients with Alzheimer’s disease (AD), Parkinson’s disease (PD), and of the healthy elderly. We aimed to evaluate such possible associations among these populations in a unified manner. Twenty AD, twenty PD patients’ and twenty healthy age- and sex-matched controls’ odor identification performance was assessed with the Lithuanian adaptation of the Sniffin’ Sticks 12 odor identification test, followed by morphometric gray matter analysis by MRI using FreeSurfer. AD patients had significantly lower cognitive performance than both PD patients and the healthy elderly, as evaluated with the Mini-Mental State Examination (MMSE). Odor identification performance was significantly worse in AD and PD patients compared with the healthy elderly; AD patients performed slightly worse than PD patients, but the difference was not statistically significant. Among patients with AD, worse odor identification performance was initially correlated with atrophy of multiple cortical and deep gray matter regions known to be involved in olfactory processing, however, only two measures—decreased thicknesses of the right medial and left lateral orbitofrontal cortices—remained significant after adjustment for possible confounders (age, MMSE score, and global cortical thickness). Among patients with PD and the healthy elderly we found no similar statistically significant correlations. Our findings support the key role of the orbitofrontal cortex in odor identification among patients with AD, and suggest that correlations between impaired odor identification performance and regional gray matter atrophy may be relatively more pronounced in AD rather than in PD.


2017 ◽  
Vol 39 (1) ◽  
pp. 46-53 ◽  
Author(s):  
A. Meijerman ◽  
H. Amiri ◽  
M.D. Steenwijk ◽  
M.A. Jonker ◽  
R.A. van Schijndel ◽  
...  

Neurology ◽  
2019 ◽  
Vol 93 (14) ◽  
pp. e1348-e1359 ◽  
Author(s):  
Anand J.C. Eijlers ◽  
Iris Dekker ◽  
Martijn D. Steenwijk ◽  
Kim A. Meijer ◽  
Hanneke E. Hulst ◽  
...  

ObjectiveTo determine which pathologic process could be responsible for the acceleration of cognitive decline during the course of multiple sclerosis (MS), using longitudinal structural MRI, which was related to cognitive decline in relapsing-remitting MS (RRMS) and progressive MS (PMS).MethodsA prospective cohort of 230 patients with MS (179 RRMS and 51 PMS) and 59 healthy controls was evaluated twice with 5-year (mean 4.9, SD 0.94) interval during which 22 patients with RRMS converted to PMS. Annual rates of cortical and deep gray matter atrophy as well as lesion volume increase were computed on longitudinal (3T) MRI data and correlated to the annual rate of cognitive decline as measured using an extensive cognitive evaluation at both time points.ResultsThe deep gray matter atrophy rate did not differ between PMS and RRMS (−0.82%/year vs −0.71%/year, p = 0.11), while faster cortical atrophy was observed in PMS (−0.87%/year vs −0.48%/year, p < 0.01). Similarly, faster cognitive decline was observed in PMS compared to RRMS (p < 0.01). Annual cognitive decline was related to the rate of annual lesion volume increase in stable RRMS (r = −0.17, p = 0.03) to the rate of annual deep gray matter atrophy in converting RRMS (r = 0.50, p = 0.02) and annual cortical atrophy in PMS (r = 0.35, p = 0.01).ConclusionsThese results indicate that cortical atrophy and cognitive decline accelerate together during the course of MS. Substrates of cognitive decline shifted from worsening lesional pathology in stable RRMS to deep gray matter atrophy in converting RRMS and to accelerated cortical atrophy in PMS only.


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