Fan Yangyi, Shen Ming, Huo Yang, Gao Xuguang, Li Chun, Zheng Ruimao, Zhang Jun
Department of Neurology, Peking University People's Hospital, Beijing, China.
Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing, China.
Front Aging Neurosci. 2021 Sep 8;13:698035. doi: 10.3389/fnagi.2021.698035. eCollection 2021.
Cerebral small vessel disease (cSVD) and neurodegeneration are the two main causes of dementia and are considered distinct pathological processes, while studies have shown overlaps and interactions between the two pathological pathways. Medial temporal atrophy (MTA) is considered a classic marker of neurodegeneration. We aimed to investigate the relationship of total cSVD burden and MTA on MRI using a total cSVD score and to explore the impact of the two MRI features on cognition. Patients in a memory clinic were enrolled, who underwent brain MRI scan and cognitive evaluation within 7 days after the first visit. MTA and total cSVD score were rated using validated visual scales. Cognitive function was assessed by using Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA) scales. Spearman's correlation and regression models were used to test (i) the association between MTA and total cSVD score as well as each cSVD marker and (ii) the correlation of the MRI features and cognitive status. A total of 312 patients were finally enrolled, with a median age of 75.0 (66.0-80.0) years and 40.7% (127/312) males. All of them finished MRI and MMSE, and 293 subjects finished MoCA. Of note, 71.8% (224/312) of the patients had at least one of the cSVD markers, and 48.7% (152/312) of them had moderate-severe MTA. The total cSVD score was independently associated with MTA levels, after adjusting for age, gender, years of education, and other vascular risk factors (OR 1.191, 95% CI 1.071-1.324, = 0.001). In regard to individual markers, a significant association existed only between white matter hyperintensities and MTA after adjusting for the factors mentioned above (OR 1.338, 95% CI 1.050-1.704, = 0.018). Both MTA and total cSVD score were independent risk factors for MMSE ≤ 26 (MTA: OR 1.877, 95% CI 1.407-2.503, < 0.001; total cSVD score: OR 1.474, 95% CI 1.132-1.921, = 0.004), and MoCA < 26 (MTA: OR 1.629, 95% CI 1.112-2.388, = 0.012; total cSVD score: OR 1.520, 95% CI 1.068-2.162, = 0.020). Among all the cSVD markers, microbleed was found significantly associated with MMSE ≤ 26, while no marker was demonstrated a relationship with MoCA < 26. Cerebral small vessel disease was related to MTA in patients of a memory clinic, and both the MRI features had a significant association with cognitive impairment.
脑小血管病(cSVD)和神经退行性变是痴呆的两个主要病因,被认为是不同的病理过程,然而研究表明这两种病理途径之间存在重叠和相互作用。内侧颞叶萎缩(MTA)被认为是神经退行性变的经典标志物。我们旨在使用cSVD总分研究MRI上cSVD总负担与MTA的关系,并探讨这两种MRI特征对认知的影响。招募了记忆门诊的患者,他们在首次就诊后7天内接受了脑部MRI扫描和认知评估。使用经过验证的视觉量表对MTA和cSVD总分进行评分。通过简易精神状态检查表(MMSE)和蒙特利尔认知评估量表(MoCA)评估认知功能。使用Spearman相关性和回归模型来检验:(i)MTA与cSVD总分以及每个cSVD标志物之间的关联;(ii)MRI特征与认知状态的相关性。最终共纳入312例患者,中位年龄为75.0(66.0 - 80.0)岁,男性占40.7%(127/312)。所有患者均完成了MRI和MMSE检查,293例受试者完成了MoCA检查。值得注意的是,71.8%(224/312)的患者至少有一项cSVD标志物,其中48.7%(152/312)有中度至重度MTA。在调整年龄、性别、受教育年限和其他血管危险因素后,cSVD总分与MTA水平独立相关(OR 1.191,95%CI 1.071 - 1.324,P = 0.001)。对于单个标志物,在调整上述因素后,仅白质高信号与MTA之间存在显著关联(OR 1.338,95%CI 1.050 - 1.704,P = 0.018)。MTA和cSVD总分均为MMSE≤26的独立危险因素(MTA:OR 1.877,95%CI 1.407 - 2.503,P < 0.001;cSVD总分:OR 1.474,95%CI 1.132 - 1.921,P = 0.004),以及MoCA < 26的独立危险因素(MTA:OR 1.629,95%CI 1.112 - 2.388,P = 0.012;cSVD总分:OR 1.520,95%CI 1.068 - 2.162,P = 0.020)。在所有cSVD标志物中,微出血与MMSE≤26显著相关,而没有标志物与MoCA < 26相关。在记忆门诊患者中,脑小血管病与MTA相关,且这两种MRI特征均与认知障碍显著相关。