Okello A, Koivunen J, Edison P, Archer H A, Turkheimer F E, Någren K, Bullock R, Walker Z, Kennedy A, Fox N C, Rossor M N, Rinne J O, Brooks D J
Division of Neuroscience and Mental Health, Faculty of Medicine, Imperial College London, UK.
Neurology. 2009 Sep 8;73(10):754-60. doi: 10.1212/WNL.0b013e3181b23564. Epub 2009 Jul 8.
Patients with amnestic mild cognitive impairment (MCI) represent an important clinical group as they are at increased risk of developing Alzheimer disease (AD). (11)C-PIB PET is an in vivo marker of brain amyloid load.
To assess the rates of conversion of MCI to AD during a 3-year follow-up period and to compare levels of amyloid deposition between MCI converters and nonconverters.
Thirty-one subjects with MCI with baseline (11)C-PIB PET, MRI, and neuropsychometry have been clinically followed up for 1 to 3 years (2.68 +/- 0.6 years). Raised cortical (11)C-PIB binding in subjects with MCI was detected with region of interest analysis and statistical parametric mapping.
Seventeen of 31 (55%) subjects with MCI had increased (11)C-PIB retention at baseline and 14 of these 17 (82%) clinically converted to AD during follow-up. Only one of the 14 PIB-negative MCI cases converted to AD. Of the PIB-positive subjects with MCI, half (47%) converted to AD within 1 year of baseline PIB PET, these faster converters having higher tracer-retention values than slower converters in the anterior cingulate (p = 0.027) and frontal cortex (p = 0.031). Seven of 17 (41%) subjects with MCI with known APOE status were epsilon4 allele carriers, this genotype being associated with faster conversion rates in PIB-positive subjects with MCI (p = 0.035).
PIB-positive subjects with mild cognitive impairment (MCI) are significantly more likely to convert to AD than PIB-negative patients, faster converters having higher PIB retention levels at baseline than slower converters. In vivo detection of amyloid deposition in MCI with PIB PET provides useful prognostic information.
遗忘型轻度认知障碍(MCI)患者是一个重要的临床群体,因为他们患阿尔茨海默病(AD)的风险增加。(11)C-PIB PET是脑淀粉样蛋白负荷的一种体内标志物。
评估3年随访期内MCI转化为AD的发生率,并比较MCI转化者和未转化者之间的淀粉样蛋白沉积水平。
对31例具有基线(11)C-PIB PET、MRI和神经心理测量的MCI患者进行了1至3年(2.68±0.6年)的临床随访。通过感兴趣区分析和统计参数映射检测MCI患者皮质(11)C-PIB结合升高情况。
31例MCI患者中有17例(55%)在基线时(11)C-PIB滞留增加,这17例中的14例(82%)在随访期间临床转化为AD。14例PIB阴性的MCI病例中只有1例转化为AD。在PIB阳性的MCI受试者中,一半(47%)在基线PIB PET检查后1年内转化为AD,这些转化较快者在前扣带回(p = 0.027)和额叶皮质(p = 0.031)的示踪剂滞留值高于转化较慢者。17例已知APOE状态的MCI患者中有7例(41%)是ε4等位基因携带者,该基因型与PIB阳性的MCI患者更快的转化率相关(p = 0.035)。
PIB阳性的轻度认知障碍(MCI)患者比PIB阴性患者更有可能转化为AD,转化较快者在基线时的PIB滞留水平高于转化较慢者。用PIB PET对MCI患者进行淀粉样蛋白沉积的体内检测可提供有用的预后信息。