慢性脑循环不全患者认知功能障碍的蒙特利尔认知评估及相关因素分析

Lin Zhang, Wenjing Dong, Jie Han, Zhe Wang, Dayong Sun, Xiaofei Ji, Ming Li, B. Zhang
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Results Age (p = 0.007, OR = 3.768, χ2 = 7.173), leukoaraiosis (p = 0.002, OR = 6.231, χ2 = 9.478), a history of hypertension (p = 0.021, OR = 3.078, χ2 = 5.307), a history of hyperlipidemia (p = 0.016, OR = 3.429, χ2 = 5.795), and the number of vascular risk factors (p = 0.019, χ2 = 9.921) were related to cognitive impairment by univariate analysis. Age (p = 0.070, OR = 2.689, 95% CI = 0.923 ± 7.837) and leukoaraiosis (p = 0.012, OR = 4.531, 95% CI = 1.401 ± 14.667) were significant by multivariate logistic regression analysis. Age (r = −0.585, p < 0.01) had a marked negative correlation with MoCA scores. There were significant differences in the MoCA subscale scores, including visuospatial and executive capacity (p < 0.01), attention and calculation (p < 0.01), and delayed recall (p < 0.01), in patients with different degrees of leukoaraiosis. Patients with CCCI had a higher incidence of cognitive impairment (78.4%). 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引用次数: 4

摘要

背景慢性脑循环不全(CCCI)是指导致脑血管病变的脑功能障碍。我们的目的是确定CCCI中与认知障碍相关的因素。方法对102例CCCI患者进行蒙特利尔认知评估(MoCA),分析认知功能障碍。根据MoCA评分将患者分为两组:(1)认知功能障碍组和(2)认知功能正常组。我们将临床信息与单变量和多变量logistic回归分析进行比较,确定了CCCI中与认知功能障碍相关的主要危险因素。结果单因素分析显示,年龄(p = 0.007, OR = 3.768, χ2 = 7.173)、白质变(p = 0.002, OR = 6.231, χ2 = 9.478)、高血压史(p = 0.021, OR = 3.078, χ2 = 5.307)、高脂血症史(p = 0.016, OR = 3.429, χ2 = 5.795)、血管危险因素数量(p = 0.019, χ2 = 9.921)与认知功能障碍相关。多因素logistic回归分析显示,年龄(p = 0.070, OR = 2.689, 95% CI = 0.923±7.837)、白质病变(p = 0.012, OR = 4.531, 95% CI = 1.401±14.667)具有显著性差异。年龄与MoCA评分呈显著负相关(r = - 0.585, p < 0.01)。不同程度白质病变患者的MoCA亚量表得分,包括视觉空间和执行能力(p < 0.01)、注意和计算能力(p < 0.01)、延迟回忆能力(p < 0.01),差异均有统计学意义。CCCI患者认知功能障碍发生率较高(78.4%)。结论视觉空间和执行能力、延迟回忆和语言功能的改变是CCCI的认知表现。年龄和白质病变对认知障碍发病率的影响最大,并可加重认知障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Montreal cognitive assessment and analysis of related factors for cognitive impairment in patients with chronic cerebral circulation insufficiency
Background Chronic cerebral circulation insufficiency (CCCI) refers to cerebral dysfunctions that lead to cerebral vascular pathological changes. Our aim is to identify factors related to cognitive impairment in CCCI. Methods CCCI patients (n = 102) were assessed with the Montreal cognitive assessment (MoCA) to analyze cognitive impairment. Patients were divided into two groups according to MoCA scores: (1) cognitive dysfunction and (2) normal cognitive function. We compared the clinical information with univariate and multivariate logistic regression analyses and identified major risk factors related to cognitive impairment in CCCI. Results Age (p = 0.007, OR = 3.768, χ2 = 7.173), leukoaraiosis (p = 0.002, OR = 6.231, χ2 = 9.478), a history of hypertension (p = 0.021, OR = 3.078, χ2 = 5.307), a history of hyperlipidemia (p = 0.016, OR = 3.429, χ2 = 5.795), and the number of vascular risk factors (p = 0.019, χ2 = 9.921) were related to cognitive impairment by univariate analysis. Age (p = 0.070, OR = 2.689, 95% CI = 0.923 ± 7.837) and leukoaraiosis (p = 0.012, OR = 4.531, 95% CI = 1.401 ± 14.667) were significant by multivariate logistic regression analysis. Age (r = −0.585, p < 0.01) had a marked negative correlation with MoCA scores. There were significant differences in the MoCA subscale scores, including visuospatial and executive capacity (p < 0.01), attention and calculation (p < 0.01), and delayed recall (p < 0.01), in patients with different degrees of leukoaraiosis. Patients with CCCI had a higher incidence of cognitive impairment (78.4%). Conclusions Changes in visuospatial and executive capacity, delayed recall, and language function represent cognitive manifestations in CCCI. Age and leukoaraiosis have the strongest effects on cognitive impairment morbidity and can aggravate cognitive impairment.
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