Bibliographic Details
| Title: |
Detection of pTDP‐43 via routine muscle biopsy: A promising diagnostic biomarker for amyotrophic lateral sclerosis. |
| Authors: |
Zhang, Qi‐Jie, Lin, Jie, Wang, You‐Liang, Chen, Long, Ding, Ying, Zheng, Fu‐Ze, Song, Huan‐Huan, Lv, Ao‐Wei, Li, Yu‐Ying, Guo, Qi‐Fu, Lin, Min‐Ting, Hu, Wei, Xu, Liu‐Qing, Zhao, Wen‐Long, Fang, Ling, Cui, Meng‐Chao, Fu, Zhi‐Fei, Chen, Wan‐Jin, Zhang, Jing, Wang, Zhi‐Qiang |
| Source: |
Brain Pathology; Nov2024, Vol. 34 Issue 6, p1-13, 13p |
| Subject Terms: |
BICEPS brachii, TIBIALIS anterior, MOTOR neurons, NEURODEGENERATION, QUADRICEPS muscle, AMYOTROPHIC lateral sclerosis |
| Abstract: |
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. [ABSTRACT FROM AUTHOR] |
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| Database: |
Complementary Index |
