4.6 Article

High-gradient diffusion MRI reveals distinct estimates of axon diameter index within different white matter tracts in the in vivo human brain

期刊

BRAIN STRUCTURE & FUNCTION
卷 225, 期 4, 页码 1277-1291

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00429-019-01961-2

关键词

Axon diameter index; Diffusion; MRI; In vivo; Human brain

资金

  1. NCRR NIH HHS [S10 RR019307, P41EB015896, S10 RR023043, S10 RR023401] Funding Source: Medline
  2. NHLBI NIH HHS [R01 HL131635, R56 HL125590] Funding Source: Medline
  3. NIBIB NIH HHS [R01 EB006847, R01EB006847, R00EB015445, U01 EB026996, P41 EB015896, R00 EB015445] Funding Source: Medline
  4. NIH HHS [U01EB026996, S10RR019307, S10RR023401, S10RR023043] Funding Source: Medline
  5. NIMH NIH HHS [U01MH093765, U01 MH093765] Funding Source: Medline
  6. NINDS NIH HHS [K23 NS078044, R01NS095985, K23NS078044, K23 NS096056, R01 NS095985, K23NS096056] Funding Source: Medline

向作者/读者索取更多资源

Axon diameter and density are important microstructural metrics that offer valuable insight into the structural organization of white matter throughout the human brain. We report the systematic acquisition and analysis of a comprehensive diffusion MRI data set acquired with 300 mT/m maximum gradient strength in a cohort of 20 healthy human subjects that yields distinct and consistent patterns of axon diameter index in white matter tracts of arbitrary orientation. We use a straightforward, previously validated approach to estimating indices of axon diameter and volume fraction that involves interpolating the diffusion signal perpendicular to the principal fiber orientation and fitting a three-compartment model of intra-axonal, extra-axonal and free water diffusion. The resultant maps confirm the presence of larger diameter indices in the body of corpus callosum compared to the genu and splenium, as previously reported, and show larger axon diameter index in the corticospinal tracts compared to adjacent white matter tracts such as the cingulum. An anterior-to-posterior gradient in axon diameter index is also observed, with smaller diameter indices in the frontal lobes and larger diameter indices in the parieto-occipital white matter. These observations are consistent with known trends from prior histologic studies in humans and non-human primates. Rather than serving as fully quantitative measures of axon diameter and density, our results may be considered as axon diameter- and volume fraction-weighted images that appear to be modulated by the underlying microstructure and may capture broad trends in axonal size and packing density, acknowledging that the precise origin of such modulation requires further investigation that will be facilitated by the availability of high gradient strengths for in vivo human imaging.

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