Volumetric Differences in Gray and White Matter of Cerebellar Crus I/ II across the Different Clinical Stages of Schizophrenia

AbstractThe contribution of cerebellar pathology to cognitive and behavioural manifestations is increasingly recognised, but the cerebellar profiles of FTD phenotypes are relatively poorly characterised. A prospective, single-centre imaging study has been undertaken with a high-resolution structural and diffusion tensor protocol to systematically evaluate cerebellar grey and white matter alterations in behavioural-variant FTD(bvFTD), non-fluent variant primary progressive aphasia(nfvPPA), semantic-variant primary progressive aphasia(svPPA), C9orf72-positive ALS-FTD(C9 + ALSFTD) and C9orf72-negative ALS-FTD(C9-ALSFTD). Cerebellar cortical thickness and complementary morphometric analyses were carried out to appraise atrophy patterns controlling for demographic variables. White matter integrity was assessed in a study-specific white matter skeleton, evaluating three diffusivity metrics: fractional anisotropy (FA), axial diffusivity (AD) and radial diffusivity (RD). Significant cortical thickness reductions were identified in: lobule VII and crus I in bvFTD; lobule VI VII, crus I and II in nfvPPA; and lobule VII, crus I and II in svPPA; lobule IV, VI, VII and Crus I and II in C9 + ALSFTD. Morphometry revealed volume reductions in lobule V in all groups; in addition to lobule VIII in C9 + ALSFTD; lobule VI, VIII and vermis in C9-ALSFTD; lobule V, VII and vermis in bvFTD; and lobule V, VI, VIII and vermis in nfvPPA. Widespread white matter alterations were demonstrated by significant fractional anisotropy, axial diffusivity and radial diffusivity changes in each FTD phenotype that were more focal in those with C9 + ALSFTD and svPPA. Our findings indicate that FTD subtypes are associated with phenotype-specific cerebellar signatures with the selective involvement of specific lobules instead of global cerebellar atrophy.

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White matter microstructural and morphometric alterations in autism: Implications for intellectual and verbal capabilities

10.1101/2021.10.11.464005 ◽

2021 ◽

Author(s):

Chun-Hung Yeh ◽

Rung-Yu Tseng ◽

Hsing-Chang Ni ◽

Luca Cocchi ◽

Jung-Chi Chang ◽

...

Keyword(s):

White Matter ◽

Corpus Callosum ◽

Dorsolateral Prefrontal Cortex ◽

Autism Spectrum ◽

Typically Developing ◽

Diffusion Weighted Mri ◽

Fiber Density ◽

Dorsolateral Prefrontal ◽

Crus I ◽

The Right

ABSTRACTBackgroundNeuroimage literature of autism spectrum disorder (ASD) has a moderate-to-high risk of bias, partially because those combined with intellectual impairment (II) and/or minimally verbal (MV) status are generally ignored. We aimed to provide more comprehensive insights into white matter alterations of ASD, inclusive of individuals with II (ASD-II-Only) or MV expression (ASD-MV).MethodsSixty-five participants with ASD (ASD-Whole; 16.6±5.9 years; comprising 34 intellectually able youth, ASD-IA, and 31 intellectually impaired youth, ASD-II, including 24 ASD-II-Only plus 7 ASD-MV) and 38 demographic-matched typically developing controls (TDC; 17.3±5.6 years) were scanned in accelerated diffusion-weighted MRI. Fixel-based analysis was undertaken to investigate the categorical differences in fiber density (FD), fiber cross-section (FC), and a combined index (FDC), and brain-symptom/cognition associations.ResultsASD-Whole had reduced FD in the anterior and posterior corpus callosum and left cerebellum Crus I, and smaller FDC in right cerebellum Crus II, compared to TDC. ASD-II, relative to TDC, showed almost identical alterations to those from ASD-Whole vs. TDC. ASD-II-Only had greater FD/FDC in the isthmus-splenium of callosum than ASD-MV. Autistic severity negatively correlated with FC in right Crus I. Non-verbal full-scale IQ positively correlated with FC/FDC in cerebellum VI. FD/FDC of the right dorsolateral prefrontal cortex showed a diagnosis-by-executive function interaction.ConclusionsASD-associated white matter alterations appear driven by individuals combined with II and/or MV. Results suggest that changes in the corpus callosum and cerebellum are key for psychopathology and cognition associated with ASD. Our work highlights an essential to include understudied sub-populations on the spectrum in research.

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Grey and white matter atrophy in early clinical stages of primary progressive multiple sclerosis

NeuroImage ◽

10.1016/j.neuroimage.2004.02.008 ◽

2004 ◽

Vol 22 (1) ◽

pp. 353-359 ◽

Cited By ~ 58

Author(s):

Jaume Sastre-Garriga ◽

Gordon T Ingle ◽

Declan T Chard ◽

Lluı́s Ramió-Torrentà ◽

David H Miller ◽

...

Keyword(s):

Multiple Sclerosis ◽

White Matter ◽

Progressive Multiple Sclerosis ◽

Primary Progressive Multiple Sclerosis ◽

Primary Progressive ◽

Clinical Stages

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Review for "The distribution, number and certain neurochemical identities of infracortical white matter neurons in the brains of three megachiropteran bat species"

10.1002/cne.24894/v1/review2 ◽

2020 ◽

Keyword(s):

White Matter

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FT-IR microspectroscopic analysis of diseased white matter brain tissues

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100141214 ◽

1995 ◽

Vol 53 ◽

pp. 968-969

Author(s):

Steven M. Le Vine ◽

David L. Wetzel

Keyword(s):

White Matter ◽

Gray Matter ◽

Twitcher Mouse ◽

Grid Pattern ◽

Marked Contrast ◽

Spatially Resolved ◽

Ft Ir ◽

Ir Microspectroscopy ◽

Chemical Evidence

In situ FT-IR microspectroscopy has allowed spatially resolved interrogation of different parts of brain tissue. In previous work the spectrrscopic features of normal barin tissue were characterized. The white matter, gray matter and basal ganglia were mapped from appropriate peak area measurements from spectra obtained in a grid pattern. Bands prevalent in white matter were mostly associated with the lipid. These included 2927 and 1469 cm-1 due to CH2 as well as carbonyl at 1740 cm-1. Also 1235 and 1085 cm-1 due to phospholipid and galactocerebroside, respectively (Figs 1and2). Localized chemical changes in the white matter as a result of white matter diseases have been studied. This involved the documentation of localized chemical evidence of demyelination in shiverer mice in which the spectra of white matter lacked the marked contrast between it and gray matter exhibited in the white matter of normal mice (Fig. 3).The twitcher mouse, a model of Krabbe’s desease, was also studied. The purpose in this case was to look for a localized build-up of psychosine in the white matter caused by deficiencies in the enzyme responsible for its breakdown under normal conditions.

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