Single-Subject Grey Matter Graphs in Alzheimer's Disease
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Coordinated patterns of cortical morphology have been described as structural graphs and previous research has demonstrated that properties of such graphs are altered in Alzheimer's disease (AD). However, it remains unknown how these alterations are related to cognitive deficits in individuals, as such graphs are restricted to group-level analysis. In the present study we investigated this question in single-subject grey matter networks. This new method extracts large-scale structural graphs where nodes represent small cortical regions that are connected by edges when they show statistical similarity. Using this method, unweighted and undirected networks were extracted from T1 weighted structural magnetic resonance imaging scans of 38 AD patients (19 female, average age 72±4 years) and 38 controls (19 females, average age 72±4 years). Group comparisons of standard graph properties were performed after correcting for grey matter volumetric measurements and were correlated to scores of general cognitive functioning. AD networks were characterised by a more random topology as indicated by a decreased small world coefficient (p = 3.53×10(-5)), decreased normalized clustering coefficient (p = 7.25×10(-6)) and decreased normalized path length (p = 1.91×10(-7)). Reduced normalized path length explained significantly (p = 0.004) more variance in measurements of general cognitive decline (32%) in comparison to volumetric measurements (9%). Altered path length of the parahippocampal gyrus, hippocampus, fusiform gyrus and precuneus showed the strongest relationship with cognitive decline. The present results suggest that single-subject grey matter graphs provide a concise quantification of cortical structure that has clinical value, which might be of particular importance for disease prognosis. These findings contribute to a better understanding of structural alterations and cognitive dysfunction in AD.
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Some studies have observed conflicting results, including lower characteristic path length in DTI, gray matter, fMRI, EEG, and MEG connectomes in patients with AD.
“However, some studies have observed conflicting results, including lower characteristic path length in DTI (Daianu et al., 2013), gray matter (Tijms, Moller et al., 2013), fMRI (Sanz-Arigita et al., 2010), EEG (de Haan et al., 2009), and magneto-encephalogram (MEG; Stam et al., 2009) connectomes in patients with AD.”
From Functional and structural connectome properties in the 5XFAD transgenic mouse model of Alzheimer’s disease (2018) · cites this paper as Tijms, Moller et al., 2013
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Gaiteri, C., Mostafavi, S., Honey, C. J., Jager, P. L. D., & Bennett, D. A. (2016) · Nature Reviews Neurology · doi:10.1038/nrneurol.2016.84 · Cited by 96 · see citing works
Reduced integration and improved segregation of functional brain networks in Alzheimer’s disease
Kabbara, A., Eid, H., Falou, W. E., Khalil, M. A., Wendling, F., & Hassan, M. (2018) · Journal of Neural Engineering · doi:10.1088/1741-2552/aaaa76 · Cited by 89 · see citing works
Phillips, D. J., McGlaughlin, A., Ruth, D. M., Jager, L. R., & Soldan, A. (2015) · NeuroImage Clinical · doi:10.1016/j.nicl.2015.01.007 · Cited by 89 · see citing works
“…of disease severity (Heet al., 2008; Yaoet al., 2010; Zhaoet al., 2012),others have reported a decrease (Li et al., 2012; Stam et al., 2009; Sun et al., 2014; Tijms et al., 2013a) and still others found no difference (Bai et al., 2012; Lo et al., 2010; Sanz-Arigita et al., 2010; Stam et al., 2007).”
BackgroundMethodResultInfluentialIndividual‐level brain morphological similarity networks: Current methodologies and applications
Cai, M., Ma, J., Wang, Z., Zhao, Y., Zhang, Y., Wang, H., Xue, H., Chen, Y., Zhang, Y., Wang, C., et al. (2023) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.14384 · Cited by 77 · see citing works
“47,48 The morphological similarity measurement can better reveal cortical structural changes and impairments in memory as well as cognition in patients with AD.”
BackgroundMak, E., Gabel, S., Mirette, H., Su, L., Williams, G. B., Waldman, A., Wells, K., Ritchie, K., Ritchie, C., & O’Brien, J. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2016.10.001 · Cited by 71 · see citing works
“In contrast, others have reported decrease clustering in AD (Tijms et al., 2013a).”
Batallé, D., Muñoz‐Moreno, E., Figueras, F., Bargalló, N., Eixarch, E., & Gratacós, E. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.07.045 · Cited by 74 · see citing works
“Recently, a number of published reports have suggested approaches to extract individual brain networks based on the analysis of the similarities of GM features (Raj et al., 2010; Tijms et al., 2012, 2013; Zhou et al., 2011).”
BackgroundAltered topology of the functional speech production network in non-fluent/agrammatic variant of PPA
Mandelli, M. L., Welch, A. E., Vilaplana, E., Watson, C., Battistella, G., Brown, J. A., Possin, K. L., Hubbard, H. I., Miller, Z. A., Henry, M. L., et al. (2018) · Cortex · doi:10.1016/j.cortex.2018.08.002 · Cited by 67 · see citing works
Zheng, W., Yao, Z., Xie, Y., Fan, J., & Hu, B. (2018) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2018.06.004 · Cited by 59 · see citing works
Tijms, B. M., Yeung, H. M., Sikkes, S. A. M., Möller, C., Smits, L. L., Stam, C. J., Scheltens, P., van der Flier, W. M., & Barkhof, F. (2014) · Brain Connectivity · doi:10.1089/brain.2013.0209 · Cited by 65 · see citing works
Self-citationGray matter networks and clinical progression in subjects with predementia Alzheimer's disease.
Tijms, B., ten Kate, M., Gouw, A., Borta, A., Verfaillie, S., Teunissen, C., Scheltens, P., Barkhof, F., & van der Flier, W. M. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.09.011 · Cited by 62 · see citing works
“We previously have shown that worse grey matter network disruptions are associated with worse disease severity and cognitive dysfunction [20,21].”
Self-citationStability of graph theoretical measures in structural brain networks in Alzheimer’s disease
Mårtensson, G., Pereira, J. B., Mecocci, P., Vellas, B., Tsolaki, M., Kłoszewska, I., Soininen, H., Lovestone, S., Simmons, A., Volpe, G., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-29927-0 · Cited by 60 · see citing works
Gray matter network disruptions and amyloid beta in cognitively normal adults
Tijms, B. M., Kate, M. T., Wink, A. M., Visser, P. J., Ecay, M., Clerigue, M., Estanga, A., Garcia Sebastian, M., Izagirre, A., Villanua, J., et al. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2015.10.015 · Cited by 59 · see citing works
Self-citationBrain gray matter network organization in psychotic disorders
Zhang, W., Lei, D., Keedy, S., Ivleva, E. I., Eum, S., Li, Y., Tamminga, C. A., Clementz, B. A., Keshavan, M. S., Pearlson, G. D., et al. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0586-2 · Cited by 56 · see citing works
Hafkemeijer, A., Möller, C., Dopper, E. G. P., Jiskoot, L. C., van den Berg‐Huysmans, A. A., Swieten, J. C. V., van der Flier, W. M., Vrenken, H., Pijnenburg, Y. A. L., Barkhof, F., et al. (2015) · Human Brain Mapping · doi:10.1002/hbm.23081 · Cited by 56 · see citing works
“Our findings are in line with the observations of decreased network integrity [Montembeault et al., 2015; Spreng and Turner, 2013; Tijms et al., 2013] and cortical shrinking [He et al., 2008; Reid and Evans, 2013] in this network in AD compared with controls.”
ResultSelf-citationChen, T., Kendrick, K. M., Wang, J., Wu, M. C., Li, K., Huang, X., Luo, Y., Lui, S., Sweeney, J. A., & Gong, Q. (2017) · Human Brain Mapping · doi:10.1002/hbm.23534 · Cited by 59 · see citing works
“Second, while the construction of similarity-based individual structural networks has been successfully applied to other neuropsychiatric disorders [Tijms et al., 2013, 2014], the biological significance of these network alterations needs to be more fully understood.”
BackgroundMethodGray matter networks and cognitive impairment in multiple sclerosis
Rimkus, C., Schoonheim, M., Steenwijk, M., Vrenken, H., Eijlers, A., Killestein, J., Wattjes, M., Leite, C., Barkhof, F., & Tijms, B. (2018) · Multiple Sclerosis · doi:10.1177/1352458517751650 · Cited by 50 · see citing works
“10,11 The first gray matter network studies in MS based on cortical thickness inter-regional correlation analysis have demonstrated that gray matter networks become disorganized, 12,13 which seems to be associated with white matter lesion load 12 and disrupted functional connectivity.”
Self-citationDisruption of Resting Functional Connectivity in Alzheimer’s Patients and At-Risk Subjects
Krajčovičová, L., Mareček, R., Mikl, M., & Rektorová, I. (2014) · Current Neurology and Neuroscience Reports · doi:10.1007/s11910-014-0491-3 · Cited by 51 · see citing works
Verfaillie, S., Slot, R. E., Dicks, E., Prins, N., Overbeek, J. M., Teunissen, C., Scheltens, P., Barkhof, F., van der Flier, W. M., & Tijms, B. (2018) · Human Brain Mapping · doi:10.1002/hbm.24065 · Cited by 43 · see citing works
Self-citationNovel Cortical Thickness Pattern for Accurate Detection of Alzheimer’s Disease
Zheng, W., Yao, Z., Hu, B., Gao, X., Cai, H., Moore, P. T., & Initiative, A. F. T. A. D. N. (2015) · Journal of Alzheimer s Disease · doi:10.3233/jad-150311 · Cited by 42 · see citing works
Vignando, M., ffytche, D., Lewis, S. J. G., Lee, P. H., Chung, S. J., Weil, R. S., Hu, M. T., Mackay, C. E., Griffanti, L., Pins, D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-28087-0 · Cited by 42 · see citing works
Beheshti, I., Maikusa, N., Matsuda, H., Demirel, H., & Anbarjafari, G. (2016) · Journal of Alzheimer's Disease · doi:10.3233/jad-160850 · Cited by 42 · see citing works
Gray Matter Network Disruptions and Regional Amyloid Beta in Cognitively Normal Adults
ten Kate, M., Visser, P. J., Bakardjian, H., Barkhof, F., Sikkes, S. A. M., van der Flier, W. M., Scheltens, P., Hampel, H., Habert, M.-O., Dubois, B., et al. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00067 · Cited by 41 · see citing works
Self-citationMultiplex Networks for Early Diagnosis of Alzheimer's Disease
Amoroso, N., Rocca, M. L., Bruno, S., Maggipinto, T., Monaco, A., Bellotti, R., & Tangaro, S. (2018) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2018.00365 · Cited by 56 · see citing works
Grey matter networks in people at increased familial risk for schizophrenia
Tijms, B. M., Sprooten, E., Job, D. E., Johnstone, E. C., Owens, D. G. C., Willshaw, D. J., Seriès, P., & Lawrie, S. M. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2015.08.025 · Cited by 40 · see citing works
“Wehave previously demonstrated that an a priori difference in the amount inweak connections can influence other network property values, even if the connectivity density is identical (Tijms et al., 2013).”
BackgroundSelf-citationFujii, H., Sato, W., Kimura, Y., Matsuda, H., Ota, M., Maikusa, N., Suzuki, F., Amano, K., Shin, I., Yamamura, T., et al. (2020) · Journal of Neuroimaging · doi:10.1111/jon.12751 · Cited by 35
Kesler, S. R., Acton, P., Rao, V., & Ray, W. J. (2018) · Network Neuroscience · doi:10.1162/netn_a_00048 · Cited by 34 · see citing works
Altered Network Topology in Patients with Primary Brain Tumors After Fractionated Radiotherapy
Bahrami, N., Seibert, T. M., Karunamuni, R. A., Bartsch, H., Krishnan, A. P., Farid, N., Hattangadi-Gluth, J. A., & McDonald, C. R. (2017) · Brain Connectivity · doi:10.1089/brain.2017.0494 · Cited by 34 · see citing works
“…that RT may result in damage to vascular endothelial cells and to the hippocampus (Kim et al., 2004; Seibert et al., 2017), studies that have applied graph theory to examine cortical networks in patients with AD may serve as good models (He et al., 2008; Pereira et al., 2016; Tijms et al., 2013b).”
BackgroundInfluentialA Graph Theory Approach to Clarifying Aging and Disease Related Changes in Cognitive Networks
Wright, L. M., Marco, M. D., & Venneri, A. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.676618 · Cited by 32 · see citing works
Structural covariance analysis for neurodegenerative and neuroinflammatory brain disorders
Mongay‐Ochoa, N., González‐Escamilla, G., Fleischer, V., Pareto, D., Rovira, À., Sastre‐Garriga, J., & Groppa, S. (2025) · Brain · doi:10.1093/brain/awaf151 · Cited by 29 · see citing works
“Patients with a more severe cognitive impairment have been shown to display more random graph-based morphometric properties, 41 as indicated by correlations between the average path length, clustering coefficient and the Mini-Mental State Examination (MMSE) scores, particularly evident in the left…”
Influentialvan Duinkerken, E., IJzerman, R. G., Klein, M., Moll, A. C., Snoek, F. J., Scheltens, P., Pouwels, P. J. W., Barkhof, F., Diamant, M., & Tijms, B. M. (2015) · Human Brain Mapping · doi:10.1002/hbm.23096 · Cited by 28 · see citing works
“This is similar to our previous research also showing that using 20 random reference graphs is sufficient to obtain stable network statistics [Tijms et al., 2013].”
BackgroundResultSelf-citationWatson, C. G., Stopp, C. D., Newburger, J. W., & Rivkin, M. J. (2018) · Brain and Behavior · doi:10.1002/brb3.834 · Cited by 30 · see citing works
“A vertex was considered to be a hub if its betweenness centrality was at least one standard deviation greater than the mean across all vertices for that density (Bernhardt et al., 2011; Hosseini et al., 2013; Tijms et al., 2013; Wang et al., 2013).”
BackgroundAlzhemimer’s Disease is Characterized by Lower Segregation in Resting-State Eyes-Closed EEG
AYDIN, S. (2024) · Journal of Medical and Biological Engineering · doi:10.1007/s40846-024-00917-0 · Cited by 28 · see citing works
“However, the following studies did not find group differences in global connectivity between AD and controls with respect to resting-state fMRI data [15, 49].”
Divergent topological networks in Alzheimer’s disease: a diffusion kurtosis imaging analysis
Cheng, J.-X., Zhang, H., Peng, Z.-K., Xu, Y. Q., Tang, H., Wu, J., & Xu, J. L. (2018) · Translational Neurodegeneration · doi:10.1186/s40035-018-0115-y · Cited by 26 · see citing works
“On the contrary, decreased Lp in AD was also demonstrated by using sMRI and DTI [17, 54].”
MethodDisrupted grey matter network morphology in pediatric posttraumatic stress disorder
Niu, R., Lei, D., Chen, F., Chen, Y., Suo, X., Li, L., Lui, S., Huang, X., Sweeney, J. A., & Gong, Q. (2018) · NeuroImage Clinical · doi:10.1016/j.nicl.2018.03.030 · Cited by 35 · see citing works
Dyrba, M., Mohammadi, R., Grothe, M. J., Kirste, T., & Teipel, S. J. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00099 · Cited by 47 · see citing works
Reduced local segregation of single‐subject gray matter networks in adult PTSD
Niu, R., Lei, D., Chen, F., Chen, Y., Suo, X., Li, L., Lui, S., Huang, X., Sweeney, J. A., & Gong, Q. (2018) · Human Brain Mapping · doi:10.1002/hbm.24330 · Cited by 26 · see citing works
Tau-related grey matter network breakdown across the Alzheimer’s disease continuum
Pelkmans, W., Ossenkoppele, R., Dicks, E., Strandberg, O. T., Barkhof, F., Tijms, B. M., Pereira, J. B., & Hansson, O. (2021) · Alzheimer s Research & Therapy · doi:10.1186/s13195-021-00876-7 · Cited by 25 · see citing works
“In AD dementia patients nearly all network metrics were abnormal, suggesting that with pronounced neurodegeneration GM networks exhibit significant topological alterations, which is in line with previous studies in AD dementia [18, 22, 23].”
ResultSelf-citationStructural cortical network reorganization associated with early conversion to multiple sclerosis
Tur, C., Eshaghi, A., Altmann, D. R., Jenkins, T. M., Prados, F., Grussu, F., Charalambous, T., Schmidt, A., Sebastien Ourselin, A., Clayden, J. D., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-29017-1 · Cited by 24 · see citing works
Brain Structural Covariance Network Topology in Remitted Posttraumatic Stress Disorder
Sun, D., Davis, S. L., Haswell, C. C., Swanson, C. A., Workgroup, M.-A. M., LaBar, K. S., Fairbank, J. A., & Morey, R. A. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00090 · Cited by 22 · see citing works
“An single-subject gray matter graph method has been developed in recent years (78, 79) and should be utilized in future studies of PTSD and remission.”
MethodJiang, J.-H., Zhou, H., Duan, H.-Q., Liu, X., Zuo, C.-T., Huang, Z., Yu, Z., & Yan, Z. (2017) · Heliyon · doi:10.1016/j.heliyon.2017.e00475 · Cited by 23 · see citing works
“A decrease clustering in the AD group could also be found [39, 40], etc.”
BackgroundCoronary Heart Disease and Cortical Thickness, Gray Matter and White Matter Lesion Volumes on MRI
Vuorinen, M., Damangir, S., Niskanen, E. I., Miralbell, J., Rusanen, M., Spulber, G., Soininen, H. S., Kivipelto, M., & Solomon, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109250 · Cited by 20 · see citing works
Rozhkov, A. (2024) · Applied Energy · doi:10.1016/j.apenergy.2024.122854 · Cited by 25 · see citing works
Wang, X., Cui, X.-H., Ding, C., Li, D.-D., Cheng, C., Wang, B., & Xiang, J. (2020) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.27453 · Cited by 21 · see citing works
“However, hubs are also the weakest links in the network.(33) Studies have shown that hubs in the network may be selectively vulnerable in AD patients.”
BackgroundDicks, E., van der Flier, W. M., Scheltens, P., Barkhof, F., & Tijms, B. (2020) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2020.05.008 · Cited by 21 · see citing works
“We and others have shown that gray matter networks are disrupted in AD (He et al., 2008; Pereira et al., 2016; Tijms et al., 2013a,b; Yao et al., 2010), associated with cognitive impairment (Tijms et al., 2013a, 2014), and related to faster disease progression and cognitive decline in the…”
Self-citationBrain structural connectivity atrophy in Alzheimer's diseasePreprint
Amoroso, N., Rocca, M. L., Bruno, S., Maggipinto, T., Monaco, A., Bellotti, R., & Tangaro, S. (2017) · arXiv (Cornell University) · doi:10.48550/arxiv.1709.02369 · Cited by 13 · see citing works
“Several studies have already pointed out, especially with group-wise single layer approaches 51 , how these features can describe significant differences among healthy and diseased subjects.”
BackgroundDisrupted brain gray matter networks in drug-naïve participants with essential tremor
Yang, J., Lei, D., Peng, J., Suo, X., Pinaya, W. H. L., Li, W., Li, J., Kemp, G. J., Peng, R., & Gong, Q. (2021) · Neuroradiology · doi:10.1007/s00234-021-02653-7 · Cited by 21 · see citing works
Hypermetabolic Cerebellar Connectome in Alzheimer's Disease
Gupta, V., Booth, S., & Ko, J. (2020) · Brain Connectivity · doi:10.1089/brain.2020.0937 · Cited by 20 · see citing works
“…of short path length and high clustering in the AD network suggests an evolutionary optimization of the equilibrium between information segregation (represented by nodes forming particular clusters) and information integration (represented by interactions among clusters; Tijms et al., 2013a).”
Multivariate regression analysis of structural MRI connectivity matrices in Alzheimer’s disease
Rasero, J., Amoroso, N., Rocca, M. L., Tangaro, S., Bellotti, R., Stramaglia, S., & Initiative, A. D. N. (2017) · PLoS ONE · doi:10.1371/journal.pone.0187281 · Cited by 18 · see citing works
Vermunt, L., Dicks, E., Wang, G., Dincer, A., Flores, S. E., Keefe, S., Berman, S. B., Cash, D. M., Chhatwal, J. P., Cruchaga, C., et al. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa102 · Cited by 21 · see citing works
Self-citationZheng, W., Yao, Z., Li, Y., Zhang, Y., Hu, B., Wu, D., & Initiative, A. D. N. (2019) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2019.00399 · Cited by 19 · see citing works
Wang, B., Miao, L., Niu, Y., Cao, R., Li, D., Yan, P., Guo, H., Yan, T., Wu, J., Xiang, J., et al. (2018) · Journal of Alzheimer s Disease · doi:10.3233/jad-180603 · Cited by 22 · see citing works
The Brain Network Hub Degeneration in Alzheimer’s Disease
Jin, S., Wang, J., & Yong He, A. (2024) · Biophysics Reports · doi:10.52601/bpr.2024.230025 · Cited by 11 · see citing works
“Specifically, using a cube-based correlation method for single-subject morphological brain networks, Tijms and colleagues found AD-related betweenness decreases in the posterior cingulate gyrus, parahippocampal gyrus, lingual gyrus, and bilateral thalamus (Tijms et al. 2013a).”
MethodResultGrey matter network trajectories across the Alzheimer’s disease continuum and relation to cognition
Dicks, E., Vermunt, L., van der Flier, W. M., Barkhof, F., Scheltens, P., Tijms, B. M., & Initiative, A. D. N. (2020) · Brain Communications · doi:10.1093/braincomms/fcaa177 · Cited by 20 · see citing works
Self-citationAltered structural connectivity networks in dementia with lewy bodies
Nicastro, N., Mak, E., Surendranathan, A., Rittman, T., Rowe, J., & O'Brien, J. (2021) · Brain Imaging and Behavior · doi:10.1007/s11682-020-00444-x · Cited by 17 · see citing works
Single-subject structural cortical networks in clinically isolated syndrome
Collorone, S., Prados, F., Hagens, M., Tur, C., Kanber, B., Sudre, C., Lukas, C., Gasperini, C., Oreja-Guevara, C., Andelova, M., et al. (2020) · Multiple Sclerosis · doi:10.1177/1352458519865739 · Cited by 17
Self-citationVignando, M., Ffytche, D., Lewis, S., Lee, P., Chung, S., Weil, R., Hu, M., Mackay, C., Griffanti, L., Pins, D., et al. (2021) · medRxiv · doi:10.1101/2021.02.17.21251558 · Cited by 16
“A hub was categorised as such if its betweenness centrality was greater than the mean plus 1 standard deviation - calculated on all vertices at the same density (e.g. Bernhardt et al., 2011; Hosseini et al., 2013; Tijms et al., 2013; Wang et al., 2013; Watson et al., 2018).”
BackgroundHawkins, R., Shatil, A. S., Lee, L., Sengupta, A., Zhang, L., Morrow, S., & Aviv, R. (2020) · American Journal of Neuroradiology · doi:10.3174/ajnr.a6435 · Cited by 16 · see citing works
“Reduction in l is indicative of a more random network and mirrors prior findings in MS, mild cognitive impairment, and Alzheimer disease.(13,23,24) Our results reinforce the link between reduced white matter integrity and impairment, particularly in executive functioning and processing speed.”
Noroozıan, M. (2015) · Neurologic Clinics · doi:10.1016/j.ncl.2015.08.005 · Cited by 16 · see citing works
Li, W., Wang, M.-D., Zhu, W.-Z., Qin, Y.-Y., Huang, Y., & Chen, X. (2016) · Scientific Reports · doi:10.1038/srep34156 · Cited by 15 · see citing works
Quantifying uncertainty in brain network measures using Bayesian connectomics
Janssen, R. J., Hinne, M., Heskes, T., & van Gerven, M. A. J. (2014) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2014.00126 · Cited by 11 · see citing works
Wang, Y.-Q., Li, J.-L., Jin, S.-H., Wang, J., Lv, Y.-T., Zou, Q.-H., & Wang, J.-H. (2024) · NeuroImage · doi:10.1016/j.neuroimage.2024.120673 · Cited by 14 · see citing works
“…have shown that various brain disorders were associated with anomalous topological organization for 1D-PD MCNs, such as Alzheimer ’ s disease (Tijms et al., 2013, 2014), multiple sclerosis (Fleischer et al., 2023; Yang et al., 2023), and depression (Chen et al., 2017; Han et al., 2023; Qiu…”
Tau trajectory in Alzheimer’s disease: Evidence from the connectome-based computational models
Bitra, V. R., Challa, S. R., Adiukwu, P. C., & Rapaka, D. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.110777 · Cited by 14 · see citing works
Li, W., Yang, C.-L., Wu, S.-C., Nie, Y.-N., Zhang, X., Lu, M., Chu, T.-P., & Shi, F. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00927 · Cited by 14 · see citing works
Li, Q., Li, X., Wang, X., Li, Y., Li, K., Yu, Y., Yin, C., Li, S., & Han, Y. (2016) · Neural Plasticity · doi:10.1155/2016/3462309 · Cited by 20 · see citing works
“Previous studies have demonstrated that the cortical thickness and GM volume can be used as morphological descriptors to study the complex cortical networks, and networks based on the cortical thickness and GM volume followed the small-world properties [10–12, 43, 44].”
BackgroundDrenthen, G. S., Backes, W. H., Freeze, W. M., Jacobs, H. I. L., Verheggen, I. C. M., van Boxtel, M. P. J., Hoff, E. I., Verhey, F. R., & Jansen, J. F. A. (2022) · Journal of Alzheimer’s Disease · doi:10.3233/jad-220175 · Cited by 10 · see citing works
Oxtoby, N., Ferreira, F. S., Mihalik, A., Wu, T., Brudfors, M., Lin, H., Rau, A., Blumberg, S. B., Robu, M., Zor, C., et al. (2019) · ABCD-NP@MICCAI · doi:10.1007/978-3-030-31901-4_14 · Cited by 10 · see citing works
Cantero, J. L., Atienza, M., Sánchez‐Juan, P., Rodríguez‐Rodríguez, E., Vázquez‐Higuera, J. L., Pozueta, A., González‐Suárez, A., Vilaplana, E., Pegueroles, J., Montal, V., et al. (2017) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.12.010 · Cited by 11 · see citing works
Ding, H., Wang, Z.-H., Tang, Y., Wang, T., Qi, M., Dou, W.-Q., Qian, L., Gao, Y., Zhong, Q., Yang, X., et al. (2023) · Quantitative Imaging in Medicine and Surgery · doi:10.21037/qims-22-1373 · Cited by 9 · see citing works
“Moreover, an inter-individual level analysis was proposed recently, based on cortical similarities in gray matter morphology within single cases (19,21,29-34).”
InfluentialXiao, Y., Gao, L., Hu, Y., & Initiative, T. A. D. N. (2024) · Frontiers in Neuroscience · doi:10.3389/fnins.2024.1366761 · Cited by 10 · see citing works
“These findings are in line with previous structural (Tijms et al., 2013a; Sheng et al., 2021; Ng et al., 2022) and functional (Stam et al., 2009; Sanz-Arigita et al., 2010) network studies in AD.”
BackgroundResultChen, T.-Y., Zhu, J.-D., Tsai, S.-J., & Yang, A. C. (2024) · Alzheimer's Research & Therapy · doi:10.1186/s13195-024-01448-1 · Cited by 8 · see citing works
“Since research on individual-based structural networks is still developing, few studies have focused on the micro-scale patterns and investigated the single-subject networks in individuals with AD [48, 49].”
BackgroundAge and Sex-Related Effects on Single-Subject Gray Matter Networks in Healthy Participants
Yoko, S., Sato, N., Maikusa, N., Sone, D., Ota, M., Kimura, Y., Chiba, E., Okita, K., Yamao, T., Nakaya, M., et al. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13030419 · Cited by 8
“In Alzheimer’s disease, a typical age-related neurodegenerative disorder, gray matter networks are known to disrupt and move to random networks [11].”
BackgroundMethodYoko, S., Sone, D., Okita, K., Maikusa, N., Yamao, T., Kimura, Y., Suzuki, F., Fujii, H., Kato, K., Sato, N., et al. (2021) · eNeurologicalSci · doi:10.1016/j.ensci.2021.100309 · Cited by 8 · see citing works
Ruiz-Gómez, S. J., Hornero, R., Poza, J., Santamaría-Vázquez, E., Rodríguez-González, V., Maturana-Candelas, A., & Gómez, C. (2021) · Journal of Neural Engineering · doi:10.1088/1741-2552/abd82c · Cited by 8 · see citing works
“Some works that investigated the average clustering coefficient did not find differences between AD and control subjects [14–16], others found significant decreases in AD [12, 17] and other studies also found an increased clustering in AD [18–20].”
BackgroundResultCognitive Performance Deficits and Dysgraphia in Alzheimer’s Disease Patients
Onofri, E., Mercuri, M., Salesi, M., Ricciardi, M. R., & Archer, T. (2015) · Open Medicine Journal · doi:10.2174/1874220301501010006 · Cited by 3 · see citing works
“In Western industrial nations, Alzheimer’s disease (AD) represents the most common form of dementia [5, 6], approximately 80% of cases [7], occupying fourth place among the causes of death (after heart disease and circulatory disorders, cancer and cerebral hemorrhage); the secondary forms of dementia, such as vascular…”
BackgroundChen, H.-F., Xu, J.-X., Lv, W.-P., Hu, Z.-Q., Ke, Z.-H., Qin, R.-M., Chen, Y., & Xu, Y. (2023) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2023.110714 · Cited by 7 · see citing works
“The graph feature values in the parahippocampal gyrus, hippocampus, and precuneus had the highest correlations with cognitive decline in comparison with other brain regions (Tijms, 2013).”
Siddiqui, M., François, M., Rainey‐Smith, S. R., Martins, R. N., Masters, C. L., Ames, D. J., Rowe, C. C., Macaulay, L. S., Fenech, M. F., & Leifert, W. R. (2020) · Life · doi:10.3390/life10080141 · Cited by 8 · see citing works
Michelutti, M., Urso, D., Tafuri, B., Gnoni, V., Giugno, A., Zecca, C., Dell’Abate, M. T., Vilella, D., Manganotti, P., Blasi, R. D., et al. (2025) · Journal of Alzheimer s Disease · doi:10.1177/13872877251316794 · Cited by 7 · see citing works
“– 76 The latter demonstrated that, despite alterations of individual graph metrics and a tendency to randomization were documented by structural 74,75 and functional 76,77 covariance network analyses, such networks retained a general small-world organization, 74 – 77 as observed in our study.”
Altered Structural Brain Network Topology in Patients With Primary Craniocervical Dystonia
Wang, X., Hu, W.-H., Wang, H., Gao, D., Liu, Y.-Y., Zhang, X., Jiang, Y., Mo, J.-J., Meng, F.-G., Zhang, K., et al. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.763305 · Cited by 6
Ng, K., Qian, X., Ng, K. K., Ji, F., Rosa-Neto, P., Gauthier, S., Kandiah, N., & Zhou, J. (2022) · bioRxiv · doi:10.7554/elife.77745 · Cited by 6 · see citing works
“…networks by computing intracortical similarities in GM morphology ( Tijms et al., 2012 ) showed that single-subject GM graph properties were associated with individual differences of clinical progression in AD ( Tijms et al., 2018 ; Tijms et al., 2014 ; Vermunt et al., 2020 ; Tijms et al., 2013 ).”
BackgroundNetwork Analyses and Nervous System Disorders
Medaglia, J., & Bassett, D. (2017) · Oxford Research Encyclopedia of Neuroscience · doi:10.1093/acrefore/9780190264086.013.121 · Cited by 6 · see citing works
Individual-specific networks for prediction modelling – A scoping review of methods
Gregorich, M., Melograna, F., Sunqvist, M., Michiels, S., Steen, K. V., & Heinze, G. (2022) · BMC Medical Research Methodology · doi:10.1186/s12874-022-01544-6 · Cited by 6 · see citing works
“%) examined the normalized clustering coefficient and characteristic path length obtained by dividing the CC and CPL by the CC and CPL of multiple randomly generated networks [18, 20, 79, 81, 84, 88].”
Sanabria-Diaz, G., Démonet, J., Rodríguez-Herreros, B., Draganski, B., Kherif, F., & Melie-García, L. (2021) · NeuroImage: Clinical · doi:10.1016/j.nicl.2021.102799 · Cited by 5 · see citing works
Lazarou, I., Georgiadis, K., Nikolopoulos, S., Oikonomou, V. P., Tsolaki, A., Kompatsiaris, I. Y., Tsolaki, M., & Kugiumtzis, D. (2020) · Brain Sciences · doi:10.3390/brainsci10060392 · Cited by 33 · see citing works
The relationship between negative life events and cortical structural connectivity in adolescents
Sibilia, F., Jost-Mousseau, C., Banaschewski, T., Barker, G. J., Büchel, C., Desrivières, S., Flor, H., Grigis, A., Garavan, H., Gowland, P. A., et al. (2024) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2024.01.012 · Cited by 5 · see citing works
“Morphological similarity be-tween all cube pairs (ROIs) was calculated based on linear correlation (Tijms et al., 2013), rotating each cube relative to the other one to find the maximum linear correlation between them (this was the final correlation coefficient value considered for each voxel pair).”
BackgroundMethodYang, S., Wu, Y., Sun, L.-F., Lu, Y.-L., Qian, K., Kuang, H., Meng, J., & Wu, Y. (2023) · Brain Science · doi:10.3390/brainsci13101493 · Cited by 4 · see citing works
“The cube-based method constructs an SCN by partitioning the subject’s gray matter into cubes of 6 mm 3 in size [48], defining each cube as a node, and calculating the similarity of each cube Brain Sci. 2023 , 13 , 1493 11 of 13 as an edge, which is a relatively good method for the construction of…”
MethodCai, H.-M., Liu, H., Yang, D., Wu, G.-R., Hu, B., & Chen, J. (2023) · IEEE journal of biomedical and health informatics · doi:10.1109/jbhi.2023.3250711 · Cited by 4 · see citing works
“…an abnormal small-world property; Yao et al. [12] found the greatest clustering coefficient and the longest absolute path length in AD; Tijms et al. [13] found decreased small-world index in AD; Pereira et al. [14] found that all patient groups exhibited increased path length, reduced transitivity,…”
BackgroundOta, M., Numata, Y., Kitabatake, A., Tsukada, E., Kaneta, T., Asada, T., Meno, K., Uchida, K., Suzuki, H., Korenaga, T., et al. (2021) · Psychiatry research. Neuroimaging · doi:10.1016/j.pscychresns.2021.111415 · Cited by 4 · see citing works
Structural similarity networks reveal brain vulnerability in dementia
Montagnese, M., Ebneabbasi, A., García-San-Martín, N., Pecci-Terroba, C., Romero-Garcia, R., Morgan, S., Cole, J., Seidlitz, J., Rittman, T., & Bethlehem, R. (2025) · Alzheimer's & Dementia · doi:10.1002/alz.70973 · Cited by 3 · see citing works
“62,63 The predominance of negative deviations, indicating that regions are becoming less morphometricallysimilartotherestofthecortexthanexpectediscon-sistent with a potential alteration in the coordinated structural organization of the cortex.”
- Authors
- Tijms, B. M., Möller, C., Vrenken, H., Wink, A. M., de Haan, W., van der Flier, W. M., Stam, C. J., Scheltens, P., & Barkhof, F.
- Affiliations
- Amsterdam UMC Location Vrije Universiteit Amsterdam (NL)
- Corresponding author
- Tijms, Betty M.
- ORCID
- Venue
- PLoS ONE
- Publisher
- Public Library of Science (PLoS)
- Published
- 2013-03-11
- Volume
- 8
- Issue
- 3
- Pages
- e58921
- ISSN
- 1932-6203 (ISSN-L)
- PMC
- PMC3594199
- OpenAlex
- W2058087702
- Cited by
- 132
- References
- 102
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 12 · 2023: 8 · 2022: 11 · 2021: 15 · 2020: 11 · 2019: 6 · 2018: 18 · 2017: 11 · 2016: 10 · 2015: 12 · 2014: 7 · 2013: 3
- FWCI
- 5.85
- Type
- journal article
- Language
- en
- Update notices
- correction (2013-09-09)
- Open access
- gold
- doi.org
- Locations
- PLoS ONE (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- UCL Discovery (University College London) (submittedVersion)
- Pure Amsterdam UMC (submittedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Funders
- Stichting Dioraphte
- Alzheimer Nederland
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Keywords
- Alzheimer's disease, structural graph, small-world property, path length, clustering coefficient, cognitive decline, cortical morphology, hippocampus, parahippocampal gyrus, precuneus, fusiform gyrus, gray matter volume, disease prognosis
- MeSH terms
- Aged, Alzheimer Disease, Brain Mapping, Electroencephalography, Female, Humans, Magnetic Resonance Imaging, Male, Psychiatric Status Rating Scales, Severity of Illness Index, Case-Control Studies, Neuroimaging
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