TDP-43 Proteinopathy Specific Biomarker Development

被引:14
|
作者
Cordts, Isabell [1 ]
Wachinger, Annika [1 ]
Scialo, Carlo [2 ]
Lingor, Paul [1 ,3 ,4 ]
Polymenidou, Magdalini [2 ]
Buratti, Emanuele [5 ]
Feneberg, Emily [1 ]
机构
[1] Tech Univ Munich, Sch Med, Dept Neurol, Klinikum Rechts Isar, D-81675 Munich, Germany
[2] Univ Zurich, Dept Quant Biomed, CH-8057 Zurich, Switzerland
[3] Deutsch Zentrum Neurodegenerat Erkrankungen, DZNE, D-81377 Munich, Germany
[4] Munich Cluster Syst Neurol SyNergy, D-81377 Munich, Germany
[5] Int Ctr Genet Engn & Biotechnol, Mol Pathol, I-34149 Trieste, Italy
关键词
TDP-43; biomarker; neurodegeneration; amyotrophic lateral sclerosis; frontotemporal dementia; dementia; cerebrospinal fluid; biofluid; AMYOTROPHIC-LATERAL-SCLEROSIS; FRONTOTEMPORAL LOBAR DEGENERATION; NEUROFILAMENT LIGHT-CHAIN; C9ORF72 REPEAT EXPANSION; NUCLEAR FACTOR TDP-43; CEREBROSPINAL-FLUID; ALZHEIMERS-DISEASE; RNA-BINDING; POSTTRANSLATIONAL MODIFICATIONS; PHOSPHORYLATED TDP-43;
D O I
10.3390/cells12040597
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
TDP-43 is the primary or secondary pathological hallmark of neurodegenerative diseases, such as amyotrophic lateral sclerosis, half of frontotemporal dementia cases, and limbic age-related TDP-43 encephalopathy, which clinically resembles Alzheimer's dementia. In such diseases, a biomarker that can detect TDP-43 proteinopathy in life would help to stratify patients according to their definite diagnosis of pathology, rather than in clinical subgroups of uncertain pathology. For therapies developed to target pathological proteins that cause the disease a biomarker to detect and track the underlying pathology would greatly enhance such undertakings. This article reviews the latest developments and outlooks of deriving TDP-43-specific biomarkers from the pathophysiological processes involved in the development of TDP-43 proteinopathy and studies using biosamples from clinical entities associated with TDP-43 pathology to investigate biomarker candidates.
引用
收藏
页数:24
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