Literature DB >> 30911824

Brain white matter changes in asymptomatic carriers of Leber's hereditary optic neuropathy.

Miaomiao Long1,2, Ling Wang3,4, Qin Tian3,4, Hao Ding1, Wen Qin5, Dapeng Shi6,7, Chunshui Yu8.   

Abstract

OBJECTIVE: Subclinical abnormalities, including microangiopathy, swelling of nerve fibers, visual field abnormalities and visual functional impairments had been reported in Leber's hereditary optic neuropathy (LHON) carriers. The purpose of this study was to investigate microstructural changes of brain white matter in asymptomatic LHON carriers using DTI and tract-based spatial statistics (TBSS).
METHODS: DTI and neuro-ophthalmologic measurements were acquired in 14 LHON carriers and 15 gender- and age-matched healthy controls, and diffusion metrics, including fractional anisotropy (FA), axial (AD), radial diffusion (RD) and mean diffusion (MD) were calculated. Intergroup differences in diffusion metrics were compared regressing out potential nuisance covariates of age and gender. A correlation analysis was performed to test associations between abnormal neuro-ophthalmologic measures and diffusion metrics while controlling the effects of age and gender.
RESULTS: Compared to healthy controls, LHON carriers showed a weak increase of thickness of the retinal nerve fiber layer (RNFL) of the right inferior quadrant (F = 5.22, p = 0.032, before multiple comparison correction). LHON carriers exhibited widespread decreased FA value (bilateral anterior thalamic radiations, bilateral corticospinal tracts, major and minor forceps, bilateral inferior fronto-occipital fasciculi and left superior longitudinal fasciculus), increased RD value (bilateral anterior thalamic radiations, bilateral corticospinal tracts, major and minor forceps, bilateral inferior fronto-occipital fasciculi, bilateral inferior longitudinal fasciculi, bilateral superior longitudinal fasciculi and bilateral uncinate fasciculi) and increased MD value (bilateral anterior thalamic radiations, bilateral corticospinal tracts, minor forceps, bilateral inferior fronto-occipital fasciculi, bilateral inferior longitudinal fasciculi, left superior longitudinal fasciculus and bilateral uncinate fasciculi). Moreover, these changed diffusion metrics were not correlated with age, gender, LHON mutations and retinal measures in LHON carriers.
CONCLUSION: Our results show microstructural alterations in brain white matter in asymptomatic LHON carriers, indicating that LHON-related genetic mutations themselves might result in occult white matter alterations in the brain.

Entities:  

Keywords:  Carriers; Diffusion tensor imaging; Leber’s hereditary optic neuropathy; Retinal nerve fiber layer; Tract-based spatial statistics; White matter

Mesh:

Year:  2019        PMID: 30911824     DOI: 10.1007/s00415-019-09284-2

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  50 in total

1.  Leber's hereditary optic neuropathy (LHON/11778) with myoclonus: report of two cases.

Authors:  V Carelli; M L Valentino; R Liguori; S Meletti; R Vetrugno; F Provini; G L Mancardi; F Bandini; A Baruzzi; P Montagna
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-12       Impact factor: 10.154

2.  Macular nerve fibre and ganglion cell layer changes in acute Leber's hereditary optic neuropathy.

Authors:  Nicole Balducci; Giacomo Savini; Maria Lucia Cascavilla; Chiara La Morgia; Giacinto Triolo; Rosa Giglio; Michele Carbonelli; Vincenzo Parisi; Alfredo A Sadun; Francesco Bandello; Valerio Carelli; Piero Barboni
Journal:  Br J Ophthalmol       Date:  2015-11-27       Impact factor: 4.638

Review 3.  Diffusion tensor imaging of the brain.

Authors:  Andrew L Alexander; Jee Eun Lee; Mariana Lazar; Aaron S Field
Journal:  Neurotherapeutics       Date:  2007-07       Impact factor: 7.620

4.  Evidence for retrochiasmatic tissue loss in Leber's hereditary optic neuropathy.

Authors:  Valeria Barcella; Maria A Rocca; Stefania Bianchi-Marzoli; Jacopo Milesi; Lisa Melzi; Andrea Falini; Luisa Pierro; Massimo Filippi
Journal:  Hum Brain Mapp       Date:  2010-05-13       Impact factor: 5.038

5.  Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia.

Authors:  D D De Vries; L N Went; G W Bruyn; H R Scholte; R M Hofstra; P A Bolhuis; B A van Oost
Journal:  Am J Hum Genet       Date:  1996-04       Impact factor: 11.025

6.  Long term cortical plasticity in visual retinotopic areas in humans with silent retinal ganglion cell loss.

Authors:  Otília C d'Almeida; Catarina Mateus; Aldina Reis; Manuela M Grazina; Miguel Castelo-Branco
Journal:  Neuroimage       Date:  2013-05-16       Impact factor: 6.556

7.  Association of the 11778 mitochondrial DNA mutation and demyelinating disease.

Authors:  K M Flanigan; D R Johns
Journal:  Neurology       Date:  1993-12       Impact factor: 9.910

8.  Natural history of Leber's hereditary optic neuropathy: longitudinal analysis of the retinal nerve fiber layer by optical coherence tomography.

Authors:  Piero Barboni; Michele Carbonelli; Giacomo Savini; Carolina do V F Ramos; Arturo Carta; Adriana Berezovsky; Solange R Salomao; Valerio Carelli; Alfredo A Sadun
Journal:  Ophthalmology       Date:  2010-01-19       Impact factor: 12.079

9.  Leber's hereditary optic neuropathy, intellectual disability and epilepsy presenting with variable penetrance associated to the m.3460G >A mutation and a heteroplasmic expansion of the microsatellite in MTRNR1 gene - case report.

Authors:  Angelica Bianco; Luigi Bisceglia; Maria Fara De Caro; Valeria Galeandro; Patrizia De Bonis; Apollonia Tullo; Stefano Zoccolella; Silvana Guerriero; Vittoria Petruzzella
Journal:  BMC Med Genet       Date:  2018-07-27       Impact factor: 2.103

10.  Mitochondrial DNA copy number in affected and unaffected LHON mutation carriers.

Authors:  Angelica Bianco; Alessio Valletti; Giovanna Longo; Luigi Bisceglia; Julio Montoya; Sonia Emperador; Silvana Guerriero; Vittoria Petruzzella
Journal:  BMC Res Notes       Date:  2018-12-20
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  2 in total

1.  Leber's hereditary optic neuropathy with diffuse white matter changes mimicking gliomatosis cerebri: illustrative case.

Authors:  Wakiko Saruta; Ichiyo Shibahara; Hajime Handa; Madoka Inukai; Shunsuke Kanayama; Ryoma Yasumoto; Keizo Sakurai; Hisanao Akiyama; Hitoshi Ishikawa; Sumito Sato; Takuichiro Hide; Toshihiro Kumabe
Journal:  J Neurosurg Case Lessons       Date:  2021-06-28

2.  Characterization of Brain Microstructural Abnormalities in High Myopia Patients: A Preliminary Diffusion Kurtosis Imaging Study.

Authors:  Huihui Wang; Hongwei Wen; Jing Li; Qian Chen; Shanshan Li; Yanling Wang; Zhenchang Wang
Journal:  Korean J Radiol       Date:  2021-05-04       Impact factor: 3.500

  2 in total

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