首次发病的腔隙性脑梗死认知功能变化的研究
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
目的:研究急性腔隙性脑梗死认知功能障碍及其演变。
     方法:在一家三级甲等教学医院前瞻性选取首次发病、病程< 2周的腔隙性脑梗死(lacunar infarction, LI)患者,同时选取正常人作为对照组。发病72 h内分别应用简易智力状态检查量表(mini-mental state examination, MMSE)和蒙特利尔认知评估量表(Montreal Cognitive Assessment, MoCA)进行认知功能评定,并予1个月、3个月、6个月时进行上述神经心理测试的随访。采用SPSS13.0软件包对各项指标进行分析统计,P<0.05为差异有统计学意义。
     结果:1.共纳入LI患者70例,60例正常人作为对照。受试者中基底节16例、丘脑14例、脑干10例、侧脑室旁18例和半卵圆中心12例,其中25例(36%)出现了不同程度的认知功能障碍。
     2. Logistic回归分析显示LI患者认知功能障碍的出现与高血压、糖尿病、高脂血症及高同型半胱氨酸血症(hypercholesterolemia, HHcy)有关(P<0.05)。
     3.与正常对照组比较,基底节、丘脑、脑干、侧脑室旁和半卵圆中心五个部位无论是在MoCA总分,还是视空间技能与执行功能、注意、语言、抽象和延迟回忆因子评分具有显著差异(P<0.05),而计算、命名和定向力无显著差异(P>0.05)。基底节、丘脑、脑干、侧脑室旁和半卵圆中心五个部位之间比较:(1)延迟回忆:丘脑、基底节与其余三个部位比较具有显著差异(P<0.05);(2)语言:丘脑、基底节与其余三个部位比较有显著差异(P<0.05);(3)视空间与执行功能:基底节与其余四个部位比较具有显著差异(P<0.05);(4)注意力:脑干与其余四个部位比较具有显著差异(P<0.05)。
     4.与72 h认知功能相比,LI患者在随访的1个月、3个月和6个月时的注意力评分均明显改善(P<0.05),基本恢复至正常对照组水平。视空间技能与执行功能、语言、延迟回忆评分虽有好转,6个月后仍与正常对照组有明显差异(P<0.05),恢复较差。
     结论:1.首次发病的LI常可出现认知功能障碍,高血压、糖尿病、高脂血症及高同型半胱氨酸血症与认知功能障碍的出现密切相关。
     2.病灶部位是LI患者出现认知功能受损的重要因素,病灶体积与认知功能无明显关系。病变部位多在基底节、丘脑、脑干、侧脑室旁和半卵圆中心,其中,基底节、丘脑对认知功能的影响最大,主要累及视空间技能与执行功能、语言和延迟回忆。
     3. LI发病急性期对认知影响最大,随后认知状况可部分恢复,注意力恢复较好;而视空间与执行、语言和延迟回忆恢复差。6个月后仍可遗留不同程度的认知功能障碍。提示急性LI与认知功能障碍关系密切,值得重视和早期干预。
Objectives: To investigate the characteristics of cognitive impairment on patients with acute first-ever lacunar infarction and its evolution. Methods: In a 3A-level teaching hospital, the cognitive performance was prospectively assessed in patients with acute first-ever lacunar infarction and the normal control. The neuropsychological tests included the mini-mental state examination (MMSE) and the scale of Montreal Cognitive Assessment (MoCA). The relationship between the cognitive impairment and lesion location was analyzed, and the risk factors of cognitive impairment were evaluated. The neuropsychological tests were revaluated at 1st month, 3rd month and 6th month. Statistical analyses were performed with the software package of SPSS13.0, with 2-taile P<0.05 considered statistically efficient. Results: 1. 70 patients with acute first-ever lacunar infarction and 60 normal control were selected in the study. Based on the lesion, there were 16 basal ganglia, 14 thalamus, 10 brainstem, 18 periventricular location, 12 corona radiate in 70 patients. 25 LI patients experienced cognitive impairment (36%).
     2. By logistic regression analysis, the result showed that the onsets of cognitive impairment had correlation with hypertension, diabetes mellitus, hypercholesterolemia and hyperhomocysteinemia (P<0.05).
     3. Compared with control subject, patients with lesion locations in basal ganglia, thalamus, brainstem, periventricular location, corona radiate had significantly lower scores in visual spatial and executive function, attention, language, abstraction and memory factors(P<0.05); but no significant difference in calculation, naming and orientation factors(P>0.05). Comparisons between the five lesion locations:
     (1)patients with lesions in basal ganglia, thalamus had significantly low scores in memory compared with other three lesion locations (P<0.05); (2)patient with lesions in basal ganglia, thalamus had also significantly lower scores in language compared with other three lesion locations (P<0.05);(3) patients with lesions in basal had significantly lower scores in visual spatial and executive function compared with other four lesion locations (P<0.05);(4)The patients with lesions in brainstem performed poorer in attention factor score compared with other four lesion locations (P<0.05).
     4. During the follow-up, there were significantly differences in the scores of attention 1month, 3 month, 6 month after attack compared with 72 hours’, which had reached normal level of the control (P<0.05). Significant differences was found between the control and patients with LI after 6 months in scores of visual spatial and executive function, language, abstraction and memory factors(P<0.05), though it showed a favorable turn. It seemed improved poorly after LI.
     Conclusions: 1. First-ever lacunar infarction usually undergo vascular cognitive impairment. It is closely related to multiple factors, such as hypertension, diabetes mellitus, hypercholesterolemia and hyperhomocysteinemia.
     2. The location of lesion is considered important factor contributing to cognitive impairment, but there is no significant relationship between cognitive dysfunction and ischemic location volume. The ischemic lesions are found in basal ganglia, thalamus, brainstem, periventricular location as well as corona radiate. The location of lesions in basal ganglia, thalamus can lead to cognitive impairments, especially in language, memory, visual spatial and executive function.
     3. LI in acute stage can cause cognitive impairment which improve partly after stoke, with an excellent benign prognosis for recovery in attention but poor in memory, visual spatial and executive function. Patients with LI may undergo varying severity of cognitive impairments for 6 moths after they discharge from hospital. There are mild to severe cognitive dysfunction in the first-ever diagnosed LI patients, which need pay attention to and intervene in time.
引文
[1] Rockwood K. Vascular cognitive impairment and vascular dementia[J].Neurol Sci, 2002, 203-204:23-7.
    [2]贾建平,魏翠柏.血管性认知障碍提出的临床意义[J].中华老年医学杂志,2005,24(1):9-11.
    [3] Hachinski VC, Bowler JV. Vascular dementia [J]. Neurology, 1993, 43(2):250-260.
    [4]杜万良,王荫华.血管性认知障碍[J].中国康复理论与实践,2004,10(4):238-240.
    [5] Bowler JV. Modern concept of Vascular cognitive impairment [J].Br Med Bull, 2007, 83(4): 291-305.
    [6] Moorhouse P,Rockwood K.Vascular cognitive impairment:current concepts and clinical developments[J].Lancet Neurol, 2008, 7(3):246-255.
    [7] Petersen RC, Doody R, Kurz A , et al. Current concepts in mild cognitive impairment [J].Arch Neurol, 2001,58:1985-1992.
    [8]贾建平.重视血管性认知障碍的标准建立和临床研究[J].中国脑血管病杂志,2004,14(1):2-4.
    [9] Rockwood K , Wentzel C, Hachinski V ,et al. Prevalence and out comes of vascular cognitive impairment .Vascular Cognitive Impairment Investigators of the Canadian Study of Health and Aging[J]. Neurology, 2000, 54(2):447-451.
    [10] Tuokko H , Frerichs R ,Graham J, et al. Five-year follow of cognitive impairment with no dementia[J].Arch Neurol, 2003, 60(4):577-582.
    [11]陈湛情,陆兵勋,陈文荣,等.脑梗死后情感障碍和认知障碍的影响因素[J].中国神经精神疾病杂志,2008,34(7):417-421.
    [12] O’Donnell HC , Rosand J, Knudsen KA , et al. Apolipoprotein E genotype and the risk of recurrent lobar intracerebral hemorrhage[J].N Engl J Med, 2000, 342(4): 240-245.
    [13] Carmelli D, Swan GE, Reed T, et al. Midlife cardiovascular risk factors, ApoE and cognitive decline in elderly male twins[J]. Neurology, 1998, 50:1580-1585.
    [14] Madureira S ,Guerreiro M, Ferro JM, et al. Dementia and cognitive impairment three months after stroke[J]. Eur J Neurol, 2001, 8(6):621-627.
    [15] Desmond DW, Moroney JT, Paik MC, et al. Frequency and clinical determinants of dementia after ischemic stroke[J]. Neurology, 2000, 54:1124-1131.
    [16] Pantoni L, Lammine A. Cerebral small vessel disease: Pathological and pathophysiologicalaspects in relation to vascular cognitive impairment. In: Erkinjunti T, Gauthier S, eds [M]. Vascular cognitive impairment, London: Martin Duniz publishers, 2002: 1115-1134.
    [17] Hachinski V, Ladecola C, Petersen RC, et al. National Institute of Neurological Disorders and Stroke-Canadian Stroke Network vascular cognitive impairment harmonization standards[J].Stroke, 2006, 37(9):2220~2241.
    [18] Reed BR, Mungas DM, Kramer JH,et a1. Profiles of Neuropsychological impairment in autopsy-defined Alzheimer’s disease and cerebrovascular disease[J]. Brain, 2007, 130:731~739.
    [19] Sachdev PS, Brodaty H, Valenzuela MJ, et a1. The neuropsychological profile of vascular cognitive impairment in stroke and TIA patients [J]. Neurology, 2004, 62(6): 912-919.
    [20] Ingles JL,Boulton DC,Fisk JD, et a1.Preclinical vascular cognitive impairment and Alzheimer disease: neuropsychological test performance 5 years before diagnosis[J]. Stroke, 2007, 38:1148-1153.
    [21] Muller M, Grobbee DE, Aleman A, et a1.Cardiovascular disease and Cognitive performance in middle-aged and elderly men [J].Atherosclerosis, 2007,190:143-149.
    [22] Haley A P, Sweet L H, Gunstad J, et a1.Verbal working memory and atherosclerosis in patients with cardiovascular disease:an fMRI study [J]. Neuroimaging, 2007, 17:227-233.
    [23] Goessens BM, Visseren FL, Kappelle LJ, et a1.Asymptomatic carotid artery stenosis and the risk of new vascular events in patients with manifest arterial disease[J]. Stroke, 2007, 38(5): 1470-1475.
    [24] Rockwood K, Black S, Kertesz A, et al. Non-cognitive behavioral symptoms in vascular cognitive impairment[J]. Int Psychogeriatr, 2003, 15 (2):50.
    [25] Nasreddine ZS, Phillips NA, Bédirian V, et a1. The Montreal cognitive assessment, MoCA:a brief screening tool for mild cognitive impairment[J]. J Am Geriatr Soc, 2005, 53(4): 695-699.
    [26] Irena MP, Vesna S, Vida D. Mild cognitive impairment in symptomatic and asymptomatic cerebrovascular disease[J].Neurological Science,2007,257(1-2):185-193.
    [27]贾建平.重视血管性障碍的早期诊断和干预[J].中华神经科杂志,2005,38(1):4-5.
    [28]瞿正方.器质性痴呆的CT临床再诊断[J].临床精神医学杂志,1997,7 (1):3-5.
    [29] Rockwood K, Black SE, Song X, et al. Clinical and radiographic subtypes of vascular cognitive impairment in a clinic-based cohort study[J]. J Neurol Sci, 2006,240:7-14.
    [30] Yan zhou, Fu-chun Lin, Jiong Zhu, et al. Whole brain diffusion tensor imaging histogram analysis in vascular cognitive impairment[J]. Neurological Sciences, 2008, 268(1~2): 60-64.
    [31] Chui HC, Mack W, Jackson JE, et al. Clinical criteria for the diagnosis of vascular dementia: a multicenter study of comparability and inter-rater reliability [J]. Arch Neurol, 2000, 57(2):191-196.
    [32] Erkinjuntti T, Ostbye T, Steenhuis R, Hachinski V. The effect of different diagnostic criteria on the prevalence of dementia[J]. Lancet, 1997,337:1667-1674.
    [33] Rockwood K, Howard K, MacKnisht C, et a1. Spectrum of disease in vascular cognitive impairment [J]. Neuroepidemiology, 1999, 18(5):248-254.
    [34] Ingles JL, Wentzel C, Fisk JD, et al. Neuropsychological predictors of incident dementia in patients with vascular cognitive impairment, without dementia[J]. Stroke, 2002, 22(8):1999-2002.
    [35] Passmore AP, Bayer AJ, Steinhagen-Thiessen E. Cognitive,global, and functional benefits of donepezil in Alzheimer’s disease and vascular dementia: results from large-scale clinical trials[J]. J Neurol Sci, 2005:229-230:141-146.
    [36] Martin D, Hugh SM, Stephen S, et a1.Donepezil in patients with subcortical vascular cognitive impairment: a randomized double-blind trail in CADASIL[J]. Lancet Neurol, 2008, 7(4): 310~318.
    [37] Forette F, Seux ML, Staessen JA, et a1. Prevention of dementia I randomized double- blind placebo-controlled Systolic Hypertension in Europe (Syst-Eur) Trial[J]. Lancet, 1998, 352:1347-1351.
    [38] Firbank MJ, Wiseman RM,Burton EJ, et a1.Brain atrophy and white matter hyperintensity change in older adults and relationships to blood pressure. Brain atrophy, WMH change and blood pressure[J]. J Neurol, 2007, 254:713-721.
    [39] Pantoni L, del Ser T, Soglian AG, et a1. Efficacy and safety of nimodipine in subcortical vascular dementia: a randomized placebo-controlled tria1[J]. Stroke, 2005, 36: 619-624.
    [40] Prince M, Graham N, Brodaty H, et al. Alzheimer disease international’s 10/66 dementia research group-one model for action research in developing countries[J]. Int J Geriatr Psychiatry, 2004,19(2): 178-181.
    [41] Roman GC, Tatemichi TK, Erkinjuntti T, et al. Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop[J]. Neurology, 1993, 43:250-60.
    [42] Chui H. Dementia due to subcortical ischaemic vascular disease[J]. Clin Cornerstone 2001, 3:40-51.
    [43] Wahlund LO, Barkhof F, Fazekas F, Bronge L, Augustin M, Sj?gren M, et al. A New Rating Scale for Age-Related White Matter Changes Applicable to MRI and CT[J]. Stroke 2001,32(6):1318-1322.
    [44] Kapeller P, Barber R, Vermeulen RJ, Adèr H, Scheltens P,et al.Visual Rating of Age-Related White Matter Changes on Magnetic Resonance Imaging: Scale Comparison, Interrater Agreement, and Correlations With Quantitative Measurements[J]. Stroke.2003, 34:441-445.
    [45] Boiten J, Lodder J. Lacunar infarcts: Pathogenesis and validity of the clinical syndromes[J].Stroke, 1991, 22:1374–1378.
    [46] Adams HP Jr, Bendixen BH, Kapelle LJ, et al. Classification of subtype of acute ischemic stroke: Definitions for use in a multicenter clinical trial[J].Stroke, 1993,24:35-41.
    [47] Jackson C, Sudlow C. Are lacunar stroke really different? A systematic review of differences in risk factor profiles between lacunar and nonlacunar infarcts [J]. Stroke, 2005, 36:891-904.
    [48] Rothrock JF, Lyden PD, Hesselink JH, et al.Brain magnetic resonance imaging in the evaluation of lacunar stroke[J].Stroke,1987,18(4):781-786.
    [49]中国高血压防治指南修订委员会. 2004年中国高血压防治指南(实用本)[J].高血压杂志,2004,12(6):483-486.
    [50] Zimmet P, Magliano D, Matsuzawa Y, et al. The metabolic syndrome:a global public health problem and a new definition[J].Journal of Atherosclerosis and Thrombosis,2005, 12(6):295-300.
    [51] Scott MG,James IC,Stephen RD,et al. Diagnosis and management of the metabolic syndrome.An American Heart Association/National Heart, Lung,and Blood Institute Scientific Statement[J]. Circulation, 2005, 112(17): 2735-2752.
    [52] Folstein MF, Folstein SE, McHugh PR. MiniMental State:a practical method for grading the cognitive state of patients for the clinician[J]. J PsychiatrRes, 1975, 12: 189-198.
    [53]张明园精神科评定量表手册[M].长沙:湖南科学技术出版社,1993:122-7,185-9,192-3.
    [54] Nasreddine ZS, Phillip sNA, BedirianV. The Montreal Cognitive Assessment, MoCA:a brief screening tool for mild cognitive impairment[J]. J AmGeriatr Soc. 2005, 53 (4):695-699.
    [55] Adams HP Jr, Davis PH, Leira EC, Chang KC, Bendixen BH, Clarke WR, Woolson RF, Hansen MD. Baseline NIH Stroke Scale score strongly predicts outcome after stroke: A report of the Trial of Org 10172 in Acute Stroke Treatment (TOAST) [J]. Neurology, 1999, 53(1):126-131.
    [56] Mahoney FI, Barthel D. Functional evaluation: the Barthel Index[J]. Maryland State Medical Journal,1965, 14:56-61.
    [57] Hamilton M. The assessment of anxiety by rating scale [J]. Br J MedPsychol, 1959, 32: 50-55.
    [58] Hamilton M.A rating scale for depression [J]. J Neurol Neurosurg Psychiatry, 1960,23:56-62.
    [59] Jorm AF, J acomb PA. The Informant Questionnaire on Cognitive Decline in the Elderly (IQCODE):socio-demographic correlates, reliability, validity and some norms [J]. Psychol Med, 1989,19:1015-1022.
    [60] Donnan GA, Norrving B, Bamford JM, Bogousslavsky J. Classification of subcortical I nfarcts. In: Donnan G, Norrving B, Bamford J, Bogousslavsky J, eds[M]. Subcortical stroke, 2nd edn. Oxford: Oxford Medical Publications, 2002: 27–34.
    [61] HebertR, Brayne C. Epidemiology of vascular dementia [J]. Neuroepidemiology, 1995,4:240-257.
    [62] Nyenhuis DL, Gorelick PB.Vascular dementia: a contemporary review of epidemiology, diagnosis, prevention, and treatment [J]. J Am Geriatr Soc, 1998,46:1437-1448.
    [63] Skoog I. Status of risk factors for vascular dementia [J]. Neuroepidemiology, 1998,17:2.
    [64] Gorelick PB. Status of risk factors for dementia associated with stroke [J]. Stroke, 1997, 28:459- 463.
    [65] Censori B, Manara O, Agostinis C,et al. Dementia after first stroke[J] .Stroke 1996,27:1205 -1210.
    [66]沈沸,李焰生.卒中后痴呆[J].国外医学·脑血疾病分册, 2005,13(9):663-667.
    [67] Bruce DG, Casey GP, Grange VC. Cognitive impairment, physical disability and depressive symptoms in older diabetic patients: the Fremantle Cognition in Diabetes Study[J]. Diabetes Res Clin Pract, 2003, 61(1):59.
    [68] Reitz C, Tang MX, Luchsinger J, et al. Relation of plasma lipids to Alzheimer disease and vascular dementia [J]. Arch Neurol,2004,61:705-714.
    [69] Dufouil C, Richard F, Fievet N, et al. APOE genotype, cholesterol level, lipid-lowering treatment, and dementia: the Three-City Study[J]. Neurology, 2005, 64:1531-1538.
    [70] Irie F, Fitzpatrick AL, Lopez OL, Kuller LH, Peila R, Newman AB, Launer LJ. Enhanced risk for Alzheimer disease in persons with type 2diabetes and APOE e 4[J]. Arch Neurol. 2008, 65: 89-93.
    [71] Schafer JH, Glass TA, Bolla KI, et al . Homocysteine and cognitive function in a population-based study of older adults [J]. J Am Geriatr Soc, 2005, 53 (3): 381-388.
    [72] Vidal J-S, Dufouil C, Ducros V, Tzourio C. Homocysteine, folate, and cognition in a large community-based sample of elderly people-The 3C Dijon Study[J]. Neuroepidemiology, 2008, 30:207–214.
    [73] Garde E, Mortensen EL, Rost rup E, et al . Decline in intelligence is associated wit hprogression in white matter hyperintensity volume[J].J Neurol Neurosurg Psychiatry, 2005,76(9),1289 -1291.
    [74] Magalhaes JP, Sandberg A. Cognitive aging as an extention of brain development: a model linking learning, brain plasticity and neurodegeneration[J]. Mech Ageing Dev,2005,7:57-68.
    [75] AdriàArbox, Josep Lluís, Martí-Vilalta. Lacunar stroke.Expert Rev[J]. Neurother, 2009, 9(2):179-181.
    [76] Erkinjuntti T. Subcortical Vascular dementia[J].Cerebrovasc Dis, 2002,13(2):58-60.
    [77] Jokinen H, Kalska H, Mantyla R, et al. Cognitive profile of subcortical ischaemic vascular disease[J]. J Neurol Neurosurg Psychiatry, 2006, 77:28-33.
    [78] Roman GC, Erkinjuntti T, Wallin A, Pantoni L, Chui HC. Subcortical ischemic vascular dementia[J]. Lacet Neurol, 2002, 1(7):426-436.
    [79]贾建平.临床痴呆病学[M].北京:北京大学医学出版社,2008:16-17.
    [80] Stebbins GT, Nyenhuis DL, Wang C, Cox JL, Freels S, Bangen K,DeToledo-Morrell L, Sripathirathan K, Moseley M, Turner DA, Gabrieli JDE, Gorelick PB.Gray matter atrophy in patients with ischemic stroke with cognitive impairment[J].Stroke, 2008,39:785–793.
    [81] MesulamMM. From sensation to cognition[J].Brain, 1998,121:1013-1052.
    [82] Grau-Olivares M, Arboix A, Bartré-Faz D, JunquéC. Neuropsychological abnormalities associated with lacunar infarction [J].Neurol. Sci, 2007,257:160-165.
    [83] Matthias WR, Silke R, Daniel B, et a1.Screening for cognitive impairment in patients with acute stroke [J]. Dement Geriatr Cogn Disord, 2004,17(8):49-53.
    [84] Kotila M, Waltimo O, Niemi ML, et al .The profile of recovery from stroke and factors influencing outcome [J].Stroke, 1984, 15: 1039-1044.
    [85] Desmond DW, Moroney JT, Sano M, et al. Recovery of cognitive function after stroke [J]. Stroke, 1996, 27(10): 1798-1803.
    [86] Ballard C, Rowan E, Stephens S, et al. Prospective follow- up study between 3 and 15 months after stroke: improvements and decline in cognitive function among dementia-free stroke survivors > 75 years of age [J].Stroke, 2003, 34(10): 2440-2445.
    [87] Wade DT, Hewer RL. Functional abilities after stroke: measurement, natural history and prognosis[J]. J Neurol Neurosurg Psychiatry, 1987,50:177-182.
    [88] Bo Norrving Lacunar infarcts: no black holes in the brain are benign[J]. Pract Neurol 2008:222-228.
    [89] Medina D, DeToledo-Morrell L, Urresta F, et al. White matter changes in mild cognitive impairment and AD: a diffusion tensor imaging study [J]. Neurobiol Aging, 2006,27:663-723.
    [90] Nitkunan A, Barrick TR, Charlton RA, Clark CA, Markus HS. Mul-timodal MRI in cerebralsmall vessel disease: its relationship with cognitionand sensitivity to change over time[J]. Stroke, 2008,39:1999-2005.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700