Subcomponents and connectivity of the superior longitudinal fasciculus in the human brain
Abstract
The subcomponents of the human superior longitudinal fasciculus (SLF) are disputed. The objective of this study was to investigate the segments, connectivity and asymmetry of the SLF. We performed high angular diffusion spectrum imaging (DSI) analysis on ten healthy adults. We also conducted fiber tracking on a 30-subject DSI template (CMU-30) and 488-subject template from the Human Connectome Project (HCP-488). In addition, five normal brains obtained at autopsy were microdissected. Based on tractography and microdissection results, we show that the human SLF differs significantly from that of monkey. The fibers corresponding to SLF-I found in 6 out of 20 hemispheres proved to be part of the cingulum fiber system in all cases and confirmed on both DSI and HCP-488 template. The most common patterns of connectivity bilaterally were as follows: from angular gyrus to caudal middle frontal gyrus and dorsal precentral gyrus representing SLF-II (or dorsal SLF), and from supramarginal gyrus to ventral precentral gyrus and pars opercularis to form SLF-III (or ventral SLF). Some connectivity features were, however, clearly asymmetric. Thus, we identified a strong asymmetry of the dorsal SLF (SLF-II), where the connectivity between the supramarginal gyrus with the dorsal precentral gyrus and the caudal middle frontal gyrus was only present in the left hemisphere. Contrarily, the ventral SLF (SLF-III) showed fairly constant connectivity with pars triangularis only in the right hemisphere. The results provide a novel neuroanatomy of the SLF that may help to better understand its functional role in the human brain.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
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?
In vivo tractography of the human brain has been evaluated by subjective assessment of plausibility or qualitative visual agreement with post-mortem Klingler-like dissections.
“in vivo tractography of the human brain has been evaluated by subjective assessment of plausibility9, 10 or qualitative visual agreement with post-mortem Klingler-like dissections11, 12.”
From Tractography-based connectomes are dominated by false-positive connections (2016) · cites this paper as [12]
Postmortem macroscopic dissection is unable to identify the distal terminations of bundles.
“but is also unable to identify the distal terminations of bundles (3, 7).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
Martino et al. used dMRI and cortex-sparing fiber dissection and concluded that there were two segments to the SLF, an anterior and a posterior segment.
“Martino et al. used dMRI and cortex-sparing fiber dissection and came to the conclusion that there were two segments to the SLF, an anterior and a posterior segment, much like Martino et al. and Wang et al. (3, 7).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
Wang et al. found a slight asymmetric difference in all SLF sub-components with a tendency toward right-hemispheric dominance.
“Wang et al., on the other hand, found a slight asymmetric difference in all SLF sub-component with a tendency toward right-hemispheric dominance (7).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
Wang et al. consider the SLF as only composed of a dorsal (SLF II) and a ventral (SLF III) segment.
“Hence, they consider the SLF as only composed of a dorsal (SLF II) and a ventral (SLF III) segment.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
In Wang et al.'s construct, the SLF II represents 66% of the total volume, whereas the SLF III about 33%.
“In this construct, the SLF II represents 66% of the total volume, whereas the SLF III about 33%.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
The lateralization of SLF II subcomponents is dominant in the left hemisphere.
“other researchers found the SLF II subcomponents' lateralization to be dominant in the left hemisphere (7, 56, 72).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
Wang et al. concluded that there is a high discrepancy between the simian and human anatomy, so all conclusions derived from the study of the former cannot be applied to the latter.
“The first conclusion is that there is a high discrepancy between the simian and human anatomy; hence, all conclusions derived from the study of the former cannot be applied to the latter.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
The right SLF II preferentially connects the angular gyrus and the superior parietal lobe with the caudal and rostral middle frontal gyrus, respectively.
“the right SLF II preferentially connects the angular gyrus and the superior parietal lobe with the caudal and rostral middle frontal gyrus, respectively.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
The right SLF III has a specific connectivity pattern terminating at the right pars triangularis.
“Wang et al. (7) also reported a specific connectivity pattern for the right SLF III terminating at the right pars triangularis.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
The right SLF III connectivity pattern is probably involved in spatial awareness functioning.
“According to some authors, this connectivity pattern is probably involved in spatial awareness functioning (7).”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
Wang et al. identified a strong bias in leftward connections between the supramarginal gyrus and the dorsal precentral gyrus and the caudal middle frontal gyrus.
“Wang et al. (7) identified a strong bias in leftward connections between the supramarginal gyrus with the dorsal precentral gyrus and the caudal middle frontal gyrus.”
From Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates (2022) · cites this paper as [7]
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
Unbiased average age-appropriate atlases for pediatric studies
Fonov, V., Evans, A. C., Botteron, K., Almli, C. R., McKinstry, R. C., & Collins, D. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.033 · Cited by 2,290 · see citing works
Mapping complex tissue architecture with diffusion spectrum magnetic resonance imaging
Wedeen, V. J., Hagmann, P., Tseng, W. I., Reese, T. G., & Weisskoff, R. M. (2005) · Magnetic Resonance in Medicine · doi:10.1002/mrm.20642 · Cited by 1,339 · see citing works
Makris, N., Kennedy, D. N., McInerney, S., Sorensen, A. G., Wang, R., Caviness, V. S., & Pandya, D. N. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhh186 · Cited by 1,146 · see citing works
A lateralized brain network for visuospatial attention
de Schotten, M. T., Dell'Acqua, F., Forkel, S. J., Simmons, A., Vergani, F., Murphy, D. G. M., & Catani, M. (2011) · Nature Neuroscience · doi:10.1038/nn.2905 · Cited by 1,103 · see citing works
Projections to the frontal cortex from the posterior parietal region in the rhesus monkey
Petrides, M., & Pandya, D. (1984) · The Journal of comparative neurology · doi:10.1002/cne.902280110 · Cited by 1,101 · see citing works
Cortico-cortical connections in the rhesus monkey
Pandya, D. Ν., & Kuypers, H. G. J. M. (1969) · Brain Research · doi:10.1016/0006-8993(69)90141-3 · Cited by 1,085 · see citing works
Generalized ${ q}$-Sampling Imaging
Yeh, F.-C. F., Wedeen, V. J., & Tseng, W. I. (2010) · IEEE Transactions on Medical Imaging · doi:10.1109/tmi.2010.2045126 · Cited by 1,030 · see citing works
Self-citationThiebaut de Schotten, M., ffytche, D. H., Bizzi, A., Dell'Acqua, F., Allin, M., Walshe, M., Murray, R., Williams, S. C., Murphy, D. G. M., & Catani, M. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.07.055 · Cited by 656 · see citing works
Monkey to human comparative anatomy of the frontal lobe association tracts
Thiebaut de Schotten, M., Dell’Acqua, F., Valabregue, R., & Catani, M. (2012) · Cortex · doi:10.1016/j.cortex.2011.10.001 · Cited by 632 · see citing works
NTU-90: A high angular resolution brain atlas constructed by q-space diffeomorphic reconstruction
Yeh, F.-C. F., & Tseng, W. I. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.06.021 · Cited by 509 · see citing works
Self-citationBeyond the arcuate fasciculus: consensus and controversy in the connectional anatomy of language
Dick, A. S., & Tremblay, P. (2012) · Brain · doi:10.1093/brain/aws222 · Cited by 470 · see citing works
Atlas of Human Brain Connections
Catani, M., & Thiebaut de Schotten, M. (2012) · doi:10.1093/med/9780199541164.001.0001 · Cited by 467 · see citing works
The cortical connectivity of the prefrontal cortex in the monkey brain
Yeterian, E. H., Pandya, D. Ν., Tomaiuolo, F., & Petrides, M. (2011) · Cortex · doi:10.1016/j.cortex.2011.03.004 · Cited by 404 · see citing works
Fiber Dissection Technique: Lateral Aspect of the Brain
Türe, U., Yasargil, M. G., Friedman, A. H., & Al‐Mefty, O. (2000) · Neurosurgery · doi:10.1097/00006123-200008000-00028 · Cited by 401 · see citing works
Three-dimensional microsurgical and tractographic anatomy of the white matter of the human brain
Fernández-Miranda, J. C., Rhoton, A. L., Álvarez-Linera, J., Kakizawa, Y., Choi, C., & de Oliveira, E. P. (2008) · Neurosurgery · doi:10.1227/01.neu.0000333767.05328.49 · Cited by 347 · see citing works
Martino, J., De Witt Hamer, P. C., Berger, M. S., Lawton, M. T., Arnold, C. M., de Lucas, E. M., & Duffau, H. (2013) · Brain Structure and Function · doi:10.1007/s00429-012-0386-5 · Cited by 280 · see citing works
High-Definition Fiber Tractography of the Human Brain
Fernandez-Miranda, J. C., Pathak, S., Engh, J. A., Jarbo, K., Verstynen, T., Yeh, F.-C. F., Wang, Y., Mintz, A. H., Boada, F. E., Schneider, W., et al. (2012) · Neurosurgery · doi:10.1227/neu.0b013e3182592faa · Cited by 237 · see citing works
Self-citationAsymmetry, connectivity, and segmentation of the arcuate fascicle in the human brain
Fernandez-Miranda, J., Wang, Y.-B., Pathak, S., Stefaneau, L., Verstynen, T., & Yeh, F.-C. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0751-7 · Cited by 176 · see citing works
Self-citationFernandez-Miranda, J. C., Rhoton, A. L., Kakizawa, Y., Choi, C.-Y., & Álvarez‐Linera, J. (2008) · Journal of neurosurgery · doi:10.3171/jns/2008/108/4/0764 · Cited by 171 · see citing works
Self-citationMaldonado, I. L., Moritz-Gasser, S., & Duffau, H. (2011) · Brain Structure and Function · doi:10.1007/s00429-011-0309-x · Cited by 161 · see citing works
Frontal lobe and posterior parietal contributions to the cortico-cerebellar system
Ramnani, N. (2012) · The Cerebellum · doi:10.1007/s12311-011-0272-3 · Cited by 156 · see citing works
A DTI Investigation of Neural Substrates Supporting Tool Use
Ramayya, A. G., Glasser, M. F., & Rilling, J. K. (2009) · Cerebral Cortex · doi:10.1093/cercor/bhp141 · Cited by 151 · see citing works
The Complex History of the Fronto-Occipital Fasciculus
Schmahmann, J. D., & Pandya, D. Ν. (2007) · Journal of the History of the Neurosciences · doi:10.1080/09647040600620468 · Cited by 147 · see citing works
Rethinking the Role of the Middle Longitudinal Fascicle in Language and Auditory Pathways
Wang, Y., Fernandez-Miranda, J. C., Verstynen, T., Pathak, S., Schneider, W., & Yeh, F.-C. F. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs225 · Cited by 139 · see citing works
Self-citationAgrawal, A., Kapfhammer, J. P., Kress, A., Wichers, H., Deep, A., Feindel, W., Sonntag, V. K. H., Spetzler, R. F., & Preul, M. C. (2011) · Neurosurgery · doi:10.1227/neu.0b013e318214ab79 · Cited by 113 · see citing works
Margulies, D. S., & Petrides, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2259-13.2013 · Cited by 83 · see citing works
Hartwigsen, G., Bestmann, S., Ward, N., Woerbel, S., Mastroeni, C., Granert, O., & Siebner, H. R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1010-12.2012 · Cited by 72 · see citing works
Kawamura, K., & Naito, J. (1984) · Neuroscience Research · doi:10.1016/s0168-0102(84)80007-3 · Cited by 68 · see citing works
The Cerefy Brain Atlases: Continuous Enhancement of the Electronic Talairach–Tournoux Brain Atlas
Nowinski, W. L. (2005) · Neuroinformatics · doi:10.1385/ni:3:4:293 · Cited by 37 · see citing works
Brown, E. C., Jeong, J., Muzik, O., Rothermel, R., Matsuzaki, N., Juhász, C., Sood, S., & Asano, E. (2013) · Human Brain Mapping · doi:10.1002/hbm.22331 · Cited by 36 · see citing works
Jang, S. H., & Hong, J. H. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.10.069 · Cited by 35 · see citing works
White matter in aphasia: A historical review of the Dejerines’ studies
Krestel, H. E., Annoni, J., & Jagella, C. (2013) · Brain and Language · doi:10.1016/j.bandl.2013.05.019 · Cited by 29 · see citing works
Muthusami, P., James, J. S., Thomas, B., Kapilamoorthy, T. R., & Kesavadas, C. (2013) · Journal of Magnetic Resonance Imaging · doi:10.1002/jmri.24528 · Cited by 12 · see citing works
Basser (2000) · doi:10.1002/1522-2594(200010)44:4
Flagged first, then by citations
Cited by
Sorted by citations
Tractography-based connectomes are dominated by false-positive connections
Maier-Hein, K. H., Neher, P., Houde, J.-C., Côté, M.-A., Garyfallidis, E., Zhong, J., Chamberland, M., Yeh, F.-C., Lin, Y.-C., Ji, Q., et al. (2016) · doi:10.1101/084137 · Cited by 1,361 · see citing works
Self-citationChildhood Adversity and Neural Development: A Systematic Review
McLaughlin, K. A., Weissman, D., & Bitrán, D. (2019) · Annual Review of Developmental Psychology · doi:10.1146/annurev-devpsych-121318-084950 · Cited by 892 · see citing works
Sarubbo, S., Tate, M., De Benedictis, A., Merler, S., Moritz-Gasser, S., Herbet, G., & Duffau, H. (2020) · NeuroImage · doi:10.1016/j.neuroimage.2019.116237 · Cited by 206 · see citing works
Superior Longitudinal Fasciculus: A Review of the Anatomical Descriptions With Functional Correlates
Janelle, F., Iorio-Morin, C., D'amour, S., & Fortin, D. (2022) · Frontiers in Neurology · doi:10.3389/fneur.2022.794618 · Cited by 189 · see citing works
Hau, J., Sarubbo, S., Houde, J. C., Corsini, F., Girard, G., Deledalle, C., Crivello, F., Zago, L., Mellet, E., Jobard, G., et al. (2017) · Brain Structure and Function · doi:10.1007/s00429-016-1298-6 · Cited by 121 · see citing works
De Benedictis, A., Petit, L., Descoteaux, M., Marras, C. E., Barbareschi, M., Corsini, F., Dallabona, M., Chioffi, F., & Sarubbo, S. (2016) · Human Brain Mapping · doi:10.1002/hbm.23339 · Cited by 97 · see citing works
Anatomical variability of the arcuate fasciculus: a systematical review
Bernard, F., Zemmoura, I., Ter Minassian, A., Lemée, J.-M., & Menei, P. (2019) · Surgical and Radiologic Anatomy · doi:10.1007/s00276-019-02244-5 · Cited by 55 · see citing works
Neuroanatomical Correlates of the Unity and Diversity Model of Executive Function in Young Adults
Smolker, H. R., Friedman, N. P., Hewitt, J. K., & Banich, M. T. (2018) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2018.00283 · Cited by 42 · see citing works
- Authors
- Wang, X., Pathak, S., Stefaneanu, L., Yeh, F.-C., Li, S., & Fernandez-Miranda, J. C.
- Affiliations
- University of Pittsburgh (US)
- Carnegie Mellon University (US)
- Shanghai Jiao Tong University (CN)
- Corresponding author
- Fernandez-Miranda, Juan C.
- Venue
- Brain Structure and Function
- Published
- 2015-03-18
- Volume
- 221
- Issue
- 4
- Pages
- 2075-2092
- ISSN
- 1863-2653 (ISSN-L)
- 1863-2661
- OpenAlex
- W2049658101
- Cited by
- 257
- References
- 35
- Citations by year
- 2026: 19 · 2025: 23 · 2024: 23 · 2023: 30 · 2022: 33 · 2021: 28 · 2020: 25 · 2019: 25 · 2018: 17 · 2017: 13 · 2016: 16 · 2015: 5
- FWCI
- 13.76
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Brain Structure and Function (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Advanced Neuroimaging Techniques and Applications
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Anatomy › Medical and Biological Sciences
- Keywords
- superior longitudinal fasciculus, cingulum, hemispheric lateralization, white matter connectivity, angular gyrus, supramarginal gyrus, pars opercularis, pars triangularis, diffusion spectrum imaging, tractography
- MeSH terms
- Adult, Brain, Female, Humans, Image Processing, Computer-Assisted, Male, Neural Pathways, Diffusion Magnetic Resonance Imaging, Young Adult, Connectome, White Matter
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