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Characterizing Intraorbital Optic Nerve Changes on Diffusion Tensor Imaging in Thyroid Eye Disease Before Dysthyroid
Journal of Computer Assisted Tomography
|September 23, 2017
Summary
Thyroid eye disease (TED) alters optic nerve diffusion tensor imaging (DTI) parameters, indicating nerve changes before dysthyroid optic neuropathy. Fractional anisotropy (FA) specifically reflects TED activity and severity.
Area of Science:
- Ophthalmology
- Neurology
- Radiology
Background:
- Thyroid eye disease (TED) is an autoimmune condition affecting the orbit.
- Dysthyroid optic neuropathy (DON) is a severe complication of TED, potentially leading to vision loss.
- Early detection of optic nerve involvement in TED is crucial for timely intervention.
Purpose of the Study:
- To investigate optic nerve changes in TED patients before DON development using diffusion tensor imaging (DTI).
- To assess if DTI parameters can detect subclinical optic nerve alterations in TED.
- To correlate DTI findings with clinical activity and severity of TED.
Main Methods:
- Diffusion tensor imaging (DTI) was used to measure mean, axial, and radial diffusivity, and fractional anisotropy (FA) in the optic nerves of 20 TED patients and 20 controls.
- Extraocular muscle diameters were measured using computed tomography.
- DTI parameters were compared between TED patients and controls, and between active and inactive TED stages. Correlations with clinical features were analyzed.
Main Results:
- TED patients showed lower mean, axial, and radial diffusivities, and higher FA compared to controls.
- Radial diffusivity was lower in active TED versus inactive TED.
- FA positively correlated with clinical activity, modified NOSPECS score, and extraocular muscle thickness. Radial and axial diffusivity correlated with modified NOSPECS score and exophthalmos degree, respectively.
Conclusions:
- DTI parameters, including FA and diffusivities, reveal optic nerve alterations in TED patients prior to the onset of DON.
- FA is a sensitive indicator of TED activity and disease severity, reflecting subclinical optic nerve changes.

