Frontiers in immunology · 2026
Microstructural white matter alterations and cognitive impairment in anti-NMDAR encephalitis: evidence from T1w/T2w ratio analysis.
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Tao Jinyu, Ding Shuang, Xiang Yayun, Zhu Qiyuan, Shi Zhuowei, Du Run, Li Yongmei, Zeng Chun
Аннотация
OBJECTIVE: Anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis often causes cognitive impairment, yet conventional MRI lacks sensitivity to detect related microstructural changes. This study aimed to investigate T1-weighted/T2-weighted (T1w/T2w) ratios alterations in normal-appearing white matter (NAWM) and their relationship with cognitive function in patients with anti-NMDAR encephalitis, including a 12-month longitudinal follow-up.
METHODS: Fifty-nine patients with anti-NMDAR encephalitis (31 with mild cognitive impairment (MCI), 28 with no cognitive impairment (NCI)) and 34 healthy controls (HCs) underwent 3.0T whole-brain MRI and comprehensive neuropsychological assessments, including the Montreal Cognitive Assessment (MoCA), Mini-Mental State Examination (MMSE), and domain-specific tests for attention-executive function, memory, and visuospatial reasoning. T1w/T2w ratios were calculated for globel NAWM and multiple major white matter (WM) tracts. Eighteen MCI patients were followed longitudinally for 12 months to evaluate changes in T1w/T2w ratios and cognitive performance over time.
RESULTS: Compared with NCI patients and HCs, MCI patients exhibited significantly reduced T1w/T2w ratios in global NAWM (P < 0.001) and multiple WM tracts, including the corpus callosum, fornix, left hippocampal cingulum, and right hippocampal cingulum (all P < 0.05). Lower ratios were significantly associated with worse global cognition (r = 0.364, P = 0.023), memory (r = 0.336, P = 0.023), and visuospatial reasoning performance (r = 0.397, P = 0.005). In the 18 MCI patients with 12-month follow-up, increased T1w/T2w ratios in the fornix and hippocampal cingulum (both P = 0.009) were accompanied by significant improvements in visuospatial reasoning and memory functions.
CONCLUSION: T1w/T2w ratios derived from routine MRI provide a sensitive, clinically feasible biomarker for detecting NAWM microstructural damage in anti-NMDAR encephalitis. Longitudinal changes in these ratios may parallel cognitive improvement, and these preliminary findings support further investigation of this metric as an imaging biomarker, independent cohorts.
METHODS: Fifty-nine patients with anti-NMDAR encephalitis (31 with mild cognitive impairment (MCI), 28 with no cognitive impairment (NCI)) and 34 healthy controls (HCs) underwent 3.0T whole-brain MRI and comprehensive neuropsychological assessments, including the Montreal Cognitive Assessment (MoCA), Mini-Mental State Examination (MMSE), and domain-specific tests for attention-executive function, memory, and visuospatial reasoning. T1w/T2w ratios were calculated for globel NAWM and multiple major white matter (WM) tracts. Eighteen MCI patients were followed longitudinally for 12 months to evaluate changes in T1w/T2w ratios and cognitive performance over time.
RESULTS: Compared with NCI patients and HCs, MCI patients exhibited significantly reduced T1w/T2w ratios in global NAWM (P < 0.001) and multiple WM tracts, including the corpus callosum, fornix, left hippocampal cingulum, and right hippocampal cingulum (all P < 0.05). Lower ratios were significantly associated with worse global cognition (r = 0.364, P = 0.023), memory (r = 0.336, P = 0.023), and visuospatial reasoning performance (r = 0.397, P = 0.005). In the 18 MCI patients with 12-month follow-up, increased T1w/T2w ratios in the fornix and hippocampal cingulum (both P = 0.009) were accompanied by significant improvements in visuospatial reasoning and memory functions.
CONCLUSION: T1w/T2w ratios derived from routine MRI provide a sensitive, clinically feasible biomarker for detecting NAWM microstructural damage in anti-NMDAR encephalitis. Longitudinal changes in these ratios may parallel cognitive improvement, and these preliminary findings support further investigation of this metric as an imaging biomarker, independent cohorts.