Vol 76, No 4 (2017)
Original article
Published online: 2017-04-26

open access

Page views 2639
Article views/downloads 2477
Get Citation

Connect on Social Media

Connect on Social Media

Frontal aslant tract projections to the inferior frontal gyrus

T. Szmuda, M. Rogowska, P. Słoniewski, A. Abuhaimed, M. Szmuda, J. Springer, A. Sabisz, J. Dzierżanowski, A. Starzyńska, T. Przewoźny
Pubmed: 28553860
Folia Morphol 2017;76(4):574-581.

Abstract

Background: Frontal aslant tract (FAT) is a white matter bundle connecting the pre-supplementary motor area (pre-SMA) and the supplementary motor area (SMA) with the inferior frontal gyrus (IFG). The purpose of the present study was to evaluate the anatomical variability of FAT.

Materials and methods: Total number of fibres and the lateralisation index (LI) were calculated. We attempted to find factors contributing to the diversity of FAT regarding IFG terminations to the pars opercularis (IFG-Op) and to the pars triangularis (IFG-Tr). Magnetic resonance imaging of adult patients with diffusion tensor imaging (DTI) with total number of 98 hemispheres composed a cohort. V-shaped operculum was the most common (60.5%).

Results: Total number of FAT fibres had widespread and unimodal distribution (6 to 1765; median: 160). Left lateralisation was noted in 64.3% of cases and was positively correlated with total number of FAT fibres and the bundle projecting to IFG-Op (p < 0.01). LI correlated with total number of FAT fibres (r = 0.43, p < 0.01). FAT projected predominantly to IFG-Op (88.9%; 88 of 99). Only in 3 (3.1%) cases more fibres terminated in IFG-Tr than in IFG-Op. Total number of FAT fibres and number of fibres terminating at IFG-Op did not correlate with the ratio of fibre numbers: FAT/IFG-Op, FAT/IFG-Tr and IFG-Op/IFG-Tr (p > 0.05). The greater total number of fibres to IFG-Tr was, the higher were the ratios of IFG-Tr/ /FAT (r = 0.57, p < 0.01) and IFG-Tr/IFG-Op (r = 0.32, p = 0.04).

Conclusions: Among the IFG, the major termination of FAT is IFG-Op. Whereas the IFG-Tr projection seems to be related to the expansion of the entire FAT bundle regardless of side, domination and handedness. Nevertheless, FAT features a significant anatomical variability which cannot be explained in terms of DTI findings.

Article available in PDF format

View PDF Download PDF file

References

  1. Alario FX, Chainay H, Lehericy S, et al. The role of the supplementary motor area (SMA) in word production. Brain Res. 2006; 1076(1): 129–143.
  2. Ayberk G, Yagli OE, Comert A, et al. Anatomic relationship between the anterior sylvian point and the pars triangularis. Clin Anat. 2012; 25(4): 429–436.
  3. Broce I, Bernal B, Altman N, et al. Fiber tracking of the frontal aslant tract and subcomponents of the arcuate fasciculus in 5-8-year-olds: Relation to speech and language function. Brain Lang. 2015; 149: 66–76.
  4. Catani M, Dell'acqua F, Vergani F, et al. Short frontal lobe connections of the human brain. Cortex. 2012; 48(2): 273–291.
  5. Catani M, Mesulam MM, Jakobsen E, et al. A novel frontal pathway underlies verbal fluency in primary progressive aphasia. Brain. 2013; 136(Pt 8): 2619–2628.
  6. Dhakar MB, Ilyas M, Jeong JW, et al. Frontal aslant tract abnormality on diffusion tensor imaging in an aphasic patient with 49, XXXXY syndrome. Pediatr Neurol. 2016; 55: 64–67.
  7. Foundas AL, Weisberg A, Browning CA, et al. Morphology of the frontal operculum: a volumetric magnetic resonance imaging study of the pars triangularis. J Neuroimaging. 2001; 11(2): 153–159.
  8. Fujii M, Maesawa S, Ishiai S, et al. Neural Basis of Language: An Overview of An Evolving Model. Neurol Med Chir (Tokyo). 2016; 56(7): 379–386.
  9. Fujii M, Maesawa S, Motomura K, et al. Intraoperative subcortical mapping of a language-associated deep frontal tract connecting the superior frontal gyrus to Broca's area in the dominant hemisphere of patients with glioma. J Neurosurg. 2015; 122(6): 1390–1396.
  10. Kemerdere R, de Champfleur NM, Deverdun J, et al. Role of the left frontal aslant tract in stuttering: a brain stimulation and tractographic study. J Neurol. 2016; 263(1): 157–167.
  11. Kinoshita M, de Champfleur NM, Deverdun J, et al. Role of fronto-striatal tract and frontal aslant tract in movement and speech: an axonal mapping study. Brain Struct Funct. 2015; 220(6): 3399–3412.
  12. Kronfeld-Duenias V, Amir O, Ezrati-Vinacour R, et al. The frontal aslant tract underlies speech fluency in persistent developmental stuttering. Brain Struct Funct. 2016; 221(1): 365–381.
  13. Martino J, de Lucas EM, Ibáñez-Plágaro FJ, et al. Foix-Chavany-Marie syndrome caused by a disconnection between the right pars opercularis of the inferior frontal gyrus and the supplementary motor area. J Neurosurg. 2012; 117(5): 844–850.
  14. Qiu D, Tan LH, Siok WT, et al. Lateralization of the arcuate fasciculus and its differential correlation with reading ability between young learners and experienced readers: a diffusion tensor tractography study in a Chinese cohort. Hum Brain Mapp. 2011; 32(12): 2054–2063.
  15. Rizio AA, Diaz MT. Language, aging, and cognition: frontal aslant tract and superior longitudinal fasciculus contribute toward working memory performance in older adults. Neuroreport. 2016; 27(9): 689–693.
  16. Sierpowska J, Gabarrós A, Fernandez-Coello A, et al. Morphological derivation overflow as a result of disruption of the left frontal aslant white matter tract. Brain Lang. 2015; 142: 54–64.
  17. Tanaka N, Grant PE, Suzuki N, et al. Multimodal imaging of spike propagation: a technical case report. AJNR Am J Neuroradiol. 2012; 33(6): E82–E84.
  18. Tremblay P, Dick AS. Broca and Wernicke are dead, or moving past the classic model of language neurobiology. Brain Lang. 2016; 162: 60–71.
  19. Vassal F, Boutet C, Lemaire JJ, et al. New insights into the functional significance of the frontal aslant tract: an anatomo-functional study using intraoperative electrical stimulations combined with diffusion tensor imaging-based fiber tracking. Br J Neurosurg. 2014; 28(5): 685–687.
  20. Vergani F, Lacerda L, Martino J, et al. White matter connections of the supplementary motor area in humans. J Neurol Neurosurg Psychiatry. 2014; 85(12): 1377–1385.