首页> 外文期刊>Investigative ophthalmology & visual science >Retrobulbar optic nerve diameter measured by high-speed magnetic resonance imaging as a biomarker for axonal loss in glaucomatous optic atrophy.
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Retrobulbar optic nerve diameter measured by high-speed magnetic resonance imaging as a biomarker for axonal loss in glaucomatous optic atrophy.

机译:眼球后视神经直径通过高速磁共振成像测量,作为青光眼性视神经萎缩中轴突丢失的生物标记。

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PURPOSE: To assess a novel magnetic resonance imaging (MRI) protocol for quantifying the optic nerve diameter (OND) as a measure of axonal loss in the optic nerve. METHODS: Included in the study was one eye each from 47 subjects, of whom 9 had no eye disease, 16 had preperimetric glaucoma, 11 had a glaucomatous mean visual field defect of <10 dB and 11 of >10 dB. Each subject underwent automated perimetry, scanning laser polarimetry, optic coherence tomography, scanning laser tomography, and ultrafast high-resolution MRI at 3 T. OND was determined 5, 10, and 15 mm behind the eye with a half Fourier-acquired single-shot turbo spin-echo (HASTE)-sequence requiring 1.5 seconds of data acquisition time per slice and providing a spatial resolution of 0.11 mm. A multiple linear regression model was applied to determine correlations (r) among the different techniques. RESULTS: The correlation (r) was <0.37 for OND measurements taken 5 mm behind the eye. At 10 mm behind the eye, r increased to 0.57 and was statistically significant in four out six instances. In the orbital apex 15 mm behind the eye, r reached a maximum of 0.80 and was statistically significant in all instances. OND correlated best with the retinal nerve fiber layer thickness measured by optic coherence tomography. CONCLUSIONS: Retina- or optic nerve head-related surrogate markers for axonal content correlated closely with the OND, although only when it was measured in the orbital apex. High-resolution MRI using an ultrafast HASTE-sequence at 3 T proved useful for OND quantification and may be a valuable asset in future neuroprotection trials.
机译:目的:评估一种新颖的磁共振成像(MRI)协议,用于量化视神经直径(OND),以量度视神经轴突损失。方法:该研究包括来自47名受试者的每只眼睛一只,其中9名没有眼部疾病,16名患有围前期青光眼,11名患有青光眼平均视野缺损<10 dB,11名≥10 dB。每个受试者在3 T时进行自动视野检查,扫描激光旋光检查,光学相干断层扫描,扫描激光断层扫描和超快高分辨率MRI。用半个傅里叶获取的单次成像确定OND在眼后5、10和15 mm涡轮自旋回波(HASTE)序列,每个切片需要1.5秒的数据采集时间,并提供0.11 mm的空间分辨率。应用多元线性回归模型来确定不同技术之间的相关性(r)。结果:在距眼后5毫米处进行OND测量的相关性(r)<0.37。在眼后10毫米处,r增加到0.57,在六分之四的情况下具有统计学意义。在眼后15 mm的眶尖,r达到最大值0.80,在所有情况下均具有统计学意义。通过光学相干断层扫描测量,OND与视网膜神经纤维层厚度最相关。结论:视网膜或视神经头相关的轴突含量替代标志物与OND密切相关,尽管仅在眶尖进行测量。在3 T处使用超快HASTE序列进行的高分辨率MRI被证明对OND定量有用,并且可能是未来神经保护试验中的宝贵资产。

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