Structural and functional hippocampal alterations in Multiple sclerosis and neuromyelitis optica spectrum disorder

Author:

Zheng Fenglian1,Li Yuxin2,Zhuo Zhizheng1,Duan Yunyun1,Cao Guanmei1ORCID,Tian Decai3,Zhang Xinghu3,Li Kuncheng4,Zhou Fuqing5,Huang Muhua5,Li Haiqing2,Li Yongmei6,Zeng Chun6,Zhang Ningnannan7,Sun Jie7,Yu Chunshui7,Han Xuemei8,Hallar Sven9,Barkhof Frederik10,Liu Yaou1

Affiliation:

1. Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

2. Department of Radiology, Huashan Hospital, Fudan University, Shanghai, China

3. Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

4. Department of Radiology, Xuanwu Hospital, Capital Medical University, Beijing, China

5. Department of Radiology, The First Affiliated Hospital, Nanchang University, Nanchang, China/Neuroimaging Lab, Jiangxi Province Medical Imaging Research Institute, Nanchang, China

6. Department of Radiology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China

7. Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin, China

8. Department of Neurology, China-Japan Union hospital of Jilin University, Changchun, China

9. Centre d’Imagerie Médicale de Cornavin, Geneva, Switzerland/Department of Surgical Sciences, Radiology, Uppsala University, Sweden/Faculty of Medicine of the University of Geneva, Switzerland/Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China

10. Department of Radiology and Nuclear Medicine, Amsterdam UMC, Amsterdam, The Netherlands/Queen Square Institute of Neurology and Center for Medical Image Computing, University College London, London, UK

Abstract

Background: Hippocampal involvement may differ between multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD). Objective: To investigate the morphometric, diffusion and functional alterations in hippocampus in MS and NMOSD and the clinical significance. Methods: A total of 752 participants including 236 MS, 236 NMOSD and 280 healthy controls (HC) were included in this retrospective multi-center study. The hippocampus and subfield volumes, fractional anisotropy (FA) and mean diffusivity (MD), amplitude of low frequency fluctuation (ALFF) and degree centrality (DC) were analyzed, and their associations with clinical variables were investigated. Results: The hippocampus showed significantly lower volume, FA and greater MD in MS compared to NMOSD and HC ( p < 0.05), while no abnormal ALFF or DC was identified in any group. Hippocampal subfields were affected in both diseases, though subiculum, presubiculum and fimbria showed significantly lower volume only in MS ( p < 0.05). Significant correlations between diffusion alterations, several subfield volumes and clinical variables were observed in both diseases, especially in MS ( R = −0.444 to 0.498, p < 0.05). FA and MD showed fair discriminative power between MS and HC, NMOSD and HC (AUC > 0.7). Conclusions: Hippocampal atrophy and diffusion abnormalities were identified in MS and NMOSD, partly explaining how clinical disability and cognitive impairment are differentially affected.

Funder

national natural science foundation of china

Beijing Natural Science fund

Beijing Nova Program

Shanghai new star of Medical Court

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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