期刊文献+

阿尔茨海默病合并白质病变患者的认知功能障碍特点分析 被引量:2

Charactistics of cognitive impairment in the patients with both Alzheimer disease and white matter lesions
下载PDF
导出
摘要 目的探讨阿尔茨海默病(AD)合并白质病变(WML)患者危险因素和认知功能障碍特点。方法临床收集轻度阿尔茨海默病患者77例,根据MRIT2加权像是否合并WML分为单纯AD组34例和阿尔茨海默病合并WML组43例,以78名年龄和教育程度相匹配的认知正常老年人为对照组,分别进行MMSE、数字广度测验、词语延迟回忆测验、词语流畅性测验、积木测验和画钟测验。结果 (1)与对照组和单纯AD病组相比,AD合并WML组高血压病和房颤的比例明显升高(P<0.05)。(2)与对照组相比,单纯AD组和AD合并WML组MMSE、数字广度测验、词语延迟回忆测验、词语流畅性测验、积木测验和画钟测验评分均明显降低(P<0.05)。(3)与单纯AD组相比,AD合并WML组词语流畅性测验、积木测验和画钟测验评分均显著降低(P<0.05)。结论高血压病、糖尿病和房颤可能是AD合并WML的危险因素;WML可加重AD患者视空间和执行功能障碍。 Objective To investigate the characteristics of vascular risks and cognitive impairments in the patients with both Alzheimer disease(AD)and white matter lesions(WML).Methods 77 mild AD patients were classified into pure AD group and AD with WML group according to MRI.78 old individuals with normal cognition were regarded as controll group.All patients'cognitive status were assessed with MMSE,digit span test,auditory verbal delayed memory test,word fluency test,block-test and clock-drawing test.Results ① The prevalence of hypertention and atrial fibrilation in AD with WML group increased significantly than those in pure AD group and control group.② Compared with control group,the patients in pure AD group and in AD with WML group had lower scores in MMSE,digit span test,auditory verbal delayed memory test,word fluency test,block-test and clock-drawing test.③ Compared with pure AD group,the patients in AD with WML group had lower scores in word fluency test,block-test and clock-drawing test.Conclusion Hypertention,diabetes mellitus and atrial fibrilation may be the risk factors of the patients with both AD and WML.WML may promote visual-spatial and executive impairment
出处 《脑与神经疾病杂志》 2010年第3期227-230,共4页 Journal of Brain and Nervous Diseases
关键词 阿尔茨海默病 痴呆 白质 认知功能 Alzheimer disease Dementia White matter Cognitive function
  • 相关文献

参考文献15

  • 1Napoli C,Palinski W.Neurodegenerative diseases:insights into pathogenic mechanisms from atherosclerosis.Neurobiol Aging,2005,26:293-302.
  • 2Stenset V,Johnsen L,Kocot D,et al.Associations between white matter lesions,cerebrovascular risk factors and low CSF Abeta42.Neurology,2006,67:830-833.
  • 3Vermeer SE,Prins ND,den Heijer T,et al.Silent brain infarcts and the risk of dementia and cognitive decline.N Engl J Med,2003,348:1215-1222.
  • 4Prins ND,van Dijk EJ,den Heijer T,et al.Cerebral white matter lesions and the risk of dementia.Arch Neurol,2004,61:1531-1534.
  • 5Fazekas F,Kleinert R,Offenbacher H,et al.Pathologic correlates of incidental MRI white matter signal hyperintensities.Neurology,1993,43:1683-1689.
  • 6Kapeller P,Barber R,Vermeulen RJ,et al.Visual rating of age-related white matter changes on magnetic resonance Imaging.scale comparison,interrater agreement,and correlations with quantitative measurements.Stroke,2003,34:441-445.
  • 7Gold G,Kovari E,Herrmann FR,et al.Cognitive consequences of thalamic,basal ganglia,and deep white matter lacunes in brain aging and dementia.Stroke,2005,36:1184-1188.
  • 8Luchsinger JA,Reitz C,Honig LS,et al.Aggregation of vascular risk factors and risk of incident Alzheimer disease.Neurology,2005,65:545-551.
  • 9Riekse RG,Leverenz JB,McCormick W,et al.Effect of vascular lesions on cognition in Alzheimer's disease:a community-based study.J Am Geriatr Soc,2004,52:1442-1448.
  • 10Jellinger KA,Mitter-Ferstl E.The impact of cerebrovascular lesions in Alzheimer disease--a comparative autopsy study.J Neurol,2003,250:1050-1055.

同被引文献24

  • 1Noth U,Rackwitz L,Heymer A,et al.Chondrogenicdifferentiation of human mesenchymal stem cells in collagen typeⅠhydrogels.J Biomed Mater Res A,2007,83(3):626-635.
  • 2Briggs T,Treiser MD,Holmes PF,et al.Osteogenicdifferentiation of human mesenchymal stem cells on poly(ethyleneglycol)-variant biomaterials.J Biomed Mater Res A,2009,91(4):975-984.
  • 3Lin W,Chen X,Wang X,et al.Adult rat bone marrow stromal cells differentiate into Schwann cell-like cells in vitro.In Vitro Cell Dev Biol Anim,2008,44(1-2):31-40.
  • 4Watanabe T,Yamagata N,Takasaki K,et al.Decreased acetylcholine release is correlated to memory impairment in the Tg2576 transgenic mouse model of Alzheimer's disease.Brain Res,2009,1249:222-228.
  • 5Katharina Schindowski Zimmermann.Decreased axonal transport during Alzheimer's-like spatial-temporal tau pathology leads to imbalance of NGF,cholinergicdysfunction,and decreased regulation of BDNF and TrkB.Alzheimer's and Dementia,2011,7(4):S560-S561.
  • 6Madziar B,Shah S,Brock M,et al.Nerve growth factor regulates the expression of the cholinergiclocus and the high-affinity choline transporter via the Akt/PKB signaling pathway.J Neurochem,2008, 107(5):1284-1293.
  • 7Chaldakov GN,Tonchev AB,Aloe L.NGF and BDNF:from nerves toadi pose tissue,from neurokines to metabokines.Riv Psichiatr,2009, 44(2):79-87.
  • 8Nilbratt M,Porras O,Marutle A,et al.Neurotrophicfactors promote cholinergicdifferentiation in human embryonicstem cell-derived neurons.J Cell Mol Med,2010,14(6B):1476-1484.
  • 9Reilly JO,Karavanova ID,Williams KP,et al.Cooperrative effects of Sonic Hedgehog and NGF on basal forebrain chol inergic neurons.Mol Cell Neurosci,2002,19(1):88-96.
  • 10王小洁,彭清,徐勇.高血压病患者认知功能与胰岛素抵抗的相关性研究[J].临床荟萃,2008,23(6):393-396. 被引量:8

引证文献2

二级引证文献23

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部