制定、评估、验证和实施用于评估死后脑组织中脑淀粉样血管病的共识协议。

American journal of neurodegenerative disease Pub Date : 2014-03-28 eCollection Date: 2014-01-01
Seth Love, Katy Chalmers, Paul Ince, Margaret Esiri, Johannes Attems, Kurt Jellinger, Masahito Yamada, Mark McCarron, Thais Minett, Fiona Matthews, Steven Greenberg, David Mann, Patrick Gavin Kehoe
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引用次数: 0

摘要

在一个由 11 个对脑淀粉样血管病(CAA)有研究兴趣的团体参与的合作项目中,我们分两个阶段制定并验证了一个新的共识方案和评分计划,用于评估死后脑组织中的 CAA 和相关血管病理学异常。第一阶段采用德尔菲式迭代调查来制定共识方案。由此产生的评分方案在一系列数字图像和石蜡切片上进行了测试,这些数字图像和石蜡切片在一些评分者之间盲传。通过公开论坛讨论,对评分方案和染色方法的选择进行了完善。商定的方案以 0-3 级对实质和脑膜 CAA 进行评分,以 0-2 级对毛细血管 CAA 的存在/不存在和血管病变进行评分,4 个皮质叶分别进行评分。随后,三个中心参与了进一步的评估。三个中心(布里斯托尔、牛津和谢菲尔德)的神经病理学家对 75 个病例(每个中心 25 个)的切片进行了独立评分,结果显示评分者之间的可靠性很高。第二阶段利用三个中心的评估结果,通过研究之前描述过的 APOE 基因型(之前已确定)与 CAA 和血管病变之间的关联,对方案进行验证。毛细血管 CAA(伴有或不伴有动脉 CAA)与 APOE ε4 的关系得到了证实。然而,APOE ε2也被认为是发生CAA的一个强有力的危险因素,不仅在AD患者中如此,在非痴呆老年对照组中也是如此。我们鼓励对该方案和评分计划进行进一步验证,以帮助其被更广泛地采用,促进CAA的合作研究和复制研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development, appraisal, validation and implementation of a consensus protocol for the assessment of cerebral amyloid angiopathy in post-mortem brain tissue.

Development, appraisal, validation and implementation of a consensus protocol for the assessment of cerebral amyloid angiopathy in post-mortem brain tissue.

Development, appraisal, validation and implementation of a consensus protocol for the assessment of cerebral amyloid angiopathy in post-mortem brain tissue.

In a collaboration involving 11 groups with research interests in cerebral amyloid angiopathy (CAA), we used a two-stage process to develop and in turn validate a new consensus protocol and scoring scheme for the assessment of CAA and associated vasculopathic abnormalities in post-mortem brain tissue. Stage one used an iterative Delphi-style survey to develop the consensus protocol. The resultant scoring scheme was tested on a series of digital images and paraffin sections that were circulated blind to a number of scorers. The scoring scheme and choice of staining methods were refined by open-forum discussion. The agreed protocol scored parenchymal and meningeal CAA on a 0-3 scale, capillary CAA as present/absent and vasculopathy on 0-2 scale, in the 4 cortical lobes that were scored separately. A further assessment involving three centres was then undertaken. Neuropathologists in three centres (Bristol, Oxford and Sheffield) independently scored sections from 75 cases (25 from each centre) and high inter-rater reliability was demonstrated. Stage two used the results of the three-centre assessment to validate the protocol by investigating previously described associations between APOE genotype (previously determined), and both CAA and vasculopathy. Association of capillary CAA with or without arteriolar CAA with APOE ε4 was confirmed. However APOE ε2 was also found to be a strong risk factor for the development of CAA, not only in AD but also in elderly non-demented controls. Further validation of this protocol and scoring scheme is encouraged, to aid its wider adoption to facilitate collaborative and replication studies of CAA.

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