Rozzini Luca, Chilovi Barbara Vicini, Conti Marta, Bertoletti Erik, Delrio Ilenia, Trabucchi Marco, Padovani Alessandro
Department of Neurology, University of Brescia, Italy.
Int J Geriatr Psychiatry. 2007 Dec;22(12):1217-22. doi: 10.1002/gps.1816.
Mild Cognitive Impairment defines a transitional stage between normal ageing and dementia, and reflects the clinical situation where a person has memory complaints and objective evidence of cognitive impairment but no evidence of dementia. To plan the care of patients with MCI, it is important to predict as accurately as possible potential risk factors modulating the conversion to AD.
To investigate the risk factors associated of conversion to dementia of Alzheimer type (AD) for subjects with amnestic Mild Cognitive Impairment (aMCI).
One hundred nineteen subjects consecutively recruited who met the operational criteria for aMCI (with or without deficits in other cognitive domains). They underwent multidimensional assessment and a neuropsychological battery at baseline and at follow-up, after 1 year. Diagnosis for dementia was based on a deficit in two or more cognitive domains severe enough to affect the participant functional abilities. Subjects converted to AD over time were classified as Demented; subjects that remained unchanged, or became cognitively normal during follow-up, were defined as Stable.
Demented MCI (N = 40; 33.6%) were older (mean age 73.5 +/- 8.5 vs. 69.2 +/- 7.0; p = 0.006) when compared to Stable (N = 79; 66.4) and their global cognitive performances, at baseline, were more compromised when assessed by ADAS-Cog (mean score 10.7 +/- 3.9 vs 6.7 +/- 3.4; p = .000) and by MMSE (mean score 26.1 +/- 1.9 vs. 27.3 +/- 1.8; p = 0.002). Demented were similarly compromised in basic activities of daily living (BADL mean 0.2 +/- 0.4 vs 0.1 +/- 0.3 functions lost; p = NS) but more compromised on instrumental daily functions (IADL mean 0.7 +/- 0.8 vs. 0.1 +/- 0.5 functions lost; p = 0.001). The presence of white matter lesions (WML) on CT or MRI was more pronounced in Demented group (p = 0.02). After 1 year; Demented worsened on phonemic verbal fluency (PFL) (p = 0.009), Raven's coloured matrices (p = 0.003), Trail Making test A and B (p = 0.008 and p = 0.007 respectively) and in Instrumental Activities of Daily Living (IADL) (p =0 .000) respect to Stable. Logistic regression analysis revealed that ADAS-Cog basal score, Trail Making B, IADL but not memory deterioration were significantly associated to the conversion to AD.
In subjects with aMCI poor global cognitive performance at baseline, the worsening on executive functions and on functional status but not the worsening on memory functions are independently associated with the conversion to dementia of Alzheimer type at 1 year, follow-up.
轻度认知障碍定义了正常衰老与痴呆之间的过渡阶段,反映了一个人有记忆主诉且有认知障碍的客观证据但无痴呆证据的临床情况。为了规划轻度认知障碍患者的护理,尽可能准确地预测调节向阿尔茨海默病转化的潜在风险因素很重要。
研究遗忘型轻度认知障碍(aMCI)患者转化为阿尔茨海默病型痴呆(AD)的相关危险因素。
连续招募了119名符合aMCI操作标准(有或无其他认知领域缺陷)的受试者。他们在基线和1年后随访时接受了多维评估和神经心理测验。痴呆的诊断基于两个或更多认知领域的缺陷严重到足以影响参与者的功能能力。随时间转化为AD的受试者被归类为痴呆组;在随访期间保持不变或认知恢复正常的受试者被定义为稳定组。
与稳定组(N = 79;66.4%)相比,痴呆型MCI(N = 40;33.6%)年龄更大(平均年龄73.5±8.5岁对69.2±7.0岁;p = 0.006),并且在基线时,通过阿尔茨海默病评定量表认知部分(ADAS-Cog)(平均得分10.7±3.9对6.7±3.4;p = 0.000)和简易精神状态检查表(MMSE)(平均得分26.1±1.9对27.3±1.8;p = 0.002)评估时,他们的整体认知表现受损更严重。痴呆组在基本日常生活活动(BADL)方面同样受损(平均0.2±0.4对0.1±0.3项功能丧失;p =无显著差异),但在工具性日常生活功能(IADL)方面受损更严重(平均0.7±0.8对0.1±0.5项功能丧失;p = 0.001)。痴呆组在CT或MRI上白质病变(WML)的存在更明显(p = 0.02)。1年后;与稳定组相比,痴呆组在音素言语流畅性(PFL)(p = 0.009)、瑞文彩色推理测验(p = 0.003)、连线测验A和B(分别为p = 0.008和p = 0.007)以及工具性日常生活活动(IADL)(p = 0.000)方面恶化。逻辑回归分析显示,ADAS-Cog基础得分、连线测验B、IADL而非记忆恶化与转化为AD显著相关。
在aMCI受试者中,基线时整体认知表现较差,执行功能和功能状态恶化但记忆功能未恶化与1年随访时转化为阿尔茨海默病型痴呆独立相关。