TY - JOUR
T1 - Whole-brain voxel-based analysis of diffusion tensor MRI parameters in patients with primary open angle glaucoma and correlation with clinical glaucoma stage
AU - Dai, Hui
AU - Yin, Dazhi
AU - Hu, Chunhong
AU - Morelli, John N.
AU - Hu, Su
AU - Yan, Xu
AU - Xu, Dongrong
PY - 2013/2
Y1 - 2013/2
N2 - Introduction: Glaucoma is the second leading cause of blindness worldwide. The purpose of this study is to identify areas of neurodegeneration in glaucoma utilizing 3 T magnetic resonance (MR) diffusion tensor imaging (DTI) parameters with whole-brain voxel-based analysis (VBA) and determine whether these parameters correlate with disease severity. Methods: Twenty-five glaucoma patients and 25 age-matched healthy volunteers were prospectively examined. Clinical glaucoma severity was assessed utilizing static threshold visual field parameters. All subjects underwent 3 T MRI utilizing a DTI sequence (repetition time/echo time 13,000/68.9 ms, maximal b value 800 s/mm2 along 30 directions) and an anatomic sequence to provide structural information. All data sets were processed by VBA. Brain fractional anisotropy, mean diffusivity (MD), radial diffusivity (RD), and axial diffusivity (AD) were compared in the two groups. Correlation between DTI parameters and glaucoma stage were determined. Results: The bilateral optic radiations and chiasma of glaucoma patients demonstrated statistically significantly lower fractional anisotropy (p < 0.05). Optic radiation RD was similarly decreased in glaucoma patients (p < 0.05). There were no statistically significant differences noted in MD or AD between the two groups (p > 0.05). Optic chiasm fractional anisotropy values were negatively correlated with glaucoma stage (r = -0.53, p < 0.05) and optic radiation RD values positively correlated (left r = 0.45, p < 0.05; right = 0.38, p = 0.06). Conclusion: DTI parameters fractional anisotropy and RD are altered in the optic chiasm and radiations of glaucoma patients. As fractional anisotropy and RD also correlate with glaucoma stage, these values could serve as potential noninvasive markers of disease severity.
AB - Introduction: Glaucoma is the second leading cause of blindness worldwide. The purpose of this study is to identify areas of neurodegeneration in glaucoma utilizing 3 T magnetic resonance (MR) diffusion tensor imaging (DTI) parameters with whole-brain voxel-based analysis (VBA) and determine whether these parameters correlate with disease severity. Methods: Twenty-five glaucoma patients and 25 age-matched healthy volunteers were prospectively examined. Clinical glaucoma severity was assessed utilizing static threshold visual field parameters. All subjects underwent 3 T MRI utilizing a DTI sequence (repetition time/echo time 13,000/68.9 ms, maximal b value 800 s/mm2 along 30 directions) and an anatomic sequence to provide structural information. All data sets were processed by VBA. Brain fractional anisotropy, mean diffusivity (MD), radial diffusivity (RD), and axial diffusivity (AD) were compared in the two groups. Correlation between DTI parameters and glaucoma stage were determined. Results: The bilateral optic radiations and chiasma of glaucoma patients demonstrated statistically significantly lower fractional anisotropy (p < 0.05). Optic radiation RD was similarly decreased in glaucoma patients (p < 0.05). There were no statistically significant differences noted in MD or AD between the two groups (p > 0.05). Optic chiasm fractional anisotropy values were negatively correlated with glaucoma stage (r = -0.53, p < 0.05) and optic radiation RD values positively correlated (left r = 0.45, p < 0.05; right = 0.38, p = 0.06). Conclusion: DTI parameters fractional anisotropy and RD are altered in the optic chiasm and radiations of glaucoma patients. As fractional anisotropy and RD also correlate with glaucoma stage, these values could serve as potential noninvasive markers of disease severity.
KW - Diffusion tensor imaging
KW - Magnetic resonance imaging
KW - Primary open-angle glaucoma
KW - Voxel-based analysis
UR - https://www.scopus.com/pages/publications/84873705893
U2 - 10.1007/s00234-012-1122-9
DO - 10.1007/s00234-012-1122-9
M3 - 文章
C2 - 23223846
AN - SCOPUS:84873705893
SN - 0028-3940
VL - 55
SP - 233
EP - 243
JO - Neuroradiology
JF - Neuroradiology
IS - 2
ER -