Evidence map›Paper›PMID 41204096›Full record

ArticleBMC medical imaging2025

Neurite orientation dispersion and density imaging reveals microstructural damage in moyamoya disease: a study based on tract- and gray-based spatial statistics.

Jia-Yan Shi, Shao-Peng Zhuang, Zi-Wei Cai, Shun-Fei Xu, Ying Tang, Hui-Wei Huang, Jian-Qi Li, Xian-Kun Tu, Hua-Jun Chen

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Article in BMC medical imaging, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Jia-Yan Shi *Department of Radiology, Fujian Medical University Union Hospital, Fuzhou, 350001, China.
Shao-Peng Zhuang *Department of Radiology, Fujian Medical University Union Hospital, Fuzhou, 350001, China.
Zi-Wei Cai *Department of Radiology, Fujian Medical University Union Hospital, Fuzhou, 350001, China.
Shun-Fei Xu *Department of Neurosurgery, Fujian Medical University Union Hospital, Fuzhou, 350001, China.
Ying Tang *Shanghai key Laboratory of Magnetic resonance, Institute of Magnetic Resonance and Molecular Imaging in Medicine, School of Physics and Electronic Science, East China Normal University, Shanghai, 200062, China.
Hui-Wei HuangDepartment of Radiology, Fujian Medical University Union Hospital, Fuzhou, 350001, China. 18859980147@163.com.
Jian-Qi LiShanghai key Laboratory of Magnetic resonance, Institute of Magnetic Resonance and Molecular Imaging in Medicine, School of Physics and Electronic Science, East China Normal University, Shanghai, 200062, China. jqli@phy.ecnu.edu.cn.
Xian-Kun TuDepartment of Neurosurgery, Fujian Medical University Union Hospital, Fuzhou, 350001, China. unionnstu@hotmail.com.
Hua-Jun ChenDepartment of Radiology, Fujian Medical University Union Hospital, Fuzhou, 350001, China. chj0075@126.com.

Funding

Excellent Young Scholars Cultivation Project of Fujian Medical University Union Hospital 2022XH040Natural Science Foundation of Fujian Province no. 2024J01599
6 · The paper itself

Abstract

background and purposeThis study aims to comprehensively assess microstructural abnormalities in both gray matter (GM) and white matter (WM) in patients with moyamoya disease (MMD) using neurite orientation dispersion and density imaging (NODDI). The analysis integrates GM-based and tract-based spatial statistics (GBSS and TBSS, respectively).

methodsDiffusion-weighted imaging was performed on 26 healthy controls and 15 patients with MMD. NODDI metrics-including the neurite density index (NDI), orientation dispersion index (ODI), and isotropic volume fraction (ISOVF)-as well as diffusion tensor imaging (DTI) parameters-fractional anisotropy and mean diffusivity (MD)-were estimated and compared using GBSS and TBSS approaches.

resultsThe analysis revealed significant microstructural alterations in both GM and WM among patients with MMD. In GM, reduced ODI was observed in multiple regions, including areas associated with the default mode network, executive control network, visual cortex, auditory cortex, sensorimotor cortex, and insula. In WM, decreased NDI and increased ISOVF were identified, predominantly in the corpus callosum, corona radiata, and bilateral frontal and parietal lobes. Although both DTI and NODDI metrics showed similar spatial distribution patterns of WM changes, the alterations detected by NODDI were more widespread. This suggests that NODDI may provide superior sensitivity for identifying microstructural changes associated with MMD.

conclusionThe integration of NODDI with GBSS and TBSS enhances the detection of cerebral microstructural alterations in MMD. These findings highlight the potential of NODDI-based metrics as valuable imaging biomarkers for improving diagnostic accuracy in MMD.

Indexed as

Diffusion Tensor ImagingGray MatterMoyamoya DiseaseNeuritesWhite MatterAdolescentAdultAnisotropyCase-Control StudiesDiffusion Magnetic Resonance ImagingFemaleHumansMaleMiddle AgedYoung AdultGlobal-based spatial statisticsMicrostructureMoyamoyaNeurite orientation dispersion and density imagingTract-based spatial statistics

Identifiers

PMID41204096
PMCPMC12595892

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.