定量磁化率图
苍白球
基底神经节
壳核
病理
磁共振成像
伏隔核
核磁共振
尾状核
丘脑
磁化率加权成像
医学
神经科学
化学
抗磁性
磁化率
生物
疾病
白质
基础(医学)
中枢神经系统
认知功能衰退
大脑定位
作者
Y Yuan,Shuai Jiang,Y. Wang,Huilou Liang,Marta Lancione,Michela Tosetti,Boyan Yan,Yuying Yan,Mangmang Xu,Siyi Li,Jiaxin Zeng,Tang Ll,Pengfei Peng,Su Lui,J K Sun,Bo Wu
标识
DOI:10.1177/0271678x261473382
摘要
Susceptibility alterations in deep gray matter (DGM) across clinical stages of cerebral small vessel disease (CSVD) remain unclear. In this case-control study, we used 7-tesla magnetic resonance imaging quantitative susceptibility mapping (QSM) with source separation (APART-QSM) to characterize stage-related changes in normal controls, preclinical CSVD, and symptomatic CSVD. Compared with controls, CSVD showed increased QSM in the basal ganglia, particularly the putamen and globus pallidus, whereas small-magnitude QSM reductions were observed in selected thalamic and amygdalar subregions (all P < 0.05). Source separation revealed that basal ganglia abnormalities were mainly associated with increased paramagnetic components, whereas some thalamic alterations may involve increased diamagnetic components, suggesting distinct susceptibility contributions. Lower MoCA scores were associated with higher QSM and paramagnetic values in the globus pallidus, as well as higher diamagnetic values across the thalamus, putamen, and nucleus accumbens (all P < 0.05). Notably, right anterior globus pallidus QSM discriminated symptomatic CSVD from controls with the highest accuracy (AUC = 0.818). These findings reveal DGM susceptibility patterns associated with cognitive impairment, suggesting that 7T QSM and susceptibility source separation may provide complementary information for early CSVD characterization and future longitudinal evaluation.
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