Literature DB >> 30355607

Neurite density is reduced in the presymptomatic phase of C9orf72 disease.

Junhao Wen1,2, Hui Zhang3, Daniel C Alexander3, Stanley Durrleman1,2, Alexandre Routier1,4, Daisy Rinaldi5,6, Marion Houot7, Philippe Couratier8,9, Didier Hannequin10,11, Florence Pasquier12,13, Jiaying Zhang3, Olivier Colliot1,6,14, Isabelle Le Ber15,6,16, Anne Bertrand1,6,17.   

Abstract

OBJECTIVE: To assess the added value of neurite orientation dispersion and density imaging (NODDI) compared with conventional diffusion tensor imaging (DTI) and anatomical MRI to detect changes in presymptomatic carriers of chromosome 9 open reading frame 72 (C9orf72) mutation.
METHODS: The PREV-DEMALS (Predict to Prevent Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis) study is a prospective, multicentre, observational study of first-degree relatives of individuals carrying the C9orf72 mutation. Sixty-seven participants (38 presymptomatic C9orf72 mutation carriers (C9+) and 29 non-carriers (C9-)) were included in the present cross-sectional study. Each participant underwent one single-shell, multishell diffusion MRI and three-dimensional T1-weighted MRI. Volumetric measures, DTI and NODDI metrics were calculated within regions of interest. Differences in white matter integrity, grey matter volume and free water fraction between C9+ and C9- individuals were assessed using linear mixed-effects models.
RESULTS: Compared with C9-, C9+ demonstrated white matter abnormalities in 10 tracts with neurite density index and only 5 tracts with DTI metrics. Effect size was significantly higher for the neurite density index than for DTI metrics in two tracts. No tract had a significantly higher effect size for DTI than for NODDI. For grey matter cortical analysis, free water fraction was increased in 13 regions in C9+, whereas 11 regions displayed volumetric atrophy.
CONCLUSIONS: NODDI provides higher sensitivity and greater tissue specificity compared with conventional DTI for identifying white matter abnormalities in the presymptomatic C9orf72 carriers. Our results encourage the use of neurite density as a biomarker of the preclinical phase. TRIAL REGISTRATION NUMBER: NCT02590276. © Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

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Year:  2018        PMID: 30355607     DOI: 10.1136/jnnp-2018-318994

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  20 in total

Review 1.  The imaging signature of C9orf72 hexanucleotide repeat expansions: implications for clinical trials and therapy development.

Authors:  Stacey Li Hi Shing; Mary Clare McKenna; We Fong Siah; Rangariroyashe H Chipika; Orla Hardiman; Peter Bede
Journal:  Brain Imaging Behav       Date:  2021-01-05       Impact factor: 3.978

Review 2.  Neuroimaging in genetic frontotemporal dementia and amyotrophic lateral sclerosis.

Authors:  Suvi Häkkinen; Stephanie A Chu; Suzee E Lee
Journal:  Neurobiol Dis       Date:  2020-09-02       Impact factor: 5.996

Review 3.  Pre-symptomatic radiological changes in frontotemporal dementia: propagation characteristics, predictive value and implications for clinical trials.

Authors:  Mary Clare McKenna; Jasmin Lope; Ee Ling Tan; Peter Bede
Journal:  Brain Imaging Behav       Date:  2022-08-03       Impact factor: 3.224

Review 4.  Cerebellar pathology in motor neuron disease: neuroplasticity and neurodegeneration.

Authors:  Rangariroyashe H Chipika; Grainne Mulkerrin; Pierre-François Pradat; Aizuri Murad; Fabrice Ango; Cédric Raoul; Peter Bede
Journal:  Neural Regen Res       Date:  2022-11       Impact factor: 6.058

Review 5.  The presymptomatic phase of amyotrophic lateral sclerosis: are we merely scratching the surface?

Authors:  Rangariroyashe H Chipika; We Fong Siah; Mary Clare McKenna; Stacey Li Hi Shing; Orla Hardiman; Peter Bede
Journal:  J Neurol       Date:  2020-10-31       Impact factor: 6.682

6.  Brain structural abnormalities in the preclinical stage of Machado-Joseph disease/spinocerebellar ataxia type 3 (MJD/SCA3): evaluation by MRI morphometry, diffusion tensor imaging and neurite orientation dispersion and density imaging.

Authors:  Mengcheng Li; Xinyuan Chen; Hao-Ling Xu; Ziqiang Huang; Naping Chen; Yuqing Tu; Shirui Gan; Jianping Hu
Journal:  J Neurol       Date:  2021-11-16       Impact factor: 6.682

7.  Early and progressive dysfunction revealed by in vivo neurite imaging in the rNLS8 TDP-43 mouse model of ALS.

Authors:  Akram Zamani; Adam K Walker; Ben Rollo; Katie L Ayers; Raysha Farah; Terence J O'Brien; David K Wright
Journal:  Neuroimage Clin       Date:  2022-04-22       Impact factor: 4.891

8.  Assessing neuraxial microstructural changes in a transgenic mouse model of early stage Amyotrophic Lateral Sclerosis by ultra-high field MRI and diffusion tensor metrics.

Authors:  Rodolfo G Gatto; Carina Weissmann; Manish Amin; Ariel Finkielsztein; Ronen Sumagin; Thomas H Mareci; Osvaldo D Uchitel; Richard L Magin
Journal:  Animal Model Exp Med       Date:  2020-04-16

Review 9.  Emerging Magnetic Resonance Imaging Techniques and Analysis Methods in Amyotrophic Lateral Sclerosis.

Authors:  Andrew W Barritt; Matt C Gabel; Mara Cercignani; P Nigel Leigh
Journal:  Front Neurol       Date:  2018-12-04       Impact factor: 4.003

Review 10.  Diffusion Magnetic Resonance Imaging-Based Biomarkers for Neurodegenerative Diseases.

Authors:  Koji Kamagata; Christina Andica; Ayumi Kato; Yuya Saito; Wataru Uchida; Taku Hatano; Matthew Lukies; Takashi Ogawa; Haruka Takeshige-Amano; Toshiaki Akashi; Akifumi Hagiwara; Shohei Fujita; Shigeki Aoki
Journal:  Int J Mol Sci       Date:  2021-05-14       Impact factor: 5.923

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