通过常规肌肉活检检测 pTDP-43:有望成为肌萎缩性脊髓侧索硬化症的诊断生物标志物

IF 5.8 2区 医学 Q1 CLINICAL NEUROLOGY
Brain Pathology Pub Date : 2024-04-11 DOI:10.1111/bpa.13261
Qi-Jie Zhang, Jie Lin, You-Liang Wang, Long Chen, Ying Ding, Fu-Ze Zheng, Huan-Huan Song, Ao-Wei Lv, Yu-Ying Li, Qi-Fu Guo, Min-Ting Lin, Wei Hu, Liu-Qing Xu, Wen-Long Zhao, Ling Fang, Meng-Chao Cui, Zhi-Fei Fu, Wan-Jin Chen, Jing Zhang, Zhi-Qiang Wang, Ning Wang, Ying Fu
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引用次数: 0

摘要

肌萎缩性脊髓侧索硬化症(ALS)是一种破坏性神经退行性疾病,病理特征为 TDP-43 聚集。最近有证据表明,磷酸化 TDP-43(pTDP-43)不仅存在于运动神经元中,也存在于肌肉组织中。然而,目前还不清楚检测肌肉组织中的 pTDP-43 聚集是否有助于 ALS 的诊断。我们提出了三个关键问题:(i) 在常规活检的肌肉中能否检测到 pTDP-43 的聚集? (ii) pTDP-43 聚集的检测能否区分 ALS 和非 ALS 患者?(iii) 能否在 ALS 早期阶段观察到 pTDP-43 聚集?我们进行了一项诊断研究,包括两组:一组是 ALS 组,其中 18 例接受了肌肉活检,这些肌肉活检是从由 802 例 ALS 患者组成的注册 ALS 队列中筛选出来的;另一组是非 ALS 对照组,我们从 684 例患者的生物样本库中随机抽取了 54 份肌肉样本。在18例ALS患者中,3例患者的C9ORF72基因中存在病理GGGGCC重复序列,2例患者的SOD1基因发生突变,7例患者处于早期阶段,只有一个身体区域受到临床影响。在常规活检的肌肉中,包括肱二头肌、三角肌、胫骨前肌和股四头肌,均可检测到 pTDP-43 的聚集。94.4%的肌萎缩性脊髓侧索硬化症患者(17/18)出现 pTDP-43 异常聚集,而非肌萎缩性脊髓侧索硬化症对照组中只有 29.6%的患者(16/54;p < 0.001)出现这种异常聚集。pTDP-43 聚集体主要靠近肌浆膜。我们使用半量化的 pTDP-43 聚集体评分,将 3 作为诊断生物标志物的临界值,结果灵敏度为 94.4%,特异性为 83.3%。此外,我们还观察到 pTDP-43 在临床症状和肌电图病变出现之前就已在肌肉组织中聚集。我们的研究为通过常规肌肉活检检测 pTDP-43 的积累提供了概念验证,它可作为诊断 ALS 的新型生物标记物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis

Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis

Detection of pTDP-43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease, pathologically characterized by TDP-43 aggregates. Recent evidence has been indicated that phosphorylated TDP-43 (pTDP-43) is present not only in motor neurons but also in muscle tissues. However, it is unclear whether testing pTDP-43 aggregation in muscle tissue would assist in the diagnosis of ALS. We propose three key questions: (i) Is aggregation of pTDP-43 detectable in routine biopsied muscles? (ii) Can detection of pTDP-43 aggregation discriminate between ALS and non-ALS patients? (iii) Can pTDP-43 aggregation be observed in the early stages of ALS? We conducted a diagnostic study comprising 2 groups: an ALS group in which 18 cases underwent muscle biopsy screened from a registered ALS cohort consisting of 802 patients and a non-ALS control group, in which we randomly selected 54 muscle samples from a biospecimen bank of 684 patients. Among the 18 ALS patients, 3 patients carried pathological GGGGCC repeats in the C9ORF72 gene, 2 patients carried SOD1 mutations, and 7 patients were at an early stage with only one body region clinically affected. The pTDP-43 accumulation could be detected in routine biopsied muscles, including biceps brachii, deltoid, tibialis anterior, and quadriceps. Abnormal aggregation of pTDP-43 was present in 94.4% of ALS patients (17/18) compared to 29.6% of non-ALS controls (16/54; p < 0.001). The pTDP-43 aggregates were mainly close to the sarcolemma. Using a semi-quantified pTDP-43 aggregates score, we applied a cut-off value of 3 as a diagnostic biomarker, resulting in a sensitivity of 94.4% and a specificity of 83.3%. Moreover, we observed that accumulation of pTDP-43 occurred in muscle tissues prior to clinical symptoms and electromyographic lesions. Our study provides proof-of-concept for the detection of pTDP-43 accumulation via routine muscle biopsy which may serve as a novel biomarker for diagnosis of ALS.

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来源期刊
Brain Pathology
Brain Pathology 医学-病理学
CiteScore
13.20
自引率
3.10%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Brain Pathology is the journal of choice for biomedical scientists investigating diseases of the nervous system. The official journal of the International Society of Neuropathology, Brain Pathology is a peer-reviewed quarterly publication that includes original research, review articles and symposia focuses on the pathogenesis of neurological disease.
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