Structural Brain Correlations of Visuospatial and Visuoperceptual Tests in Parkinson’s Disease
Open accessAbstract
Background: Diagnosis of mild cognitive impairment in Parkinson’s disease (PD) is relevant because it is a marker for evolution to dementia. However, the selection of suitable tests to evaluate separate cognitive domains in mild cognitive impairment related to PD remains an open question. The current work aims to investigate the neuroanatomical correlates of several visuospatial/visuoperceptual tests using the same sample and a multimodal MRI approach. Methods: The study included 36 PD patients and 20 healthy subjects matched for age, sex, and education. The visuospatial/visuoperceptual tests selected were: Pentagon Copying Test (PCT), Judgment of Line Orientation Test (JLOT), Visual Form Discrimination Test (VFDT), Facial Recognition Test (FRT), Symbol Digit Modalities Test (SMDT), and clock copying task (CLOX2). FreeSurfer was used to assess cortical thickness, and tract-based spatial statistics was used for fractional anisotropy analysis. Results: Lower performance in the PCT, JLOT, and SDMT was associated with extensive cortical thickness reductions in lateral parietal and temporal regions. VFDT and CLOX2 did not show this common pattern and correlated with more limited medial occipito-temporal and occipito-parietal regions. Performance in all visuospatial/visuoperceptual tests correlated with fractional anisotropy in the corpus callosum. Conclusions: Our findings show that JLOT, SDMT, and PCT, in addition to differentiating patients from controls, are suitable visuospatial/visuoperceptual tests to reflect cortical thinning in lateral temporo-parietal regions in PD patients. We did not observe the dissociation between dorsal and ventral streams that was expected according to the neuropsychological classification of visuospatial and visuoperceptual tests. (JINS, 2018, 24, 33–44)
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Changing the line orientation in the MMN task is a process known to involve specific parietal regions.
“changing the line orientation in our MMN task is a process known to involve specific parietal regions34”
From Deviations in effective connectivity explain different hallucination subtypes in Parkinson's disease psychosis (2026) · cites this paper as [34]
The Results (page not provided) link performance on the Judgment of Line Orientation Test to cortical thickness in specific parietal regions, including the precuneus and supramarginal gyrus, in patients with Parkinson’s disease. The paper does not study changing a line’s orientation in an MMN task, and a structural correlation does not establish that those regions are involved in that process. (LLM, conf=0.86)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Desikan, R. S., Ségonne, F., Fischl, B., Quinn, B. T., Dickerson, B. C., Blacker, D., Buckner, R. L., Dale, A. M., Maguire, R. P., Hyman, B. T., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.01.021 · Cited by 13,324 · see citing works
Fast robust automated brain extraction
Smith, S. M. (2002) · Human Brain Mapping · doi:10.1002/hbm.10062 · Cited by 10,496 · see citing works
Tract-based spatial statistics: Voxelwise analysis of multi-subject diffusion data
Smith, S. M., Jenkinson, M., Johansen-Berg, H., Rueckert, D., Nichols, T. E., Mackay, C., Watkins, K., Ciccarelli, O., Cader, M., Matthews, P., et al. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.02.024 · Cited by 6,035 · see citing works
Systematic review of levodopa dose equivalency reporting in Parkinson's disease
Tomlinson, C. L., Stowe, R. L., Patel, S., Rick, C., Gray, R. G., & Clarke, C. E. (2010) · Movement Disorders · doi:10.1002/mds.23429 · Cited by 4,219 · see citing works
Distributed and overlapping representations of faces and objects in ventral temporal cortex
Haxby, J. V., Gobbini, M. I., Furey, M. L., Ishai, A., Schouten, J. L., & Pietrini, P. (2001) · Science · doi:10.1126/science.1063736 · Cited by 3,940 · see citing works
Object vision and spatial vision: Two cortical pathways
Mishkin, M., Ungerleider, L. G., & Macko, K. A. (1983) · Trends in Neurosciences · doi:10.1016/0166-2236(83)90190-x · Cited by 2,947 · see citing works
Litvan, I., Goldman, J. G., Tröster, A. I., Schmand, B. A., Weintraub, D., Petersen, R. C., Mollenhauer, B., Adler, C. H., Marder, K., Williams‐Gray, C. H., et al. (2012) · Movement Disorders · doi:10.1002/mds.24893 · Cited by 2,609 · see citing works
Recent developments in Parkinson's disease
Fahn, S., Elton, R., MARSDEN, C. D., Calne, D. B., & Goldstein, M. (1986) · Raven Press eBooks · Cited by 2,306 · see citing works
Recent Developments in Parkinson's Disease
Hurtig, H. I. (1987) · Neurology · doi:10.1212/wnl.37.5.893 · Cited by 1,926 · see citing works
Prevalence and Characteristics of Dementia in Parkinson Disease
Aarsland, D., Andersen, K., Larsen, J. O., & Lolk, A. (2003) · Archives of Neurology · doi:10.1001/archneur.60.3.387 · Cited by 1,403 · see citing works
A new neural framework for visuospatial processing
Kravitz, D. J., Saleem, K. S., Baker, C. I., & Mishkin, M. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn3008 · Cited by 1,325 · see citing works
Dubois, B., Burn, D. J., Goetz, C. G., Aarsland, D., Brown, R. G., Broe, G. A., Dickson, D. W., Duyckaerts, C. J., Cummings, J., Gauthier, S. G., et al. (2007) · Movement Disorders · doi:10.1002/mds.21844 · Cited by 1,069 · see citing works
Hely, M. A., Morris, J. G. L., Reid, W. G. J., & Trafficante, R. (2005) · Movement Disorders · doi:10.1002/mds.20324 · Cited by 1,050 · see citing works
Dissociation of object and spatial visual processing pathways in human extrastriate cortex.
Haxby, J. V., Grady, C. L., Horwitz, B., Ungerleider, L. G., Mishkin, M., Carson, R. E., Herscovitch, P., Schapiro, M. B., & Rapoport, S. I. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.5.1621 · Cited by 1,041 · see citing works
The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort
Williams‐Gray, C. H., Evans, J., Goris, A., Foltynie, T., Ban, M., Robbins, T. W., Brayne, C., Kolachana, B. S., Weinberger, D. R., Sawcer, S. J., et al. (2009) · Brain · doi:10.1093/brain/awp245 · Cited by 970 · see citing works
Evolution of cognitive dysfunction in an incident Parkinson's disease cohort
Williams‐Gray, C. H., Foltynie, T., Brayne, C., Robbins, T. W., & Barker, R. (2007) · Brain · doi:10.1093/brain/awm111 · Cited by 935 · see citing works
CLOX: an executive clock drawing task
Royall, D. R., Cordes, J. A., & Polk, M. J. (1998) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.64.5.588 · Cited by 839 · see citing works
Twenty‐five pitfalls in the analysis of diffusion MRI data
Jones, D. K., & Cercignani, M. (2010) · NMR in Biomedicine · doi:10.1002/nbm.1543 · Cited by 827 · see citing works
Smoothing and cluster thresholding for cortical surface-based group analysis of fMRI data
Hagler, D. J., Saygin, A. P., & Sereno, M. I. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.07.036 · Cited by 752 · see citing works
The CamPaIGN study of Parkinson's disease: 10-year outlook in an incident population-based cohort
Williams‐Gray, C. H., Mason, S., Evans, J., Foltynie, T., Brayne, C., Robbins, T. W., & Barker, R. A. (2013) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2013-305277 · Cited by 683 · see citing works
Cognitive impairment in incident, untreated Parkinson disease: The Norwegian ParkWest Study
Aarsland, D., Brønnick, K., Larsen, J. P., Tysnes, O. B., & Alves, G. (2009) · Neurology · doi:10.1212/01.wnl.0000338632.00552.cb · Cited by 625 · see citing works
Parkinson's Disease Society Brain Bank, London: overview and research.
Daniel, S. E., & Lees, A. J. (1993) · PubMed · Cited by 598 · see citing works
Visual dysfunction in Parkinson’s disease
Weil, R. S., Schrag, A. E., Warren, J. D., Crutch, S. J., Lees, A. J., & Morris, H. R. (2016) · Brain · doi:10.1093/brain/aww175 · Cited by 481 · see citing works
(2013) · David Fulton Publishers eBooks · doi:10.4324/9780203390269-11 · Cited by 478 · see citing works
Methodological considerations on tract-based spatial statistics (TBSS)
Bach, M., Laun, F. B., Leemans, A., Tax, C. M. W., Biessels, G. J., Stieltjes, B., & Maier-Hein, K. H. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.06.021 · Cited by 445 · see citing works
Cognitive impairment and resting-state network connectivity in Parkinson's disease
Baggio, H. C., Segura, B., Sala‐Llonch, R., Martı́, M. J., Valldeoriola, F., Compta, Y., TOLOSA, E. S., & Junqué, C. (2014) · Human Brain Mapping · doi:10.1002/hbm.22622 · Cited by 316 · see citing works
Self-citationVisuospatial impairment in Parkinson's disease
Levin, B. E., Llabre, M. M., Reisman, S. S., Weiner, W. J., Sanchez‐Ramos, J., Singer, C., & Brown, M. C. (1991) · Neurology · doi:10.1212/wnl.41.3.365 · Cited by 290 · see citing works
Functional brain networks and cognitive deficits in Parkinson's disease
Baggio, H. C., Sala‐Llonch, R., Segura, B., Martı́, M. J., Valldeoriola, F., Compta, Y., TOLOSA, E. S., & Junqué, C. (2014) · Human Brain Mapping · doi:10.1002/hbm.22499 · Cited by 246 · see citing works
Self-citationPereira, J. B., Ibarretxe‐Bilbao, N., Martı́, M. J., Compta, Y., Junqué, C., Bargalló, N., & TOLOSA, E. S. (2011) · Human Brain Mapping · doi:10.1002/hbm.21378 · Cited by 221 · see citing works
Self-citationCognitive status correlates with white matter alteration in Parkinson's disease
Hattori, T., Orimo, S., Aoki, S., Ito, K., Abe, O., Amano, A., Sato, R., Sakai, K., & Mizusawa, H. (2011) · Human Brain Mapping · doi:10.1002/hbm.21245 · Cited by 201 · see citing works
Schwarz, C., Reid, R. I., Gunter, J., Senjem, M., Przybelski, S., Zuk, S., Whitwell, J., Vemuri, P., Josephs, K., Kantarci, K., et al. (2014) · NeuroImage · doi:10.1016/j.neuroimage.2014.03.026 · Cited by 171 · see citing works
Oculo-Visual Dysfunction in Parkinson’s Disease
Armstrong, R. A. (2015) · Journal of Parkinson s Disease · doi:10.3233/jpd-150686 · Cited by 139 · see citing works
Pattern of Regional Cortical Thinning Associated with Cognitive Deterioration in Parkinson’s Disease
Pagonabarraga, J., Corcuera‐Solano, I., Vives‐Gilabert, Y., Llebaria, G., García‐Sánchez, C., Pascual‐Sedano, B., Delfino, M., Kulisevsky, J., & Gómez‐Ansón, B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054980 · Cited by 138 · see citing works
Clock Drawing Errors in Dementia
Cosentino, S., Jefferson, A. L., Chute, D. L., Kaplan, E., & Libon, D. J. (2004) · Cognitive and Behavioral Neurology · doi:10.1097/01.wnn.0000119564.08162.46 · Cited by 136 · see citing works
Neuroanatomical substrate of visuospatial and visuoperceptual impairment in Parkinson's disease
Pereira, J. B., Junqué, C., Martı́, M. J., Ramírez‐Ruiz, B., Bargalló, N., & TOLOSA, E. S. (2009) · Movement Disorders · doi:10.1002/mds.22560 · Cited by 135 · see citing works
Cortical thinning associated with mild cognitive impairment in Parkinson's disease
Segura, B., Baggio, H. C., Martı́, M. J., Valldeoriola, F., Compta, Y., García-Díaz, A. I., Vendrell, P., Bargalló, N., TOLOSA, E. S., & Junqué, C. (2014) · Movement Disorders · doi:10.1002/mds.25982 · Cited by 124 · see citing works
Self-citationCognitive Changes in Parkinson’s Disease Patients with Visual Hallucinations
Ramírez‐Ruiz, B., Junqué, C., Martı́, M. J., Valldeoriola, F., & TOLOSA, E. S. (2007) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000100850 · Cited by 104 · see citing works
Self-citationThe visual corticostriatal loop through the tail of the caudate: circuitry and function
Seger, C. A. (2013) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2013.00104 · Cited by 95 · see citing works
Zalesky, A. (2011) · Magnetic Resonance Imaging · doi:10.1016/j.mri.2010.06.027 · Cited by 88 · see citing works
A Symbol Digit Modalities Test version suitable for functional MRI studies
Forn, C., Belloch, V., Bustamante, J. C., et al. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.081 · Cited by 72 · see citing works
Volumetric correlates of cognitive functioning in nondemented patients with Parkinson's disease
Filoteo, J. V., Reed, J. D., Litvan, I., & Harrington, D. L. (2013) · Movement Disorders · doi:10.1002/mds.25633 · Cited by 63 · see citing works
A studyforrest extension, retinotopic mapping and localization of higher visual areas
Sengupta, A., Kaule, F. R., Guntupalli, J. S., Hoffmann, M. B., Häusler, C. O., Stadler, J., & Hanke, M. (2016) · Scientific Data · doi:10.1038/sdata.2016.93 · Cited by 63 · see citing works
Structural MRI correlates of the MMSE and pentagon copying test in Parkinson's disease
García-Díaz, A. I., Segura, B., Baggio, H. C., Martı́, M. J., Valldeoriola, F., Compta, Y., Vendrell, P., Bargalló, N., TOLOSA, E. S., & Junqué, C. (2014) · Parkinsonism & Related Disorders · doi:10.1016/j.parkreldis.2014.10.014 · Cited by 39 · see citing works
Self-citationForti, P., Olivelli, V., Rietti, E., Maltoni, B., & Ravaglia, G. (2010) · Dementia and Geriatric Cognitive Disorders · doi:10.1159/000315515 · Cited by 29 · see citing works
Deng, Y., Shi, L., Yi, L., Liang, P., Li, K., Chu, C. W., & Wang, D. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00333 · Cited by 27 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Vignando, M., Ffytche, D., Mazibuko, N., Palma, G., Bhat, A., Montagnese, M., Dave, S., Tai, Y. F., Batzu, L., Leta, V., et al. (2026) · Nature Mental Health · doi:10.1038/s44220-026-00669-7
“…strong results for the dorsal pathway in the source reconstruction analysis we focused on one dorsal model, using source reconstruction results, and the literature on the Benton line judgment task and the neural anatomy of the dorsal pathway 34 to define the dipoles (Supplementary Information 11).”
- Authors
- Garcia-Diaz, A. I., Segura, B., Baggio, H. C., Marti, M. J., Valldeoriola, F., Compta, Y., Bargallo, N., Uribe, C., Campabadal, A., Abos, A., & Junque, C.
- Affiliations
- Biomedical Research Networking Center on Neurodegenerative Diseases (ES)
- Universitat de Barcelona (ES)
- Consorci Institut D'Investigacions Biomediques August Pi I Sunyer (ES)
- Venue
- Journal of the International Neuropsychological Society
- Publisher
- Cambridge University Press (CUP)
- Published
- 2017-07-17
- Volume
- 24
- Issue
- 1
- Pages
- 33-44
- ISSN
- 1355-6177 (ISSN-L)
- 1469-7661
- PMC
- PMC5851059
- OpenAlex
- W2734826538
- Cited by
- 39
- References
- 45
- Citations by year
- 2026: 4 · 2025: 3 · 2024: 5 · 2023: 4 · 2022: 7 · 2021: 3 · 2020: 4 · 2019: 5 · 2018: 3 · 2017: 1
- FWCI
- 2.47
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Journal of the International Neuropsychological Society (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Dipòsit Digital de la Universitat de Barcelona (Universitat de Barcelona) (publishedVersion)
- Funders
- Fundació la Marató de TV3 (20142310)
- Generalitat de Catalunya (2014 SGR 98, 20142310, 2014SGR)
- Ministerio de Economía y Competitividad (PSI2013-41393-P, BES-2014-068173)
- European Social Fund (PSI2013-41393-P)
- Topics
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Social Sciences › Psychology › Clinical Psychology › Historical and Modern Theater Studies
- Keywords
- Parkinson's disease, mild cognitive impairment, neuroanatomical correlates, cortical thickness, fractional anisotropy, corpus callosum, temporoparietal cortex, dorsal and ventral visual streams, Symbol Digit Modalities Test, face recognition (cognition)
- MeSH terms
- Aged, Cerebral Cortex, Female, Humans, Male, Middle Aged, Neuropsychological Tests, Parkinson Disease, Space Perception, Visual Perception, Cohort Studies, Diffusion Tensor Imaging, Cognitive Dysfunction
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review