Wallin Anders, Nordlund Arto, Jonsson Michael, Lind Karin, Edman Åke, Göthlin Mattias, Stålhammar Jacob, Eckerström Marie, Kern Silke, Börjesson-Hanson Anne, Carlsson Mårten, Olsson Erik, Zetterberg Henrik, Blennow Kaj, Svensson Johan, Öhrfelt Annika, Bjerke Maria, Rolstad Sindre, Eckerström Carl
J Cereb Blood Flow Metab. 2016 Jan;36(1):114-31. doi: 10.1038/jcbfm.2015.147.
There is a need for increased nosological knowledge to enable rational trials in Alzheimer’s disease (AD) and related disorders. The ongoing Gothenburg mild cognitive impairment (MCI) study is an attempt to conduct longitudinal in-depth phenotyping of patients with different forms and degrees of cognitive impairment using neuropsychological, neuroimaging, and neurochemical tools. Particular attention is paid to the interplay between AD and subcortical vascular disease, the latter representing a disease entity that may cause or contribute to cognitive impairment with an effect size that may be comparable to AD. Of 664 patients enrolled between 1999 and 2013, 195 were diagnosed with subjective cognitive impairment (SCI), 274 with mild cognitive impairment (MCI), and 195 with dementia, at baseline. Of the 195 (29%) patients with dementia at baseline, 81 (42%) had AD, 27 (14%) SVD, 41 (21%) mixed type dementia (=AD + SVD = MixD), and 46 (23%) other etiologies. After 6 years, 292 SCI/MCI patients were eligible for follow-up. Of these 292, 69 (24%) had converted to dementia (29 (42%) AD, 16 (23%) SVD, 15 (22%) MixD, 9 (13%) other etiologies). The study has shown that it is possible to identify not only AD but also incipient and manifest MixD/SVD in a memory clinic setting. These conditions should be taken into account in clinical trials.
需要增加疾病分类学知识,以便在阿尔茨海默病(AD)及相关疾病中进行合理的试验。正在进行的哥德堡轻度认知障碍(MCI)研究试图使用神经心理学、神经影像学和神经化学工具,对具有不同形式和程度认知障碍的患者进行纵向深入的表型分析。特别关注AD与皮质下血管疾病之间的相互作用,后者是一种疾病实体,可能导致或促成认知障碍,其效应大小可能与AD相当。在1999年至2013年招募的664名患者中,195名在基线时被诊断为主观认知障碍(SCI),274名被诊断为轻度认知障碍(MCI),195名被诊断为痴呆。在基线时患有痴呆的195名(29%)患者中,81名(42%)患有AD,27名(14%)患有SVD,41名(21%)患有混合型痴呆(=AD + SVD = MixD),46名(23%)患有其他病因。6年后,292名SCI/MCI患者符合随访条件。在这292名患者中,69名(24%)已转变为痴呆(29名(42%)为AD,16名(23%)为SVD,15名(22%)为MixD,9名(13%)为其他病因)。该研究表明,在记忆门诊环境中不仅可以识别AD,还可以识别早期和明显的MixD/SVD。在临床试验中应考虑这些情况。