Brain Abnormalities in Congenital Fibrosis of the Extraocular Muscles Type 1: A Multimodal MRI Imaging Study

PLoS One. 2015 Jul 17;10(7):e0133473. doi: 10.1371/journal.pone.0133473. eCollection 2015.

Abstract

Purpose: To explore the possible brain structural and functional alterations in congenital fibrosis of extraocular muscles type 1 (CFEOM1) patients using multimodal MRI imaging.

Methods: T1-weighted, diffusion tensor images and functional MRI data were obtained from 9 KIF21A positive patients and 19 age- and gender-matched healthy controls. Voxel based morphometry and tract based spatial statistics were applied to the T1-weighted and diffusion tensor images, respectively. Amplitude of low frequency fluctuations and regional homogeneity were used to process the functional MRI data. We then compared these multimodal characteristics between CFEOM1 patients and healthy controls.

Results: Compared with healthy controls, CFEOM1 patients demonstrated increased grey matter volume in bilateral frontal orbital cortex and in the right temporal pole. No diffusion indices changes were detected, indicating unaffected white matter microstructure. In addition, from resting state functional MRI data, trend of amplitude of low-frequency fluctuations increases were noted in the right inferior parietal lobe and in the right frontal cortex, and a trend of ReHo increase (p<0.001 uncorrected) in the left precentral gyrus, left orbital frontal cortex, temporal pole and cingulate gyrus.

Conclusions: CFEOM1 patients had structural and functional changes in grey matter, but the white matter was unaffected. These alterations in the brain may be due to the abnormality of extraocular muscles and their innervating nerves. Future studies should consider the possible correlations between brain morphological/functional findings and clinical data, especially pertaining to eye movements, to obtain more precise answers about the role of brain area changes and their functional consequence in CFEOM1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Brain / abnormalities*
  • Brain / pathology
  • Brain Mapping
  • Eye Diseases, Hereditary / diagnosis
  • Female
  • Fibrosis
  • Gray Matter / abnormalities
  • Gray Matter / pathology
  • Humans
  • Magnetic Resonance Imaging / methods*
  • Male
  • Multimodal Imaging*
  • Ophthalmoplegia

Supplementary concepts

  • Congenital Fibrosis of the Extraocular Muscles

Grants and funding

This work was partly supported by the National Natural Science Foundation of China (81070762, 61271151, 81401397 and 61201066), 863 Project (2013AA013803) and Beijing Natural Science Foundation (7152039). Prof. Sabel was partly supported by Chinese Academy of Sciences Senior Visiting Professorships Programs and by the "Hai-ju" by Beijing Overseas Talents Program at Beijing Tongren Hospital. The funding organizations had no role in design or conduct of this research.