4.7 Article

Retinal ganglion cell endowment is correlated with optic tract fiber cross section, not density

期刊

NEUROIMAGE
卷 260, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2022.119495

关键词

Fixel-based analysis; Retinal ganglion cell endowment; Visual pathway variations

资金

  1. NIH [R01EY028601, R01EY030227, P30EY001583, U01EY025864, P30 EY001583, R01EB022744, P41EB015922]
  2. Low Vision Research Award from the Research to Prevent Blindness/Lions Clubs International Foundation
  3. Foundation Fighting Blindness
  4. NSF [DGE-1845298]

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There is considerable variation in the number of retinal ganglion cells (RGC) in the eye, which leads to variations in the optic tracts and subsequent structures along the visual pathway. Using diffusion MR analysis, the study investigated the correlation between RGC tissue volume and fiber density (FD) and cross section (FC) measurements from the optic tracts. The results showed that RGC endowment is correlated with FC but not with FD. Additionally, variations in each visual area were found to be correlated with variations in immediately adjacent visual structures.
There is substantial variation between healthy individuals in the number of retinal ganglion cells (RGC) in the eye, with commensurate variation in the number of axons in the optic tracts. Fixel-based analysis of diffusion MR produces estimates of fiber density (FD) and cross section (FC). Using these fixel measurements along with retinal imaging, we asked if individual differences in RGC tissue volume are correlated with individual differences in FD and FC measurements obtained from the optic tracts, and subsequent structures along the cortical visual pathway. We find that RGC endowment is correlated with optic tract FC, but not with FD. RGC volume had a decreasing relationship with measurements from subsequent regions of the visual system (LGN volume, optic radiation FC/FD, and V1 surface area). However, we also found that the variations in each visual area were correlated with the variations in its immediately adjacent visual structure. We only observed these serial correlations when FC is used as the measure of interest for the optic tract and radiations, but no significant relationship was found when FD represented these white matter structures. From these results, we conclude that the variations in RGC endowment, LGN volume, and V1 surface area are better predicted by the overall cross section of the optic tract and optic radiations as compared to the intra-axonal restricted signal component of these white matter pathways. Additionally, the presence of significant correlations between adjacent, but not distant, anatomical structures suggests that there are multiple, local sources of anatomical variation along the visual pathway.

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