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随机森林模型表明,小胶质细胞和蛋白质错误折叠特征是 C9orf72-ALS 的关键表型标志物。

Random forest modelling demonstrates microglial and protein misfolding features to be key phenotypic markers in C9orf72-ALS.

机构信息

Translational Neuroscience PhD Programme, Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

出版信息

J Pathol. 2022 Dec;258(4):366-381. doi: 10.1002/path.6008. Epub 2022 Oct 20.

DOI:10.1002/path.6008
PMID:36070099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9827842/
Abstract

Clinical heterogeneity observed across patients with amyotrophic lateral sclerosis (ALS) is a known complicating factor in identifying potential therapeutics, even within cohorts with the same mutation, such as C9orf72 hexanucleotide repeat expansions (HREs). Thus, further understanding of pathways underlying this heterogeneity is essential for appropriate ALS trial stratification and the meaningful assessment of clinical outcomes. It has been shown that both inflammation and protein misfolding can influence ALS pathogenesis, such as the manifestation or severity of motor or cognitive symptoms. However, there has yet to be a systematic and quantitative assessment of immunohistochemical markers to interrogate the potential relevance of these pathways in an unbiased manner. To investigate this, we extensively characterised features of commonly used glial activation and protein misfolding stains in thousands of images of post-mortem tissue from a heterogeneous cohort of deeply clinically profiled patients with a C9orf72 HRE. Using a random forest model, we show that microglial staining features are the most accurate classifiers of disease status in our panel and that clinicopathological relationships exist between microglial activation status, TDP-43 pathology, and language dysfunction. Furthermore, we detected spatially resolved changes in fused in sarcoma (FUS) staining, suggesting that liquid-liquid phase shift of this aggregation-prone RNA-binding protein may be important in ALS caused by a C9orf72 HRE. Interestingly, no one feature alone significantly impacted the predictiveness of the model, indicating that the collective examination of all features, or a combination of several features, is what allows the model to be predictive. Our findings provide further support to the hypothesis of dysfunctional immune regulation and proteostasis in the pathogenesis of C9-ALS and provide a framework for digital analysis of commonly used neuropathological stains as a tool to enrich our understanding of clinicopathological relationships within and between cohorts. © 2022 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

摘要

在肌萎缩侧索硬化症(ALS)患者中观察到的临床异质性是识别潜在治疗方法的一个已知复杂因素,即使在具有相同突变(如 C9orf72 六核苷酸重复扩增(HRE))的队列中也是如此。因此,进一步了解导致这种异质性的途径对于适当的 ALS 试验分层和对临床结果的有意义评估至关重要。已经表明,炎症和蛋白质错误折叠都可以影响 ALS 的发病机制,例如运动或认知症状的表现或严重程度。然而,迄今为止,还没有系统和定量评估免疫组织化学标志物,以无偏倚的方式探究这些途径的潜在相关性。为了研究这一点,我们广泛描述了在具有 C9orf72 HRE 的异质临床特征患者队列的数千张死后组织图像中常用的神经胶质激活和蛋白质错误折叠染色的特征。使用随机森林模型,我们表明,小胶质细胞染色特征是我们面板中疾病状态的最准确分类器,并且微胶质细胞激活状态、TDP-43 病理学和语言功能障碍之间存在临床病理关系。此外,我们检测到融合肉瘤(FUS)染色的空间分辨变化,表明这种易聚集 RNA 结合蛋白的液-液相转变可能在由 C9orf72 HRE 引起的 ALS 中很重要。有趣的是,没有一个单一特征对模型的预测性有显著影响,这表明对所有特征的集体检查,或几个特征的组合,是使模型具有预测性的原因。我们的研究结果进一步支持了 C9-ALS 发病机制中免疫调节和蛋白质稳态功能障碍的假说,并为常用神经病理学染色的数字分析提供了一个框架,作为一种工具来丰富我们对队列内和队列间临床病理关系的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abeb/9827842/06f47d089020/PATH-258-366-g001.jpg
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