Eight healthy volunteers were scanned at 7T using a line-scan diffusion sequence with each line prescribed perpendicularly to primary somatosensory (S1) and motor (M1) cortex, and with 250–500 micron resolution along the line. We observed tangential diffusion in S1 and radial diffusion in M1, consistent with prior reports, but with the high radial resolution used here enabling us to identify the deep layers of S1—where high diffusion anisotropy was seen—as the source of the tangential diffusion, with low anisotropy in the upper layers. In M1, radial diffusion with moderate anisotropy was seen at nearly all cortical depths.
Eight healthy volunteers (6F/2M, ages: 22–30 years), having given informed consent, were scanned on a Siemens 7T whole-body scanner using a custom-built 31-channel head receive coil and birdcage transmit coil. On each volunteer, a 0.75×0.75×0.75 mm3 FOCI-ME-MPRAGE scan[9] was acquired and used as the anatomical localizer for subsequent line-scan diffusion acquisitions[7,8], with each line prescribed as perpendicularly as possible to primary somatosensory cortex S1 and primary motor cortex M1 (Fig. 1). The parameters common to all line-scan acquisitions were as follows: TR/TE = 2000/50 ms, BW ≈ 100 Hz/pixel and 19 b-values equally spaced from 100 to 1000 s/mm2. The voxel size along the line was either 250 or 500 μm, with a 256 mm readout field-of-view and nominal line thickness of 3 mm. Three variants of the line-scan acquisitions were employed: (i) “3dir-250μm” (volunteers 1–7), with three diffusion directions, one in the radial direction (i.e., parallel to the line) and two tangential directions perpendicular to the line and to each other, at 250-μm radial resolution (four repetitions, TA = ~8 minutes), (ii) “13dir-500μm” (volunteers 4–6), with an additional ten diffusion directions approximately uniformly distributed on the unit hemisphere, at 500-μm radial resolution (one repetition, TA = ~9 minutes) and (iii) “13dir-250μm” (volunteers 3, 6 and 8), with the thirteen directions as above, but at 250-μm radial resolution (three repetitions, TA = ~27 minutes).
For signal reconstruction, phase-corrected complex-valued signals were averaged across repetitions prior to root-sum-of-squares coil combination[5]. For the 3dir-250μm data, the monoexponential model was then fitted per-voxel and per-direction to the resulting signal versus b-value, yielding an apparent diffusion coefficient for each direction. For the 13dir-500μm and 13dir-250μm data, per-voxel fits to the (single) tensor model were performed. Fractional anisotropy[10] (FA) and “radiality” measures were then derived, where radiality is defined as the cosine of the angle between the diffusion tensor primary eigenvector and the cortical surface normal, defined only for voxels with FA≥0.05[11,12].
Fig. 2 shows 3dir-250μm results from volunteer 1. In the deeper layers of S1, diffusion coefficients in the radial direction (red) appear to be substantially lower than in the tangential directions (green and blue). In upper S1, the diffusion coefficients for the three directions appear to be very similar, suggesting little diffusion anisotropy there. This pattern in S1 can be seen consistently across volunteers (Fig. 3). In M1, higher diffusion coefficients in the radial versus the tangential directions can readily be seen in many, but not all, volunteers.
Fig. 4 shows 13dir-500μm and 13dir-250μm results from volunteer 6 and Fig. 5 shows corresponding results from volunteers 3, 4, 5 and 8. In deep S1, high FA and low radiality values are seen, indicating predominantly tangential diffusion, whereas low FA values are seen in upper S1. In M1, moderate FA and high radiality values are seen at most cortical depths. Although the pattern described above can be appreciated at both in-line resolutions, the 13dir-250μm data allow observation of a greater number of samples within cortex—especially important for S1, which is one of the thinnest cortical areas.
[1] Hubel DH. Eye, Brain, and Vision. Scientific American Library 1988.
[2] Vogt C, Vogt O. Allgemeinere ergebnisse unserer hirnforschung. J Physiol Neurol (Leipz.) 1919;25:279–462.
[3] Yu X, Qian C, Chen DY, Dodd SJ, Koretsky AP. Deciphering laminar-specific neural inputs with line-scanning fMRI. Nat Methods 2014;11:55–58.
[4] Kashyap S, Ivanov D, Sengupta S, Poser BA, Uludağ K. True laminar resolution fMRI of the human visual cortex at 7T. Proc Intl Soc Mag Reson Med 2018;26:394.
[5] Balasubramanian M, Mulkern RV, Neil JJ, Maier SE, Polimeni JR. In-vivo line-scan diffusion MR at 250 micron inline resolution within human cerebral cortex at 7T. Proc Intl Soc Mag Reson Med 2018;26:1618.
[6] Mansfield P, Maudsley AA. Line scan proton spin imaging in biological structures by NMR. Phys Med Biol 1976;21:847–852.
[7] Chenevert TL, Pipe JG, Williams DM, Brunberg JA. Quantitative measurement of tissue perfusion and diffusion in vivo. Magn Reson Med 1991;17:197–212.
[8] Gudbjartsson H, Maier SE, Mulkern RV, Mórocz IA, Patz S, Jolesz FA. Line scan diffusion imaging. Magn Reson Med 1996;36:509–519.
[9] Zaretskaya N, Fischl B, Reuter M, Renvall V, Polimeni JR. Advantages of cortical surface reconstruction using submillimeter 7 T MEMPRAGE. Neuroimage 2018; 165:11-26.
[10] Basser PJ, Pierpaoli C. Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI. J Magn Reson B 1996;111:209–219.
[11] Anwander A, Pampel A, Knösche TR. In vivo measurement of cortical anisotropy by diffusion-weighted imaging correlates with cortex type. Proc Intl Soc Mag Reson Med 2010;18:109.
[12] McNab JA, Polimeni JR, Wang R, Augustinack JC, Fujimoto K, Stevens A, Triantafyllou C, Janssens T, Farivar R, Folkerth RD, Vanduffel W, Wald LL. Surface based analysis of diffusion orientation for identifying architectonic domains in the in vivo human cortex. Neuroimage 2013;69:87–100.