Disentangling the heterogeneity of multiple sclerosis through identification of independent neuropathological dimensions

IF 9.3 1区 医学 Q1 CLINICAL NEUROLOGY Acta Neuropathologica Pub Date : 2024-05-21 DOI:10.1007/s00401-024-02742-w
Alyse de Boer, Aletta M. R. van den Bosch, Nienke J. Mekkes, Nina L. Fransen, Ekaterina Dagkesamanskaia, Eric Hoekstra, Jörg Hamann, Joost Smolders, Inge Huitinga, Inge R. Holtman
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Abstract

Multiple sclerosis (MS) is a heterogeneous neurological disorder with regards to clinical presentation and pathophysiology. Here, we investigated the heterogeneity of MS by performing an exploratory factor analysis on quantitative and qualitative neuropathology data collected for 226 MS donors in the Netherlands Brain Bank autopsy cohort. Three promising dimensions were identified and subsequently validated with clinical, neuropathological, and genetic data. Dimension 1 ranged from a predominance of remyelinated and inactive lesions to extensive pathological changes, higher proportions of active and mixed lesions, and foamy microglia morphology. This pattern was positively correlated with more severe disease, the presence of B and T cells, and neuroaxonal damage. Scoring high on dimension 2 was associated with active lesions, reactive sites, and the presence of nodules. These donors had less severe disease, a specific pattern of cortical lesions, and MS risk variants in the human leukocyte antigen region, the latter indicating a connection between disease onset and this neuropathological dimension. Donors scoring high on dimension 3 showed increased lesional pathology with relatively more mixed and inactive lesions and ramified microglia morphology. This pattern was associated with longer disease duration, subpial cortical lesions, less involvement of the adaptive immune system, and less axonal damage. Taken together, the three dimensions may represent (1) demyelination and immune cell activity associated with pathological and clinical progression, (2) microglia (re)activity and possibly lesion initiation, and (3) loss of lesion activity and scar formation. Our findings highlight that a thorough understanding of the interplay between multiple pathological characteristics is crucial to understand the heterogeneity of MS pathology, as well as its association with genetic predictors and disease outcomes. The scores of donors on the dimensions can serve as an important starting point for further disentanglement of MS heterogeneity and translation into observations and interventions in living cohorts with MS.

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通过识别独立的神经病理学维度,厘清多发性硬化症的异质性。
多发性硬化症(MS)在临床表现和病理生理学方面是一种异质性神经系统疾病。在此,我们通过对荷兰脑库尸检队列中 226 名多发性硬化症供体的定量和定性神经病理学数据进行探索性因子分析,研究了多发性硬化症的异质性。结果发现了三个有前景的维度,并随后通过临床、神经病理学和遗传学数据进行了验证。维度 1 的范围从再髓鞘化和非活动性病变为主到广泛的病理变化、较高比例的活动性和混合性病变以及泡沫状小胶质细胞形态。这种模式与更严重的疾病、B 细胞和 T 细胞的存在以及神经轴损伤呈正相关。维度 2 的高分与活动性病变、反应性部位和结节的存在有关。这些捐献者的病情较轻,皮质病变模式特殊,人类白细胞抗原区域存在多发性硬化症风险变异,后者表明发病与这一神经病理学维度有关。在维度3上得分较高的供体表现出更多的病变病理,混合性和非活动性病变相对较多,小胶质细胞形态呈横纹状。这种模式与较长的病程、皮质下病变、较少的适应性免疫系统参与和较少的轴突损伤有关。综合来看,这三个维度可能代表(1)与病理和临床进展相关的脱髓鞘和免疫细胞活动,(2)小胶质细胞(再)活动和可能的病变启动,以及(3)病变活动消失和瘢痕形成。我们的研究结果突出表明,透彻了解多种病理特征之间的相互作用对于了解多发性硬化症病理的异质性及其与遗传预测因素和疾病预后的关联至关重要。捐献者在这些维度上的得分可以作为一个重要的起点,进一步揭示多发性硬化症的异质性,并将其转化为对多发性硬化症患者群体的观察和干预。
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来源期刊
Acta Neuropathologica
Acta Neuropathologica 医学-病理学
CiteScore
23.70
自引率
3.90%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Acta Neuropathologica publishes top-quality papers on the pathology of neurological diseases and experimental studies on molecular and cellular mechanisms using in vitro and in vivo models, ideally validated by analysis of human tissues. The journal accepts Original Papers, Review Articles, Case Reports, and Scientific Correspondence (Letters). Manuscripts must adhere to ethical standards, including review by appropriate ethics committees for human studies and compliance with principles of laboratory animal care for animal experiments. Failure to comply may result in rejection of the manuscript, and authors are responsible for ensuring accuracy and adherence to these requirements.
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