纯霰粒细胞病再探:对边缘、新皮质和纹状体-苍白球-奈杰尔变性的独立影响,以及低度至中度布拉克期系列痴呆症的发展。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Osamu Yokota, Tomoko Miki, Hanae Nakashima-Yasuda, Hideki Ishizu, Takashi Haraguchi, Chikako Ikeda, Masato Hasegawa, Akinori Miyashita, Takeshi Ikeuchi, Naoto Nishikawa, Shintaro Takenoshita, Koichiro Sudo, Seishi Terada, Manabu Takaki
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引用次数: 0

摘要

嗜釉粒细胞(AGs)是一种与年龄相关的肢端病变,在这种病变中,四重复tau选择性积聚。由于之前的研究方法不一,对AGs与痴呆之间关系的研究结果也不一致,因此AGs是否会影响认知功能仍不清楚。为了解决这个问题,我们首先全面评估了30例Braak分期为I-IV期且无其他退行性疾病的纯嗜酸性粒细胞病(pAGD)病例和34例Braak分期为I-IV期且无Aβ沉积或Aβ沉积极少的仅有神经纤维缠结的对照病例中Gallyas阳性AGs的分布和数量以及边缘、新皮层和皮层下区域神经元缺失的严重程度。然后,我们通过多变量有序逻辑回归和二项逻辑回归,研究了AGs对神经元缺失和痴呆是否有独立影响。在30例pAGD病例中,有3例被归类为弥漫型pAGD,即不仅边缘区有明显的神经元缺失,而且新皮层和皮层下核也有明显的神经元缺失。在所有 30 例 pAGD 病例中,随着 Saito AG 阶段的进展,神经元缺失首先出现在杏仁核,其次是颞额叶皮层、海马 CA1、黑质,最后是纹状体和球状苍白球。在对30例pAGD和34例对照病例进行的多变量分析中,斋藤AG期影响了杏仁核、海马CA1、颞额叶皮层、纹状体、球状苍白球和黑质的神经元丢失,而与年龄、Braak期和边缘为主的年龄相关TDP-43脑病(LATE-NC)期无关。在对 23 例 pAGD 和 28 例对照病例(缺乏两个或两个以上裂隙和/或一个或一个以上大面积梗死)进行的多变量分析中,杏仁核(OR 10.02,95% CI 1.12-89.43)和海马 CA1(OR 12.22,95% CI 1.70-87.81),以及颞下部皮质(OR 8.18,95% CI 1.03-65.13)中 AG 的存在对痴呆的影响与年龄、中度 Braak 分期(III-IV)和 LATE-NC 无关。鉴于这些发现,边缘AGs的高密度和颞下回AGs的增加可能会通过神经元丢失导致痴呆症的发生,至少在中低度布拉克阶段的病例中是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stage.

Agyrophilic grains (AGs) are age-related limbic-predominant lesions in which four-repeat tau is selectively accumulated. Because previous methodologically heterogeneous studies have demonstrated inconsistent findings on the relationship between AGs and dementia, whether AGs affect cognitive function remains unclear. To address this question, we first comprehensively evaluated the distribution and quantity of Gallyas-positive AGs and the severity of neuronal loss in the limbic, neocortical, and subcortical regions in 30 cases of pure argyrophilic grain disease (pAGD) in Braak stages I-IV and without other degenerative diseases, and 34 control cases that had only neurofibrillary tangles with Braak stages I-IV and no or minimal Aβ deposits. Then, we examined whether AGs have independent effects on neuronal loss and dementia by employing multivariate ordered logistic regression and binomial logistic regression. Of 30 pAGD cases, three were classified in diffuse form pAGD, which had evident neuronal loss not only in the limbic region but also in the neocortex and subcortical nuclei. In all 30 pAGD cases, neuronal loss developed first in the amygdala, followed by temporo-frontal cortex, hippocampal CA1, substantia nigra, and finally, the striatum and globus pallidus with the progression of Saito AG stage. In multivariate analyses of 30 pAGD and 34 control cases, the Saito AG stage affected neuronal loss in the amygdala, hippocampal CA1, temporo-frontal cortex, striatum, globus pallidus, and substantia nigra independent of the age, Braak stage, and limbic-predominant age-related TDP-43 encephalopathy (LATE-NC) stage. In multivariate analyses of 23 pAGD and 28 control cases that lacked two or more lacunae and/or one or more large infarctions, 100 or more AGs per × 400 visual field in the amygdala (OR 10.02, 95% CI 1.12-89.43) and hippocampal CA1 (OR 12.22, 95% CI 1.70-87.81), and the presence of AGs in the inferior temporal cortex (OR 8.18, 95% CI 1.03-65.13) affected dementia independent of age, moderate Braak stages (III-IV), and LATE-NC. Given these findings, the high density of limbic AGs and the increase of AGs in the inferior temporal gyrus may contribute to the occurrence of dementia through neuronal loss, at least in cases in a low to moderate Braak stage.

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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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