scholarly journals Corrigendum to ‘Single-subject classification of presymptomatic frontotemporal dementia mutation carriers user multimodal MRI’ NeuroImage: Clinical 20 (2018) 188–196

2019 ◽  
Vol 22 ◽  
pp. 101717
Author(s):  
Rogier A. Feis ◽  
Mark J.R.J. Bouts ◽  
Jessica L. Panman ◽  
Lize C. Jiskoot ◽  
Elise G.P. Dopper ◽  
...  
2018 ◽  
Vol 20 ◽  
pp. 188-196 ◽  
Author(s):  
Rogier A. Feis ◽  
Mark J.R.J. Bouts ◽  
Jessica L. Panman ◽  
Lize C. Jiskoot ◽  
Elise G.P. Dopper ◽  
...  

2019 ◽  
Vol 22 ◽  
pp. 101718 ◽  
Author(s):  
Rogier A. Feis ◽  
Mark J.R.J. Bouts ◽  
Jessica L. Panman ◽  
Lize C. Jiskoot ◽  
Elise G.P. Dopper ◽  
...  

NeuroImage ◽  
2011 ◽  
Vol 55 (2) ◽  
pp. 514-521 ◽  
Author(s):  
Andres H. Neuhaus ◽  
Florin C. Popescu ◽  
Cristian Grozea ◽  
Eric Hahn ◽  
Constanze Hahn ◽  
...  

Author(s):  
Xueling Suo ◽  
Du Lei ◽  
Nannan Li ◽  
Wenbin Li ◽  
Graham J. Kemp ◽  
...  

AbstractWhile previous structural-covariance studies have an advanced understanding of brain alterations in Parkinson's disease (PD), brain–behavior relationships have not been examined at the individual level. This study investigated the topological organization of grey matter (GM) networks, their relation to disease severity, and their potential imaging diagnostic value in PD. Fifty-four early-stage PD patients and 54 healthy controls (HC) underwent structural T1-weighted magnetic resonance imaging. GM networks were constructed by estimating interregional similarity in the distributions of regional GM volume using the Kullback–Leibler divergence measure. Results were analyzed using graph theory and network-based statistics (NBS), and the relationship to disease severity was assessed. Exploratory support vector machine analyses were conducted to discriminate PD patients from HC and different motor subtypes. Compared with HC, GM networks in PD showed a higher clustering coefficient (P = 0.014) and local efficiency (P = 0.014). Locally, nodal centralities in PD were lower in postcentral gyrus and temporal-occipital regions, and higher in right superior frontal gyrus and left putamen. NBS analysis revealed decreased morphological connections in the sensorimotor and default mode networks and increased connections in the salience and frontoparietal networks in PD. Connection matrices and graph-based metrics allowed single-subject classification of PD and HC with significant accuracy of 73.1 and 72.7%, respectively, while graph-based metrics allowed single-subject classification of tremor-dominant and akinetic–rigid motor subtypes with significant accuracy of 67.0%. The topological organization of GM networks was disrupted in early-stage PD in a way that suggests greater segregation of information processing. There is potential for application to early imaging diagnosis.


2019 ◽  
Vol 90 (11) ◽  
pp. 1207-1214 ◽  
Author(s):  
Rogier A Feis ◽  
Mark J R J Bouts ◽  
Frank de Vos ◽  
Tijn M Schouten ◽  
Jessica L Panman ◽  
...  

BackgroundMultimodal MRI-based classification may aid early frontotemporal dementia (FTD) diagnosis. Recently, presymptomatic FTD mutation carriers, who have a high risk of developing FTD, were separated beyond chance level from controls using MRI-based classification. However, it is currently unknown how these scores from classification models progress as mutation carriers approach symptom onset. In this longitudinal study, we investigated multimodal MRI-based classification scores between presymptomatic FTD mutation carriers and controls. Furthermore, we contrasted carriers that converted during follow-up (‘converters’) and non-converting carriers (‘non-converters’).MethodsWe acquired anatomical MRI, diffusion tensor imaging and resting-state functional MRI in 55 presymptomatic FTD mutation carriers and 48 healthy controls at baseline, and at 2, 4, and 6 years of follow-up as available. At each time point, FTD classification scores were calculated using a behavioural variant FTD classification model. Classification scores were tested in a mixed-effects model for mean differences and differences over time.ResultsPresymptomatic mutation carriers did not have higher classification score increase over time than controls (p=0.15), although carriers had higher FTD classification scores than controls on average (p=0.032). However, converters (n=6) showed a stronger classification score increase over time than non-converters (p<0.001).ConclusionsOur findings imply that presymptomatic FTD mutation carriers may remain similar to controls in terms of MRI-based classification scores until they are close to symptom onset. This proof-of-concept study shows the promise of longitudinal MRI data acquisition in combination with machine learning to contribute to early FTD diagnosis.


2014 ◽  
Vol 347 (1-2) ◽  
pp. 262-267 ◽  
Author(s):  
Jorne Laton ◽  
Jeroen Van Schependom ◽  
Jeroen Gielen ◽  
Jeroen Decoster ◽  
Tim Moons ◽  
...  

2021 ◽  
pp. jnnp-2020-323541
Author(s):  
Jessica L Panman ◽  
Vikram Venkatraghavan ◽  
Emma L van der Ende ◽  
Rebecca M E Steketee ◽  
Lize C Jiskoot ◽  
...  

ObjectiveProgranulin-related frontotemporal dementia (FTD-GRN) is a fast progressive disease. Modelling the cascade of multimodal biomarker changes aids in understanding the aetiology of this disease and enables monitoring of individual mutation carriers. In this cross-sectional study, we estimated the temporal cascade of biomarker changes for FTD-GRN, in a data-driven way.MethodsWe included 56 presymptomatic and 35 symptomatic GRN mutation carriers, and 35 healthy non-carriers. Selected biomarkers were neurofilament light chain (NfL), grey matter volume, white matter microstructure and cognitive domains. We used discriminative event-based modelling to infer the cascade of biomarker changes in FTD-GRN and estimated individual disease severity through cross-validation. We derived the biomarker cascades in non-fluent variant primary progressive aphasia (nfvPPA) and behavioural variant FTD (bvFTD) to understand the differences between these phenotypes.ResultsLanguage functioning and NfL were the earliest abnormal biomarkers in FTD-GRN. White matter tracts were affected before grey matter volume, and the left hemisphere degenerated before the right. Based on individual disease severities, presymptomatic carriers could be delineated from symptomatic carriers with a sensitivity of 100% and specificity of 96.1%. The estimated disease severity strongly correlated with functional severity in nfvPPA, but not in bvFTD. In addition, the biomarker cascade in bvFTD showed more uncertainty than nfvPPA.ConclusionDegeneration of axons and language deficits are indicated to be the earliest biomarkers in FTD-GRN, with bvFTD being more heterogeneous in disease progression than nfvPPA. Our data-driven model could help identify presymptomatic GRN mutation carriers at risk of conversion to the clinical stage.


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