Linying Guo1 and Zuohua Tang1
1Fudan University, Eye & ENT Hospital, Shanghai, China
Synopsis
Keywords: Head & Neck/ENT, Head & Neck/ENT
Motivation: The underlying structural pathophysiology of visual white matter degeneration in primary open-angle glaucoma (POAG) remains incompletely understood.
Goal(s): To characterize macro- and micro-structural abnormalities in the optic tract and optic radiation of POAG by multiple morphology and diffusion metrics derived from diffusion spectrum imaging(DSI)
Approach: DSI was performed on 34 bilateral POAG patients and 25 healthy controls (HCs), and multiple morphology and diffusion metrics were calculated and compared.
Results: Significant differences emerged in morphology and diffusion metrics between POAG patients and HCs.
Impact: Our demonstration of multiple morphology and diffusion changes in POAG utilizing DS suggests the macro- and micro-structural white matter abnormalities, which could be used for assessing POAG degenetation
Introduction
Primary open-angle glaucoma (POAG)
has been recognized as a neurodegenerative disease with structural
abnormalities in extraretinal visual white matter, particularly in the optic
tract (OT) and the optic radiation (OR), but the underlying structural
pathophysiology is not fully understood [1]. Diffusion
MRI is the primary non-invasive modality for quantifying the structural
neurodegeneration of glaucoma visual white matter and diffusion spectrum
imaging (DSI) is a high angular resolution dMRI technique using probabilistic
tractography, which can accurately depict the complex architecture of visual
pathway and derive DTI-, NODDI- and MAP metrics through one single acquisition
[2-4]. However,
these metrics have not been applied on POAG. The objective of the current study
was to comprehensively evaluate the he macro- and micro-structural
abnormalities of OR and OT in POAG by multiple DSI-derived morphology and
diffusion metrics.Methods
We conducted a prospective DSI
study involving 34 bilateral POAG patients and 25 healthy controls (HCs). We
derived and compared multiple morphology metrics, including volume, area,
length, and shape metrics, as well as diffusion metrics such as diffusion
tensor imaging (DTI), mean apparent propagator (MAP), and neurite orientation
dispersion and density imaging (NODDI) metrics of the OT and OR. Statistical
comparisons employed t-test or Mann-Whitney U test. Logistic regression models
were constructed to differentiate between POAG patients and HCs using these MRI
metrics.Results
Significant differences
emerged in morphology and diffusion metrics. In morphology, POAG patients
exhibited length and shape changes, including a reduced span in the OR and a
decreased span, along with a higher curl, in the OT compared to HCs (all p <
0.05). Regarding diffusion, POAG patients demonstrated decreased DTI_FA_Mean
and MAP_RTAP_Mean in the OR, while showing lower DTI_FA_Mean and higher
DTI_RD_Mean, MAP_RTAP_Mean, MAP_MSD_Mean, and NODDI_ODI_Mean in the OT (all p
< 0.05). The logistic regression models, incorporating these MRI metrics,
effectively discriminated between POAG patients and HCs, achieving AUCs
of 0.860 for the OR and 0.888 for the OT.Discussion
Our findings revealed
distinctive changes in the shape and length features, indicative of macro-structural
degeneration in the OT and OR, which, to our knowledge, have not been
previously reported. Moreover, we explored multiple diffusion metrics to
examine micro-structural pathology, with the inclusion of MAP metrics for the
first time, which demonstrated superior sensitivity compared to conventional
DTI metrics. Furthermore, the
study indicated that OR appeared to be less severely affected than OT. These
results enhance our understanding of the visual white matter degeneration in
POAG patients.Conclusions
DSI-derived morphology and
diffusion metrics offer valuable insights into the macro- and micro-structural
white matter degeneration in the OT and OR of POAG. Furthermore, the OR may
exhibit less severe degeneration compared to the OT.Acknowledgements
This work was supported by the National Natural Science
Foundation of China
(Grant No. 81871341, 82271945, 81430007).References
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