长沙市缺血性脑卒中患者血管性认知功能障碍的现状与对策研究
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摘要
第一篇长沙市缺血性脑卒中患者血管性认知功能障碍的发生与分布
     目的:
     描述长沙市缺血性脑卒中患者的血管性认知功能障碍(VCI)、非痴呆型血管性认知功能障碍(VCIND)、血管性痴呆(VD)的患病率;描述长沙市缺血性脑卒中患者不同认知功能水平的人口学分布特征;为长沙市缺血性脑卒中患者VCI、VCIND、VD的流行病学调查提供基线数据;为长沙市VCI疾病库的建立提供资料;为相关的卫生政策制定提供科学数据。
     方法:
     采用整群随机抽样方法,对长沙市8个社区689例40岁及以上缺血性脑卒中患者进行长沙版蒙特利尔认知评估量表(长沙版MoCA)、简明精神状态检查量表(MMSE)、额叶功能评估量表(FAB)、韦氏逻辑记忆、日常生活活动量表(ADL)、临床痴呆评定量表(CDR)社会功能问卷(FAQ)、流调用抑郁自评量表(CES-D)、美国国立卫生院卒中量表(NIHSS)等量表的评估,参考美国国立神经疾病与卒中研究所和加拿大卒中网(NINDS/CNS)组织召开的血管性认知功能障碍统一标准专题研讨会中诊断指南中的方案进行诊断,根据NINDS-AIREN诊断标准及血管性认知功能损害专家指南中VCIND诊断标准筛查出血管性认知功能障碍者,并通过自主设计的问卷调查研究对象的人口学特征及VCI可能的各相关因素。
     结果:
     1.长沙市40岁以上缺血性脑卒中VCI的患病率为41.8%,其中VCIND为32.1%,VD为9.7%;男性中VCI的患病率为39.3%,其中VCIND为29.2%,VD为10.1%;女性中VCI的患病率为45.2%,其中VCIND为36.1%,VD为9.1%。
     2.缺血性脑卒中后VCI患者在不同年龄(x2=40.745,P=0.000)、不同职业(x2=24.359,P=0.000)、不同文化程度(x2=238.565,P=0.000)、不同婚姻状况(x-=9.206,P=0.010)、不同居住状况(x2=24.359,P=0.000)中的分布差异有统计学意义;而在不同性别(x2=3.686,P=0.158)中的分布差异无统计学意义。
     3.缺血性脑卒中后认知正常组、VCIND组及VD组在ADL(F=65.601,P=-0.000)、FAQ(F=78.305,P=-0.000)、CES-D(F=5.306,P=0.006)、NIHSS (F=12.340, P=0.000)的得分比较,均有统计学意义。
     结论:
     1.长沙市40岁以上缺血性脑卒中患者中VCI的患病率为41.8%,其中VCIND的患病率为32.1%,VD患病率为9.7%。
     2.长沙市40岁以上缺血性脑卒中后VCI患者在高龄、体力劳动、低文化程度、单身和独居者中分布较多。
     第二篇长沙市缺血性脑卒中患者血管性认知功能障碍的影响因素研究
     目的:
     从社会人口学、疾病史、脑卒中相关临床表现、神经影像学资料、行为生活方式等维度来探讨长沙市缺血性脑卒中患者VCI的影响因素,为缺血性脑卒中患者VCI的防治提供科学依据。
     方法:
     采用整群随机抽样方法,对长沙市8个社区689例40岁及以上缺血性脑卒中患者进行长沙版MoCA、MMSE、FAB、韦氏逻辑记忆、ADL、CDR等量表的评估,并进行问卷调查。参考美国国立神经疾病与卒中研究所和加拿大卒中网(NINDS/CNS)组织召开的血管性认知功能障碍统一标准专题研讨会中诊断指南中的方案进行诊断,根据NINDS-AIREN诊断标准和血管性认知功能损害专家指南中诊断标准筛查出血管性认知功能障碍者,将缺血性脑卒中后认知正常者作为对照,采用单一维度非条件logistic回归模型对包括社会人口学、疾病史、脑卒中相关临床表现、神经影像学资料、行为生活方式等维度42个变量进行分析,筛选出有统计学意义的变量。对有统计学意义的变量进行共线性诊断,确认这些变量不存在共线性时,再对这些变量进行多维度非条件logistic回归分析。
     结果:
     1.通过单一维度非条件logistic回归分析,从42个变量中分别筛选出16个有统计学意义的变量作为VCIND的影响因素和17个有统计学意义的变量作为VD的影响因素。
     2.共线性诊断结果发现,VCIND及VD有统计学意义的变量之间均不存在明显的共线性关系。
     3.通过多维度非条件logistic回归分析,发现有11个变量进入VCIND回归方程,其中高龄(OR=1.256)、侧脑室白质变性评分高(OR=2.015)、大血管病变(OR=2.088)、大量饮酒(OR=3.334)、缺乏业余爱好(OR=5.941)、睡眠时间长(OR=1.880)是缺血性脑卒中患者VCIND发生的危险因素,而文化程度高(OR=0.388)、体力劳动(OR=0.478)、少量饮酒(OR=0.053)、定期体检(OR=0.436)、丰富膳食纤维摄入(OR=0.178)、喝牛奶(OR=0.266)为VCIND的保护因素;在VD影响因素分析时,有9个变量进入回归方程,其中独居(OR=22.235)、高脂血症(OR=33.357)、短暂性脑缺血发作(TIA)(OR=4.624)、脑卒中家族史(OR=14.183)、脑萎缩(OR=26.445)、饮食不规律(OR=18.561)、高脂饮食(OR=3.400)是缺血性脑卒中患者VD发生的危险因素,而文化程度高(OR=0.253)、素食为主(OR=0.268)为VD的保护因素。
     结论:
     1.年龄、侧脑室白质变性、大血管病变、大量饮酒、缺乏业余爱好、睡眠时间长是缺血性脑卒中患者VCIND的危险因素;而文化程度高、体力劳动、少量饮酒、定期体检、丰富膳食纤维摄入、喝牛奶为VCIND的保护因素。
     2.独居、高脂血症、TIA、脑卒中家族史、脑萎缩、饮食不规律、高脂饮食是缺血性脑卒中患者VD的危险因素,而文化程度高、素食为主为VD的保护因素。
     第三篇长沙市公众对血管性认知功能障碍的认知度调查
     目的:
     通过调查长沙公众对VCI的认知度,为VCI防治路径的建立提供依据。
     方法:
     采用整群随机抽样方法,对长沙市8个社区689例40岁及以上缺血性脑卒中患者进行长沙版MoCA、MMSE、FAB、韦氏逻辑记忆、ADL、CDR等量表的评估。参考美国国立神经疾病与卒中研究所和加拿大卒中网(NINDS/CNS)所建议的诊断指南进行认知评估,根据NINDS-AIREN诊断标准和血管性认知功能损害专家指南中诊断标准进行认知诊断。同时,分别对患者及其照料者、所在社区基层医务工作者以及随机抽取的一家综合性医院的医务工作者采用自主设计的问卷进行VCI的认知度及态度两个方面的调查。采用描述性分析、t检验或单因素方差分析法对公众VCI的知晓度、早期症状的识别率、就诊情况及其经济承受能力、医务人员对VCI的诊治能力等进行分析。
     结果:
     1、公众对VCI的基本知晓率仅为30.9%,其中患者为24.7%,照料者为29.3%,基层医师为61.8%,专科医师为100.0%;公众对VCI的早期症状的识别率仅为22.8~28.9%,其中患者为16.3%-22.6%,照料者为23.3%-31.6%,基层医师为38.2%-47.4%,专科医师为67.4%-74.4%;16.2%的患者和照料者对VCI存在偏见,占知晓人群的52.4%。
     2、各研究人群的认识度、态度、总得分由大到小排列均为:患者>照料者>医师,且其差异均有统计学意义,(P<0.05);专业意义提示医师对VCI的认知度较患者、照料者为高。
     3、不同的医师其认识度、态度、总得分由大到小排列均为:基层医师>专科医师。其差异均有统计学意义,(P<0.05);专业意义提示专科医生的认知度及态度比基层医生为好。
     结论:
     1、普通公众对VCI认知度不够,甚至对VCI存在偏见,这可能是病人及照料者就诊意识不强、诊断滞后、疗效欠佳等重要原因。
     2、医务人员对VCI认识不足,这可能是影响其早期识别、及时诊治的重要原因。
     3、基层医师与专科医师对VCI的认识程度不同,这可能是双向转诊困难、VCI治疗的依从性低,以及不能及时反馈治疗效果的重要原因。
     第四篇缺血性脑卒中患者血管性认知功能障碍的防治对策
     目的:
     根据长沙市缺血性脑卒中患者血管性认知功能障碍的人口学分布特征、影响因素以及公众对其认知度和态度的研究结果,探讨VCI的防治策略,为相关卫生政策的制定提供科学数据。
     方法:
     综合目前已完成的研究成果:长沙市缺血性脑卒中患者血管性认知功能障碍的人口学分布特征、影响因素以及公众对其认知度和态度,发现目前长沙市缺血性脑卒中患者VCI的防治现状及存在的如下问题:1、缺血性脑卒中患者的VCI患病率高达41.8%;2、VCI的影响因素分为危险因素和保护性因素,通过增强保护因素,减少危险因素等措施,VCI是可以有效的被防治的;3、目前公众对VCI的认知度低下,从多个环节严重地影响了VCI的有效防治。根据上述情况,提出相应的VCI防治策略,并建立VCI的防治路径。
     对策:
     1、加强宣传,提高公众意识。
     2、建立VCI患者的护理培训机构,消除照料者在对VCI患者的照料过程中出现的不良情绪及顾虑。
     3、提高基层医务工作者的医疗水平,规范化全科医生的培训,确实落实双向转诊制度。
     4、加强VCI专业技术人才培养,推进VCI相关的基础研究工作。
     5、建立VCI信息监测体系和居民健康档案。
     6、建议政府加大扶持力度,增加对VCI防治工作的投入。
     7、建立VCI防治路径。
Part I Cross-sectional Study on Vascular Cognitive Impairment after Ischemic Stroke in Changsha
     Objective:
     To describe the prevalence rate of vascular cognitive impairment (VCI)、vascular cognitive impairment non-dementia (VCIND) and vascular dementia (VD) among the patients with ischemic stroke and to describe the demographic distribution characteristics among the patients with different cognition status after ischemic stroke in Changsha, so as to provide baseline data for further studies on these diseases and to establish VCI library in the same area which can contribute for the government to make the associated health policies in Changsha.
     Methods:
     Stratified cluster random sampling method was performed and689patients with both ischemic stroke and his/her age being over40from8communities in Changsha were involved in this study. All subjects had accepted the following neuropsychological assessments:Montreal Cognitive Assessment-Changsha version (MoCA-CS), Mini-Mental State Examination (MMSE), Frontal Assessment Battery-Changsha version (FAB-CS), logical memory from Chinese revised Wechsler Memory Scale (WMS-RC), Activity of Daily Living Scale (ADL), Clinical Dementia Rating (CDR), Functional Activeities (FAQ), Center for Epidemiological Survey (CES-D), National Institute of Health stroke (NIHSS), etc. The criteria of diagnosis were as following:the National Institute of Neurological Disorders and Stroke-Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards, the NINDS-AIREN criteria. Additionally, Self-designed questionnaires were involved in analysing the demographic characteristics and risk factors of VCI.
     Results:
     1. The prevalence rate of VCI among ischemic stroke patients (=40years old) in Changsha was41.8%, which included that of VCI-ND was32.1%and that of VD was9.7%. To male, the prevalence rate of VCI was39.3%, which included that of VCI-ND was29.2%and that of VD was10.1%; To female, the prevalence rate of VCI was45.2%, which included that of VCI-ND was36.1%and that of VD was9.1%.
     2. The VCI distribution of patients with ischemic stroke was significantly different with age(χ2=40.745, P=0.000), occupations (χ2=24.359, P=0.000), educational level (χ2=238.565, P=0.000), marital status(χ2=9.206, P=0.010), habitation status (χ2=24.359, P=0.000), but not significantly different with gender(χ2=3.686, P=0.158).
     3. It was statistically significant that The score of ADL (F=65.601, P=0.000), FAQ (F=78.305, P=0.000), CES-D (F=5.306, P=0.006), NIHSS (F=12.340, P=0.000) among the patients with ischemic stroke in cognitive normal group, VCIND group and VD group.
     Conclusion:
     1. The prevalence rate of VCI among ischemic stroke patients (=40years old) in Changsha was41.8%, which included that of VCI-ND was32.1%and that of VD was9.7%.
     2. The VCI distribution of patients with ischemic stroke was significantly different with age, occupations, educational level, marital status, habitation status, but not significantly different with gender.
     Part Ⅱ Study on the Relevant Influencing Factors of Vascular Cognitive Impairment of the Patients with Ischemic Stroke in Changsha
     Objective:
     To explore the relevant influencing factors of vascular cognitive impairment (VCI) of the patients with ischemic stroke in Changsha as follows:demography, disease history, relevant clinical manifestation of stroke, neuroimaging data, personal living habits, to offer the data for preventing the occurrence of VCI after ischemic stroke.
     Methods:
     Stratified cluster random sampling method was performed and689patients with both ischemic stroke and his/her age being over40from8communities in Changsha were involved in this study. All subjects had accepted the following neuropsychological assessments:MoCA-CS, MMSE, FAB-CS, WMS-RC, ADL, CDR, etc. The criteria of diagnosis were as following:the National Institute of Neurological Disorders and Stroke-Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards, the NINDS-AIREN criteria. All participants were divided into two groups by the diagnosis as follows:the VCI group (including the patients with either VCI-ND or VD) and Control group (including the patients without cognitive imparement). The single factor unconditioned logistic regression analysis was performed to analyze the effects of42different variables from the following aspects (demography, disease history, relevant clinical manifestation of stroke, neuroimaging data, personal living habits) on the occurrence of VCI after ischemic stroke. Collinearity diagnostics was preformed among the variables with statistical significant by the single factor analysis, multi-factor unconditioned logistic regression analysis was done on the variables without any collinearity, to find the independent influencing factors of VCI after ischemic stroke.
     Results:
     1. The results of single factor unconditioned logistic regression analysis showed that,16statistical significant variables in the total42 variables could be selected as influencing factors of VCI-ND, but17in that could be selected as influencing factors of VD.
     2. The results of collinearity diagnostics showed that, there was no collinearity existed in the statistical significant variables of VCI-ND, so was VD.
     3. The results of multi-factor unconditioned logistic regression analysis showed that, there were12variables entered the regression equation of VCI-ND. Among these variables, advanced age (OR=1.256), high scores of leukoaraiosis in periventricular and deep white matter areas (OR=2.015), existing large vessel lesions (OR=2.088), a large amount of alcohol taking (OR=3.334), lack of hobbies (OR=5.941), long sleeping time (OR=1.880) were risk factors of VCI-ND. While, high educational level (OR=0.388), physical labour (OR=0.478), a small amount of alcohol taking (OR=0.053), regular physical examination (OR=0.436), rich in dietary fiber intake (OR=0.178), drinking milk (OR=0.266) were protective factors of VCI-ND. And there were9variables entered the regression equation of VD. Among them, Living alone (OR=22.235), hyperlipidemia (OR=33.357), TIA (OR=4.624), family history of stroke (OR=14.183), brain atrophy (OR=26.445), eating disorders (OR=18.561), high-fat diet (OR=3.400) were risk factors of VD after ischemic stroke, While, high educational level (OR=0.253), mainly vegetarian diet (OR=0.268) were protective factors of VD after ischemic stroke.
     Conclusions:
     1. Age, high scores of leukoaraiosis in periventricular and deep white matter areas, existing large vessel lesions, a large amount of alcohol taking, lack of hobbies, sleep for a long time were risk factors of VCI-ND after ischemic stroke, and high education level, manual labor, a small amount of alcohol taking, regular physical examination, rich in dietary fiber intake, drinking milk were protective factors of VCI-ND after ischemic stroke.
     2. Living alone, hyperlipidemia, TIA, family history of stroke, brain atrophy, eating disorders, high-fat diet were risk factors of VD after ischemic stroke, and high education level, mainly vegetarian diet were protective factors of VD after ischemic stroke.
     Part III Investigating the Public Awareness of Vascular Cognitive Impairment in Changsha
     Objective:
     Through investigating the public awareness of vascular cognitive impairment (VCI), to provide the basis for the establishment of the VCI control system.
     Methods:
     Stratified cluster random sampling method was performed and689patients with both ischemic stroke and his/her age being over40from8communities in Changsha were involved in this study. All subjects had accepted the following neuropsychological assessments:MoCA-CS, MMSE, FAB-CS, ADL, CDR, etc. The criteria of diagnosis were as following:the National Institute of Neurological Disorders and Stroke-Canadian Stroke Network Vascular Cognitive Impairment Harmonization Standards, the NINDS-AIREN criteria. Self-designed questionnaires were involved in analysing both the awareness of VCI and the attitudes to VCI, investigating subjects are as follows:patients and their caregivers, doctors from communities referred above, doctors from one of complexed hospitals chosen randomly in Changsha. It was described that public awareness, diagnosis of early symptoms, visiting doctors, paying for VCI, and doctors'diagnosis abilities of VCI by T test and one-way ANOVA.
     Results:
     1.The public basic awareness of the VCI was Only30.9%, Patient was24.7%, caregivers was29.3%, Grass-roots physicians was61.8%, professional physicians was100.0%; public recognition rate of early symptoms of VCI was22.8%-28.9%, patients was16.3%-22.6%, caregivers was23.3%-31.6%, Grass-roots physicians was38.2%-47.4%professional physicians was67.4%-74.4%;16.2%of the public had discrimination against VCI.
     2. Awareness score, attitude score and total score of different groups were descending as following:patients>caregivers>physicians, and the differences were statistically significant (P<0.05); Professional significance prompted that physician's recognition of VCI were better than patients and caregivers.
     3. Awareness score, attitude score and total score of different physicians were descending as following:grass-roots physicians> professional physicians, and the differences were statistically significant (P<0.05); Professional significance prompted that professional physician's recognition and attitude for VCI were better than grass-roots physicians.
     Conclusion:
     1. The general public awareness of VCI was not enough, even had a prejudice against VCI, which might be an important reason for poor treatment awareness of patients and carers, diagnosis lag and poor efficacy.
     2. Medical staff was lack of knowledge on VCI, which might affect its early recognition, timely diagnosis and treatment.
     3. The difference on awareness of VCI between grass-roots physicians and professional physicians might be an important reason,which caused both hard to realize the two-way referral and to do bad compliance and little feedback between doctors and patients.
     Part IV Prevention and control measures on Vascular Cognitive Impairment after Ischemic Stroke
     Objective:
     According to the population distribution characteristics, influence factors and the findings of public awareness and attitudes of vascular cognitive impairment after ischemic stroke in Changsha City, to explore the VCI control strategies and to provide scientific data for the formulation of health policy.
     Methods:
     Through integrating the present research results:the population distribution characteristics, influence factors and the public awareness and attitudes of vascular cognitive impairment after ischemic stroke in Changsha City, we found the control situation of VCI after ischemic stroke in Changsha City and the existence of the following questions:1The prevalence rate of VCI among ischemic stroke patients in Changsha was up to41.8%;2Influencing factors of VCI were divided into risk factors and protective factors, and then by enhancing protective factors and reducing risk factors, VCI can be effective prevention and treatment;3Low public recognition of VCI had serious impacts on the effective prevention and treatment of VCI from multiple aspects. Based on the above situation, we proposed corresponding prevention strategies and established prevention and treatment path for VCI.
     Countermeasures:
     1. Strengthen the propaganda, raise public awareness.
     2. Establish nursing training institutions for VCI patients, to eliminate the negative emotions and concerns of caregivers in the care of VCI patients.
     3. Improve medical standards of primary health care workers, standardized general practitioner training, and indeed the implementation of two-way referral system.
     4. Strengthen the VCI professional and technical personnel training, to promote the VCI-related basic research.
     5. Establishment information monitoring system of VCI and the health file of residents.
     6. Suggest the government to increase support for efforts and to increase the investment in prevention and control work for VCI.
     7. Establish prevention path for VCI.
引文
[1]吴兆苏,姚崇华,赵冬,等.我国多省市心血管病趋势及决定因素的人群监测(中国MONICA方案)I.发病率和死亡率监测结果[J].中华心血管病杂志,1997(01).
    [2]Jin Y P, Di Legge S, Ostbye T, et al. The reciprocal risks of stroke and cognitive impairment in an elderly population[J]. Alzheimers Dement, 2006,2(3):171-178.
    [3]Barba R, Martinez-Espinosa S, Rodriguez-Garcia E, et al. Poststroke dementia:clinical features and risk factors[J]. Stroke,2000,31(7):1494-1501.
    [4]Nagai M, Kario K. Chronic kidney disease,24-h blood pressure burden and their effects on silent cerebral injury and cognitive impairment:might age serve as a modulator?[J]. Hypertens Res,2011.
    [5]Germain S, Adam S, Olivier C, et al. Does cognitive impairment influence burden in caregivers of patients with Alzheimer's disease?[J]. J Alzheimers Dis, 2009,17(1):105-114.
    [6]Blake H, Lincoln N B. Cognitive impairments following a stroke:the strain on caregivers [J]. International Journal of Therapy and Rehabilitation, 2002,9(9):334-337.
    [7]中华人民共和国卫生部.2004年中国卫生统计年鉴[M].北京:中国协和医科大学出版社,2004.
    [8]Roman G C. Vascular dementia revisited:diagnosis, pathogenesis, treatment, and prevention[J]. Med Clin North Am,2002,86(3):477-499.
    [9]Hachinski V C, Bowler J V. Vascular dementia[J]. Neurology, 1993,43(10):2159-2160,2160-2161.
    [10]Hachinski V, Iadecola C, Petersen R C, et al. National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards[J]. Stroke,2006,37(9):2220-2241.
    [11]Rockwood K, Black S E, Song X, et al. Clinical and radiographic subtypes of vascular cognitive impairment in a clinic-based cohort study[J]. J Neurol Sci, 2006,240(1-2):7-14.
    [12]Moorhouse P, Rockwood K. Vascular cognitive impairment:current concepts and clinical developments[J]. Lancet Neurol,2008,7(3):246-255.
    [13]van Straaten E C, Scheltens P, Barkhof F. MRI and CT in the diagnosis of vascular dementia[J]. J Neurol Sci,2004,226(1-2):9-12.
    [14]Erkinjuntti T, Inzitari D, Pantoni L, et al. Research criteria for subcortical vascular dementia in clinical trials[J]. J Neural Transm Suppl,2000,59:23-30.
    [15]Merino J G. Dementia after stroke:high incidence and intriguing associations[J]. Stroke,2002,33(9):2261-2262.
    [16]Censori B, Manara O, Agostinis C, et al. Dementia after first stroke[J]. Stroke,1996,27(7):1205-1210.
    [17]Rasquin S M, Verhey F R, van Oostenbrugge R J, et al. Demographic and CT scan features related to cognitive impairment in the first year after stroke[J]. J Neurol Neurosurg Psychiatry,2004,75(11):1562-1567.
    [18]Pohjasvaara T, Erkinjuntti T, Ylikoski R, et al. Clinical determinants of poststroke dementia[J]. Stroke,1998,29(1):75-81.
    [19]Wentzel C, Rockwood K, MacKnight C, et al. Progression of impairment in patients with vascular cognitive impairment without dementia[J]. Neurology, 2001,57(4):714-716.
    [20]Tatemichi T K, Desmond D W, Mayeux R, et al. Dementia after stroke: baseline frequency, risks, and clinical features in a hospitalized cohort[J]. Neurology,1992,42(6):1185-1193.
    [21]Kase C S, Wolf P A, Kelly-Hayes M, et al. Intellectual decline after stroke: the Framingham Study[J]. Stroke,1998,29(4):805-812.
    [22]Tham W, Auchus A P, Thong M, et al. Progression of cognitive impairment after stroke:one year results from a longitudinal study of Singaporean stroke patients[J]. J Neurol Sci,2002,203-204:49-52.
    [23]Han M K, Huh Y, Lee S B, et al. Prevalence of stroke and transient ischemic attack in Korean elders:findings from the Korean Longitudinal Study on Health and Aging (KLoSHA)[J]. Stroke,2009,40(3):966-969.
    [24]刘宏军,方向华,秦晓明,等.北京市社区缺血性卒中患者认知功能障碍及危险因素调查[J].中国脑血管病杂志,2009,6(10):5.
    [25]闫芳,李淑然,黄悦勤,等.北京市城市某社区近20年老年期痴呆患病率纵向比较[J].中国心理卫生杂志,2008,22(2):4.
    [26]郑秀霞,Xiu-xia ZHENG.北京市门头沟区老年期痴呆流行病学调查[J].神经疾病与精神卫生,2010,10(2).
    [27]王红艳,张迎泉,陈宪锐,等.泰安市老年人痴呆患病情况调查[J].中国公共卫生,2009,25(8):2.
    [28]张新庆,丁洪新,郭竹芝,等.山东沿海十县市脑血管性痴呆流行病学调查[J].解放军保健医学杂志,2000,2(4):2.
    [29]范俭雄,言镜玲,陈震华,等.南京地区老年期痴呆流行病学调查[J].临床精神医学杂志,2000,10(3):2.
    [30]徐群,林岩,耿介立,等.缺血性卒中后认知功能障碍的患病率和危险因素[J].中华内科杂志,2008,47(12):4.
    [31]李敬诚,周华东,邓娟,等.首次发作脑梗死患者认知障碍发生率:434例分析(英文)[J].中国临床康复,2005(29).
    [32]邹开利,漆静,何源,等.重庆渝中区街道老年期痴呆横断面研究[J].中华老年医学杂志,2002,21(6):3.
    [33]袁也丰,万爱兰,陈建云,等.南昌市区老年期痴呆的现况调查[J].中华神经医学杂志,2005,4(1):3.
    [34]梁柳娟,林启明,黄朝,等.社区老年人痴呆流行病学调查[J].现代预防医学,2003,30(4):2.
    [35]吴传东,黄进弟,陈维雄,等.海南省城镇Alzheimer氏病和脑血管性痴呆流行病学调查[J].中国热带医学,2003,3(5):2.
    [36]屈秋民,乔晋,杨剑波,等.西安地区中老年人的痴呆患病率调查[J].中华老年医学杂志,2001,20(4):4.
    [37]屈秋民,乔晋,韩建峰,等.陕西省西安地区中老年人痴呆及其主要亚型发病率调查[J].中华流行病学杂志,2005,26(7):4.
    [38]周晓辉,张小宁,郝晨光,等.新疆地区维吾尔族和汉族50岁以上人群脑卒中及血管性痴呆流行病学调查[J].中华流行病学杂志,2008,29(10):2.
    [39]杨期东,周艳宏,谭兴林,等.脑卒中高发区社区人群老年期痴呆的流行病学研究[J].中国临床康复,2002,6(1):2.
    [40]Tang W K, Chan S S, Chiu H F, et al. Frequency and clinical determinants of poststroke cognitive impairment in nondemented stroke patients[J]. J Geriatr Psychiatry Neurol,2006,19(2):65-71.
    [41]Madureira S, Guerreiro M, Ferro J M. Dementia and cognitive impairment three months after stroke[J]. Eur J Neurol,2001,8(6):621-627.
    [42]王永亭,曾丽莉,吕海燕,等.缺血性卒中病因学与发病机制研究的十年进展[J].中国现代神经疾病杂志,2010,10(1):2-27.
    [43]Voltz R, Rosen F V, Yousry T, et al. Reversible encephalopathy with cerebral vasospasm in a Guillain-Barre syndrome patient treated with intravenous immunoglobulin[J]. Neurology,1996,46(1):250-251.
    [44]血管性认知功能损害专家共识组.血管性认知功能损害的专家共识[J].中华内科杂志,2007,46(12):1052-1055.
    [45]Brott T, Adams H J, Olinger C P, et al. Measurements of acute cerebral infarction:a clinical examination scale[J]. Stroke,1989,20(7):864-870.
    [46]Folstein M F, Folstein S E, McHugh P R. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician[J]. J Psychiatr Res,1975,12(3):189-198.
    [47]Nasreddine Z S, Phillips N A, Bedirian V, et al. The Montreal Cognitive Assessment, MoCA:a brief screening tool for mild cognitive impairment[J]. J Am Geriatr Soc,2005,53(4):695-699.
    [48]Lautenschlager N T, Riemenschneider M, Drzezga A, et al. Primary degenerative mild cognitive impairment:study population, clinical, brain imaging and biochemical findings[J]. Dement Geriatr Cogn Disord,2001,12(6):379-386.
    [49]Ehreke L, Luppa M, Konig H H, et al. Is the Clock Drawing Test a screening tool for the diagnosis of mild cognitive impairment? A systematic review[J]. Int Psychogeriatr,2010,22(1):56-63.
    [50]Mitchell A J. A meta-analysis of the accuracy of the mini-mental state examination in the detection of dementia and mild cognitive impairment[J]. J Psychiatr Res,2009,43(4):411-431.
    [51]张明园.精神科评定量表手册[M].长沙:湖南科学技术出版社,1993.
    [52]王延平,徐桂兰,杨少青,等.蒙特利尔认知评估量表识别首次卒中后轻度血管性认知障碍的作用[J].中华神经医学杂志,2010,9(5):503-507.
    [53]Dubois B, Slachevsky A, Litvan I, et al. The FAB:a Frontal Assessment Battery at bedside[J]. Neurology,2000,55(11):1621-1626.
    [54]Oguro H, Yamaguchi S, Abe S, et al.{Differentiating Alzheimer's disease from subcortical vascular dementia with the FAB test}[J].{JOURNAL OF NEUROLOGY}, 2006,{253}({11}):1490-1494.
    [55]Lawton M P, Brody E M. Assessment of older people:self-maintaining and instrumental activities of daily living[J]. Gerontologist,1969,9(3):179-186.
    [56]Reijneveld S A, Spijker J, Dijkshoorn H. Katz'ADL index assessed functional performance of Turkish, Moroccan, and Dutch elderly[J]. J Clin Epidemiol,2007,60(4):382-388.
    [57]Pfeffer R I, Kurosaki T T, Harrah C J, et al. Measurement of functional activities in older adults in the community[J]. J Gerontol,1982,37(3):323-329.
    [58]Lyness J M, Noel T K, Cox C, et al. Screening for depression in elderly primary care patients. A comparison of the Center for Epidemiologic Studies-Depression Scale and the Geriatric Depression Scale[J]. Arch Intern Med, 1997,157(4):449-454.
    [59]肖水源.《社会支持评定量表》的理论基础与研究应用[J].临床精神医学杂志,1994(2):98-100.
    [60]Fazekas F, Chawluk J B, Alavi A, et al. MR signal abnormalities at 1.5 T in Alzheimer's dementia and normal aging[J]. AJR Am J Roentgenol, 1987,149(2):351-356.
    [61]彭丹涛,许贤豪,刘江红,等.简易智能精神状态检查量表检测老年期痴呆患者的应用探讨[J].中国神经免疫学和神经病学杂志,2005(4):187-190.
    [62]杨百瑜.中国12城市45岁以上居民首发卒中后认知损害调查[D].北京协和医学院北京协和医学院;清华大学医学部;中国医学科学院临床医学,2009.
    [63]Sachdev P S, Brodaty H, Valenzuela M J, et al. Clinical determinants of dementia and mild cognitive impairment following ischaemic stroke:the Sydney Stroke Study[J]. Dement Geriatr Cogn Disord,2006,21 (5-6):275-283.
    [64]Inzitari D, Di Carlo A, Pracucci G, et al. Incidence and determinants of poststroke dementia as defined by an informant interview method in a hospital-based stroke registry[J]. Stroke,1998,29(10):2087-2093.
    [65]Kokmen E, Whisnant J P, O'Fallon W M, et al. Dementia after ischemic stroke:a population-based study in Rochester, Minnesota (1960-1984)[J]. Neurology,1996,46(1):154-159.
    [66]Zhou D H, Wang J Y, Li J, et al. Frequency and risk factors of vascular cognitive impairment three months after ischemic stroke in china:the Chongqing stroke study[J]. Neuroepidemiology,2005,24(1-2):87-95.
    [67]Hebert R, Lindsay J, Verreault R, et al. Vascular dementia:incidence and risk factors in the Canadian study of health and aging[J]. Stroke, 2000,31(7):1487-1493.
    [68]任艳丁,王淑荣.老年腔隙性脑梗死血管性认知障碍与病灶部位关系[J].中国血液流变学杂志,2009,19(2):220-221.
    [69]白伟利,屈宝华.头颅CT所见脑萎缩与年龄关系的相关分析[J].中国实用神经疾病杂志,2008,11(10):18-19.
    [70]Goldbourt U, Schnaider-Beeri M, Davidson M. Socioeconomic status in relationship to death of vascular disease and late-life dementia[J]. J Neurol Sci, 2007,257(1-2):177-181.
    [71]贾建平,王荫华,丁新生,等.中国痴呆与认知障碍诊断指南[M].人民卫生出版社,2010.
    [72]van Exel E, Gussekloo J, de Craen A J, et al. Cognitive function in the oldest old:women perform better than men[J]. J Neurol Neurosurg Psychiatry, 2001,71(1):29-32.
    [73]Kauhanen M, Korpelainen J T, Hiltunen P, et al. Poststroke depression correlates with cognitive impairment and neurological deficits[J]. Stroke, 1999,30(9):1875-1880.
    [74]Talelli P, Ellul J, Terzis G, et al. Common carotid artery intima media thickness and post-stroke cognitive impairment[J]. J Neurol Sci, 2004,223(2):129-134.
    [75]Sachdev P S, Brodaty H, Valenzuela M J, et al. Progression of cognitive impairment in stroke patients[J]. Neurology,2004,63(9):1618-1623.
    [76]张振馨.认知功能障碍研究进展[J].中华内科杂志,2005(8):633-634.
    [77]刘仙芸,韩布新.认知损伤对老年人生活质量影响的研究进展[J].中国老年学杂志,2004(11):1083-1084.
    [78]Aprile I, Di Stasio E, Romitelli F, et al. Effects of rehabilitation on quality of life in patients with chronic stroke[J]. Brain Inj,2008,22(6):451-456.
    [79]Fong K N, Chan C C, Au D K. Relationship of motor and cognitive abilities to functional performance in stroke rehabilitation[J]. Brain Inj, 2001,15(5):443-453.
    [80]McDonald R J, Craig L A, Hong N S. Enhanced cell death in hippocampus and emergence of cognitive impairments following a localized mini-stroke in hippocampus if preceded by a previous episode of acute stress [J]. Eur J Neurosci, 2008,27(8):2197-2209.
    [81]Doyle P J. Measuring health outcomes in stroke survivors[J]. Arch Phys Med Rehabil,2002,83(12 Suppl 2):S39-S43.
    [82]Klages J D, Fisk J D, Rockwood K. APOE genotype, vascular risk factors, memory test performance and the five-year risk of vascular cognitive impairment or Alzheimer's disease[J]. Dement Geriatr Cogn Disord,2005,20(5):292-297.
    [83]MacKnight C, Rockwood K, Awalt E, et al. Diabetes mellitus and the risk of dementia, Alzheimer's disease and vascular cognitive impairment in the Canadian Study of Health and Aging[J]. Dement Geriatr Cogn Disord,2002,14(2):77-83.
    [84]Maxwell C J, Hogan D B, Ebly E M. Serum folate levels and subsequent adverse cerebrovascular outcomes in elderly persons[J]. Dement Geriatr Cogn Disord,2002,13(4):225-234.
    [85]Rockwood K, Ebly E, Hachinski V, et al. Presence and treatment of vascular risk factors in patients with vascular cognitive impairment[J]. Arch Neurol, 1997,54(1):33-39.
    [86]Sacco R L. Newer risk factors for stroke[J]. Neurology,2001,57(5 Suppl 2):S31-S34.
    [87]Boden-Albala B, Cammack S, Chong J, et al. Diabetes, fasting glucose levels, and risk of ischemic stroke and vascular events:findings from the Northern Manhattan Study (NOMAS)[J]. Diabetes Care,2008,31(6):1132-1137.
    [88]Boden-Albala B, Sacco R L, Lee H S, et al. Metabolic syndrome and ischemic stroke risk:Northern Manhattan Study[J]. Stroke,2008,39(1):30-35.
    [89]Khatri M, Wright C B, Nickolas T L, et al. Chronic kidney disease is associated with white matter hyperintensity volume:the Northern Manhattan Study (NOMAS)[J]. Stroke,2007,38(12):3121-3126.
    [90]Boden-Albala B, Elkind M S, White H, et al. Dietary total fat intake and ischemic stroke risk:the Northern Manhattan Study[J]. Neuroepidemiology, 2009,32(4):296-301.
    [91]Suk S H, Sacco R L, Boden-Albala B, et al. Abdominal obesity and risk of ischemic stroke:the Northern Manhattan Stroke Study[J]. Stroke, 2003,34(7):1586-1592.
    [92]Boden-Albala B, Litwak E, Elkind M S, et al. Social isolation and outcomes post stroke[J]. Neurology,2005,64(11):1888-1892.
    [93]Elkind M S, Cheng J, Rundek T, et al. Leukocyte count predicts outcome after ischemic stroke:the Northern Manhattan Stroke Study[J]. J Stroke Cerebrovasc Dis,2004,13(5):220-227.
    [94]Elkind M S, Sciacca R, Boden-Albala B, et al. Moderate alcohol consumption reduces risk of ischemic stroke:the Northern Manhattan Study[J]. Stroke,2006,37(1):13-19.
    [95]Willey J Z, Moon Y P, Paik M C, et al. Physical activity and risk of ischemic stroke in the Northern Manhattan Study[J]. Neurology,2009,73(21):1774-1779.
    [96]Elkind M S, Flint A C, Sciacca R R, et al. Lipid-lowering agent use at ischemic stroke onset is associated with decreased mortality[J]. Neurology, 2005,65(2):253-258.
    [97]Manly J J, Jacobs D M, Sano M, et al. Effect of literacy on neuropsychological test performance in nondemented, education-matched elders[J]. J Int Neuropsychol Soc,1999,5(3):191-202.
    [98]徐群,林岩,耿介立,等.皮质下缺血性脑血管病的临床特点和危险因素[J].中国卒中杂志,2007(6):468-471.
    [99]胡昔权,兰月,郑海清,等.初发脑卒中后认知功能障碍的相关因素分析[J].中华医学杂志,2009,89(41):4.
    [100]师景英.脑梗死后血管性认知障碍的危险因素分析[J].中西医结合心脑血管病杂志,2008(8).
    [101]王利平,卜淑霞,包晓群,等.脑梗死后血管性认知障碍影响因素的探讨[J].中国老年学杂志,2007(7).
    [102]Doyle P J. Measuring health outcomes in stroke survivors[J]. Arch Phys Med Rehabil,2002,83(12 Suppl 2):S39-S43.
    [103]胡晓抒,郭志荣,周慧,等.江苏省35~74岁人群代谢综合征的流行病学调查[J].中华流行病学杂志,2006,27(9):751-756.
    [104]Patel M D, Coshall C, Rudd A G, et al. Cognitive impairment after stroke: clinical determinants and its associations with long-term stroke outcomes[J]. J Am Geriatr Soc,2002,50(4):700-706.
    [105]Talelli P, Ellul J, Terzis G, et al. Common carotid artery intima media thickness and post-stroke cognitive impairment[J]. J Neurol Sci, 2004,223(2):129-134.
    [106]Newman G C, Bang H, Hussain S I, et al. Association of diabetes, homocysteine, and HDL with cognition and disability after stroke[J]. Neurology, 2007,69(22):2054-2062.
    [107]Yip A G, Brayne C, Matthews F E. Risk factors for incident dementia in England and Wales:The Medical Research Council Cognitive Function and Ageing Study. A population-based nested case-control study[J]. Age Ageing, 2006,35(2):154-160.
    [108]Lopez O L, Kuller L H, Becker J T. Diagnosis, risk factors, and treatment of vascular dementia[J]. Curr Neurol Neurosci Rep,2004,4(5):358-367.
    [109]Andel R, Crowe M, Hahn E A, et al. Work-related stress may increase the risk of vascular dementia[J]. J Am Geriatr Soc,2012,60(1):60-67.
    [110]Desmond D W, Moroney J T, Paik M C, et al. Frequency and clinical determinants of dementia after ischemic stroke[J]. Neurology, 2000,54(5):1124-1131.
    [111]de Magalhaes J P, Sandberg A. Cognitive aging as an extension of brain development:a model linking learning, brain plasticity, and neurodegeneration[J]. Mech Ageing Dev,2005,126(10):1026-1033.
    [112]Wight R G, Aneshensel C S, Seeman T E. Educational attainment, continued learning experience, and cognitive function among older men[J]. J Aging Health, 2002,14(2):211-236.
    [113]王本孝,黄自丽,许平.血管性认知功能障碍的临床研究进展[J].神经损伤与功能重建,2009(4):291-293.
    [114]Tang W K, Chan S S, Chiu H F, et al. Frequency and determinants of poststroke dementia in Chinese[J]. Stroke,2004,35(4):930-935.
    [115]Forette F, Seux M L, Staessen J A, et al. The prevention of dementia with antihypertensive treatment:new evidence from the Systolic Hypertension in Europe (Syst-Eur) study[J]. Arch Intern Med,2002,162(18):2046-2052.
    [116]Petrovitch H, White L R, Izmirilian G, et al. Midlife blood pressure and neuritic plaques, neurofibrillary tangles, and brain weight at death:the HAAS. Honolulu-Asia aging Study[J]. Neurobiol Aging,2000,21(1):57-62.
    [117]Posner H B, Tang M X, Luchsinger J, et al. The relationship of hypertension in the elderly to AD, vascular dementia, and cognitive function[J]. Neurology, 2002,58(8):1175-1181.
    [118]In'T V B, Ruitenberg A, Hofinan A, et al. Antihypertensive drugs and incidence of dementia:the Rotterdam Study[J]. Neurobiol Aging, 2001,22(3):407-412.
    [119]Xu W L, Qiu C X, Wahlin A, et al. Diabetes mellitus and risk of dementia in the Kungsholmen project:a 6-year follow-up study [J]. Neurology, 2004,63(7):1181-1186.
    [120]Hassing L B, Johansson B, Nilsson S E, et al. Diabetes mellitus is a risk factor for vascular dementia, but not for Alzheimer's disease:a population-based study of the oldest old[J]. Int Psychogeriatr,2002,14(3):239-248.
    [121]Allen K V, Frier B M, Strachan M W. The relationship between type 2 diabetes and cognitive dysfunction:longitudinal studies and their methodological limitations[J]. Eur J Pharmacol,2004,490(1-3):169-175.
    [122]Kilander L, Andren B, Nyman H, et al. Atrial fibrillation is an independent determinant of low cognitive function:a cross-sectional study in elderly men[J]. Stroke,1998,29(9):1816-1820.
    [123]Reitz C, Luchsinger J, Tang M X, et al. Effect of smoking and time on cognitive function in the elderly without dementia[J]. Neurology, 2005,65(6):870-875.
    [124]Suryadevara V, Storey S G, Aronow W S, et al. Association of abnormal serum lipids in elderly persons with atherosclerotic vascular disease and dementia, atherosclerotic vascular disease without dementia, dementia without atherosclerotic vascular disease, and no dementia or atherosclerotic vascular disease[J]. J Gerontol A Biol Sci Med Sci,2003,58(9):M859-M861.
    [125]Moroney J T, Bagiella E, Desmond D W, et al. Risk factors for incident dementia after stroke. Role of hypoxic and ischemic disorders [J]. Stroke, 1996,27(8):1283-1289.
    [126]Rastas S, Verkkoniemi A, Polvikoski T, et al. Atrial fibrillation, stroke, and cognition:a longitudinal population-based study of people aged 85 and older[J]. Stroke,2007,38(5):1454-1460.
    [127]Grubb N R. Managing out-of-hospital cardiac arrest survivors:1. Neurological perspective[J]. Heart,2001,85(1):6-8.
    [128]Rao R, Jackson S, Howard R. Neuropsychological impairment in stroke, carotid stenosis, and peripheral vascular disease, A comparison with healthy community residents [J]. Stroke,1999,30(10):2167-2173.
    [129]于荣焕,裘丽红,何蕴,等.短暂性脑缺血发作与血管性认知功能障碍的临床研究[J].中国老年学杂志,2008(24).
    [130]罗鸣,罗卓荆,师晓宸,等.椎动脉型颈椎病患者的记忆障碍特征调查[J].中国临床康复,2005(12).
    [131]张强,张其梅,李耀彩,等.颈动脉狭窄与认知功能障碍研究进展[J].神经疾病与精神卫生,2009,9(1):2.
    [132]段炜,陈康宁,柳春雨,等.解除颈动脉狭窄治疗轻度认知功能障碍的实验研究[J].国际脑血管病杂志,2006,14(6):5.
    [133]Gorelick P B, Freels S, Harris Y, et al. Epidemiology of vascular and Alzheimer's dementia among African Americans in Chicago, IL:baseline frequency and comparison of risk factors[J]. Neurology,1994,44(8):1391-1396.
    [134]Mackowiak-Cordoliani M A, Bombois S, Memin A, et al. Poststroke dementia in the elderly[J]. Drugs Aging,2005,22(6):483-493.
    [135]Bowler J V. The concept of vascular cognitive impairment[J]. J Neurol Sci, 2002,203-204:11-15.
    [136]Stampfer M J, Kang J H, Chen J, et al. Effects of moderate alcohol consumption on cognitive function in women[J]. N Engl J Med, 2005,352(3):245-253.
    [137]Hong J T, Ryu S R, Kim H J, et al. Neuroprotective effect of green tea extract in experimental ischemia-reperfusion brain injury[J]. Brain Res Bull, 2000,53(6):743-749.
    [138]van Exel E, Gussekloo J, Houx P, et al. Atherosclerosis and cognitive impairment are linked in the elderly. The Leiden 85-plus Study[J]. Atherosclerosis,2002,165(2):353-359.
    [139]Negishi H, Xu J W, Ikeda K, et al. Black and green tea polyphenols attenuate blood pressure increases in stroke-prone spontaneously hypertensive rats[J]. J Nutr,2004,134(1):38-42.
    [140]聂曦,陈智,李鸿元.高血压并发脑卒中危险因素的调查[J].局解手术学杂志,2009,18(3):180.
    [141]吴振云,许淑莲,孙长华,等.高龄老人的认知功能和心理健康[J].中国人口科学,2001:59-62.
    [142]Tuokko H, Frerichs R, Graham J, et al. Five-year follow-up of cognitive impairment with no dementia[J]. Arch Neurol,2003,60(4):577-582.
    [143]方文莉,郑宏,张敏敏,等.痴呆知晓率与态度的社区调查[J].老年医学与保健,2010,16(4):237-240,244.
    [144]王岚,王学义,许顺江,等.石家庄市普通民众对老年期痴呆的知晓率调查[J].中国健康心理学杂志,2012(3):355-357.
    [145]张振馨,陈霞,刘协和,等.北京、西安、上海、成都四地区痴呆患者卫生保健现状调查[J].中国医学科学院学报,2004,26(2):116-121.
    [146]顾美铮,王国宝.2047名老年人群及其照料者心理保健知识知晓率调查[J].上海精神医学,2005,17(z1):14-15.
    [147]山媛,屈秋民,郭峰,等.门诊痴呆患者诊断率低的原因分析[J].中华老年医学杂志,2011,30(10):820-822.
    [148]王乐三.SPSS在医学科研中的应用[M].第1版(2007年8月1日),2007.
    [149]Schwalen S, Forstl H. [Alzheimer's disease:knowledge and attitudes in a representative survey][J]. Neuropsychiatr,2008,22(1):35-37.
    [150]张振馨,陈霞,刘协和,等.北京、西安、上海、成都四地区痴呆患者卫生保健现状调查[J].中国医学科学院学报,2004,26(2):116-121.
    [151]Srikanth V K, Thrift A G, Saling M M, et al. Increased risk of cognitive impairment 3 months after mild to moderate first-ever stroke:a Community-Based Prospective Study of Nonaphasic English-Speaking Survivors[J]. Stroke,2003,34(5):1136-1143.
    [152]Tatemichi T K, Desmond D W, Stern Y, et al. Cognitive impairment after stroke:frequency, patterns, and relationship to functional abilities[J]. J Neurol Neurosurg Psychiatry,1994,57(2):202-207.
    [153]Mori E. Impact of subcortical ischemic lesions on behavior and cognition[J]. Ann N Y Acad Sci,2002,977:141-148.
    [154]Sarti C, Pantoni L, Bartolini L, et al. Cognitive impairment and chronic cerebral hypoperfusion:what can be learned from experimental models[J]. J Neurol Sci,2002,203-204:263-266.
    [155]Zhu L, Fratiglioni L, Guo Z, et al. Association of stroke with dementia, cognitive impairment, and functional disability in the very old:a population-based study[J]. Stroke,1998,29(10):2094-2099.
    [1]Erkinjuntti T, Gauthier S. The concept of vascular cognitive impairment[J]. Front Neurol Neurosci,2009,24:79-85.
    [2]Nyenhuis, L D. VASCULAR COGNITIVE IMPAIRMENT:A COMMON SEQUELAE OF STROKE AND ITS PREVENTION. CONTINUUM:Lifelong Learning in Neurology[Z].2005:11,137-153.
    [3]Hachinski V, Iadecola C, Petersen R C, et al. National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards[J]. Stroke,2006,37(9):2220-2241.
    [4]Pohjasvaara T, Erkinjuntti T, Vataja R, et al. Dementia three months after stroke. Baseline frequency and effect of different definitions of dementia in the Helsinki Stroke Aging Memory Study (SAM) cohort[J]. Stroke,1997,28(4):785-792.
    [5]Tatemichi T K, Desmond D W, Mayeux R, et al. Dementia after stroke:baseline frequency, risks, and clinical features in a hospitalized cohort[J]. Neurology, 1992,42(6):1185-1193.
    [6]Tatemichi T K, Paik M, Bagiella E, et al. Risk of dementia after stroke in a hospitalized cohort:results of a longitudinal study[J]. Neurology, 1994,44(10):1885-1891.
    [7]Sachdev P S, Brodaty H, Valenzuela M J, et al. Progression of cognitive impairment in stroke patients[J]. Neurology,2004,63(9):1618-1623.
    [8]Tatemichi T K, Foulkes M A, Mohr J P, et al. Dementia in stroke survivors in the Stroke Data Bank cohort. Prevalence, incidence, risk factors, and computed tomographic findings[J]. Stroke,1990,21(6):858-866.
    [9]Kokmen E, Whisnant J P, O'Fallon W M, et al. Dementia after ischemic stroke:a population-based study in Rochester, Minnesota (1960-1984)[J]. Neurology, 1996,46(1):154-159.
    [10]Tang W K, Chan S S, Chiu H F, et al. Frequency and clinical determinants of poststroke cognitive impairment in nondemented stroke patients[J]. J Geriatr Psychiatry Neurol,2006,19(2):65-71.
    [11]Rasquin S M, Lodder J, Verhey F R. Predictors of reversible mild cognitive impairment after stroke:a 2-year follow-up study[J]. J Neurol Sci, 2005,229-230:21-25.
    [12]Inzitari D, Di Carlo A, Pracucci G, et al. Incidence and determinants of poststroke dementia as defined by an informant interview method in a hospital-based stroke registry[J]. Stroke,1998,29(10):2087-2093.
    [13]Desmond D W, Moroney J T, Paik M C, et al. Frequency and clinical determinants of dementia after ischemic stroke[J]. Neurology, 2000,54(5):1124-1131.
    [14]Pohjasvaara T, Erkinjuntti T, Ylikoski R, et al. Clinical determinants of poststroke dementia[J]. Stroke,1998,29(1):75-81.
    [15]Zhou D H, Wang J Y, Li J, et al. Frequency and risk factors of vascular cognitive impairment three months after ischemic stroke in china:the Chongqing stroke study[J]. Neuroepidemiology,2005,24(1-2):87-95.
    [16]Wright C B, Elkind M S, Rundek T, et al. Alcohol intake, carotid plaque, and cognition:the Northern Manhattan Study[J]. Stroke,2006,37(5):1160-1164.
    [17]Del S T, Barba R, Morin M M, et al. Evolution of cognitive impairment after stroke and risk factors for delayed progression[J]. Stroke, 2005,36(12):2670-2675.
    [18]Roman G C. Brain hypoperfusion:a critical factor in vascular dementia[J]. Neurol Res,2004,26(5):454-458.
    [19]Manolio T A, Olson J, Longstreth W T. Hypertension and cognitive function: pathophysiologic effects of hypertension on the brain[J]. Curr Hypertens Rep, 2003,5(3):255-261.
    [20]Rowan E, Morris C M, Stephens S, et al. Impact of hypertension and apolipoprotein E4 on poststroke cognition in subjects>75 years of age[J]. Stroke,2005,36(9):1864-1868.
    [21]Henon H, Durieu I, Guerouaou D, et al. Poststroke dementia:incidence and relationship to prestroke cognitive decline[J]. Neurology,2001,57(7):1216-1222.
    [22]Vermeer S E, Prins N D, den Heijer T, et al. Silent brain infarcts and the risk of dementia and cognitive decline[J]. N Engl J Med,2003,348(13):1215-1222.
    [23]Desmond D W, Moroney J T, Sano M, et al. Recovery of cognitive function after stroke[J]. Stroke,1996,27(10):1798-1803.
    [24]Barba R, Martinez-Espinosa S, Rodriguez-Garcia E, et al. Poststroke dementia: clinical features and risk factors[J]. Stroke,2000,31 (7):1494-1501.
    [25]Sachdev P. Homocysteine, cerebrovascular disease and brain atrophy[J]. J Neurol Sci,2004,226(1-2):25-29.
    [26]Rowan E N, Dickinson H O, Stephens S, et al. Homocysteine and post-stroke cognitive decline[J]. Age Ageing,2007,36(3):339-343.
    [27]Censori B, Manara O, Agostinis C, et al. Dementia after first stroke[J]. Stroke, 1996,27(7):1205-1210.
    [28]Gamaldo A, Moghekar A, Kilada S, et al. Effect of a clinical stroke on the risk of dementia in a prospective cohort[J]. Neurology,2006,67(8):1363-1369.
    [29]Srikanth V K, Quinn S J, Donnan G A, et al. Long-term cognitive transitions, rates of cognitive change, and predictors of incident dementia in a population-based first-ever stroke cohort[J]. Stroke,2006,37(10):2479-2483.
    [30]Mok V C, Wong A, Lam W W, et al. Cognitive impairment and functional outcome after stroke associated with small vessel disease[J]. J Neurol Neurosurg Psychiatry,2004,75(4):560-566.
    [31]Srikanth V K, Thrift A G, Saling M M, et al. Increased risk of cognitive impairment 3 months after mild to moderate first-ever stroke:a Community-Based Prospective Study of Nonaphasic English-Speaking Survivors[J]. Stroke,2003,34(5):1136-1143.
    [32]Tang W K, Chan S S, Chiu H F, et al. Frequency and determinants of poststroke dementia in Chinese[J]. Stroke,2004,35(4):930-935.
    [33]Pohjasvaara T, Mantyla R, Salonen O, et al. How complex interactions of ischemic brain infarcts, white matter lesions, and atrophy relate to poststroke dementia[J]. Arch Neurol,2000,57(9):1295-1300.
    [34]Sachdev P S, Brodaty H, Valenzuela M J, et al. Clinical determinants of dementia and mild cognitive impairment following ischaemic stroke:the Sydney Stroke Study[J]. Dement Geriatr Cogn Disord,2006,21 (5-6):275-283.
    [35]Tatemichi T K, Desmond D W, Stern Y, et al. Cognitive impairment after stroke: frequency, patterns, and relationship to functional abilities[J]. J Neurol Neurosurg Psychiatry,1994,57(2):202-207.
    [36]Kauhanen M, Korpelainen J T, Hiltunen P, et al. Poststroke depression correlates with cognitive impairment and neurological deficits[J]. Stroke, 1999,30(9):1875-1880.
    [37]Kimura M, Robinson R G, Kosier J T. Treatment of cognitive impairment after poststroke depression:a double-blind treatment trial[J]. Stroke, 2000,31(7):1482-1486.
    [38]Rastas S, Verkkoniemi A, Polvikoski T, et al. Atrial fibrillation, stroke, and cognition:a longitudinal population-based study of people aged 85 and older[J]. Stroke,2007,38(5):1454-1460.
    [39]Zhu L F L G Z. Incidence of dementia in relation to stroke and the apolipoprotein E epsilon 4 allele in the very old. Findings from a population-based longitudinal study[Z].200053-60.
    [40]Klimkowicz A, Slowik A, Dziedzic T, et al. Post-stroke dementia is associated with alpha(1)-antichymotrypsin polymorphism[J]. J Neurol Sci, 2005,234(1-2):31-36.
    [41]Arpa A, Del S T, Goda G, et al. Apolipoprotein E, angiotensin-converting enzyme and alpha-1-antichymotrypsin genotypes are not associated with post-stroke dementia[J]. J Neurol Sci,2003,210(1-2):77-82.
    [42]Morris C M, Ballard C G, Allan L, et al. NOS3 gene rs1799983 polymorphism and incident dementia in elderly stroke survivors [J]. Neurobiol Aging, 2011,32(3):551-554.

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